Selección de Resúmenes de Menopausia

Semana del 27 de Agosto al 02 de Septiembre 2008

Juan Enrique Blümel. Departamento Medicina Sur. Universidad de Chile

 

 

 

 

 

Menopause. 2008 Aug 26. [Epub ahead of print]

Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy.

Rocca WA, Grossardt BR, Geda YE, Gostout BS, Bower JH, Maraganore DM, de Andrade M,

From the Divisions of 1Epidemiology and 2Biostatistics, Department of Health Sciences Research; Departments of 3Psychiatry and Psychology, 4Obstetrics and Gynecology, and 5Neurology, College of Medicine, Mayo Clinic, Rochester, MN.

OBJECTIVE:: We studied the long-term risk of depressive and anxiety symptoms in women who underwent bilateral oophorectomy before menopause. DESIGN:: We conducted a cohort study among all women residing in Olmsted County, MN, who underwent bilateral oophorectomy before the onset of menopause for a noncancer indication from 1950 through 1987. Each member of the bilateral oophorectomy cohort was matched by age with a referent woman from the same population who had not undergone an oophorectomy. In total, we studied 666 women with bilateral oophorectomy and 673 referent women. Women were followed for a median of 24 years, and depressive and anxiety symptoms were assessed using a structured questionnaire via a direct or proxy telephone interview performed from 2001 through 2006. RESULTS:: Women who underwent bilateral oophorectomy before the onset of menopause had an increased risk of depressive symptoms diagnosed by a physician (hazard ratio = 1.54, 95% CI: 1.04-2.26, adjusted for age, education, and type of interview) and of anxiety symptoms (adjusted hazard ratio = 2.29, 95% CI: 1.33-3.95) compared with referent women. The findings remained consistent after excluding depressive or anxiety symptoms that first occurred within 10 years after oophorectomy. The associations were greater with younger age at oophorectomy but did not vary across indications for the oophorectomy. In addition, treatment with estrogen to age 50 years in women who underwent bilateral oophorectomy at younger ages did not modify the risk. CONCLUSIONS:: Bilateral oophorectomy performed before the onset of menopause is associated with an increased long-term risk of depressive and anxiety symptoms.

 

 

Menopause. 2008 Aug 21. [Epub ahead of print]

Effect of progestogen and progestogen type on hemostasis measures in postmenopausal women: the Postmenopausal Estrogen/Progestin Intervention (PEPI) Study.

Smith NL, Wiley JR, Legault C, Rice KM, Heckbert SR, Psaty BM, Tracy RP, Cushman M.

From the Departments of 1Epidemiology, 2Medicine, 3Biostatistics, and 4Health Services, University of Washington, Seattle, WA; 5Seattle Epidemiologic Research and Information Center of the Department of Veterans Affairs Office of Research and Development, Seattle, WA; 6Department of Public Health Sciences, Wake Forest University, Winston-Salem, NC; and 7Departments of Pathology and Laboratory Medicine, University of Vermont, Burlington, VT.

OBJECTIVE:: The contribution of progestogen therapy or progestogen type to risks and benefits of estrogen treatment is inadequately characterized. We examined the effect of conjugated equine estrogens (CEE) with and without concomitant progestogen treatments on changes in hemostasis measures among Postmenopausal Estrogen/Progestin Intervention participants. DESIGN:: Postmenopausal Estrogen/Progestin Intervention was a clinical trial that randomized 875 postmenopausal women to one of five arms: placebo, CEE alone, CEE with cyclic micronized progesterone (MP), CEE with cyclic medroxyprogesterone acetate (MPA), and CEE with continuous MPA. Twelve hemostasis assays were measured in a substudy at baseline and 12 and 36 months. Using 12- and 36-month changes in hemostasis measures, we calculated change ratios for two comparisons of active treatments: CEE+MPA versus CEE and CEE+MPA versus CEE+MP. RESULTS:: Hemostasis measures were available for 288 women. Compared with women assigned to CEE alone, 12-month increases in factor VIIc and protein C among women assigned to CEE+MPA were relatively smaller (ratios: 0.94 [95% CI: 0.89-0.98] and 0.96 [95% CI: 0.92-1.00]), respectively. Compared with women assigned to CEE+MP, women assigned to CEE+MPA had smaller increases in factor VIIc and larger decreases in plasminogen activator inhibitor-1 antigen at 12 months (ratios: 0.94 [95% CI: 0.90-0.98] and 0.70 [95% CI: 0.53-0.93], respectively). Thirty-six month ratios were similar to these. Women assigned to CEE+MPA had smaller increases in protein C than those assigned CEE+MP at 36 months only (ratio: 0.95 [95% CI: 0.91-0.99]). No other associations were significant. CONCLUSIONS:: We found modest yet significant differences in hemostasis measure changes when comparing progestogen use and progestogen type in postmenopausal women using CEE.

 

 

Cancer Epidemiol Biomarkers Prev. 2008 Aug 25. [Epub ahead of print]

Estrogen plus Progestin and Risk of Benign Proliferative Breast Disease.

Rohan TE, Negassa A, Chlebowski RT, Lasser NL, McTiernan A, Schenken RS, Ginsberg M, Wassertheil-Smoller S, Page DL.

Albert Einstein College of Medicine, Bronx, New York; Harbor-UCLA Medical Center, Torrance, California; New Jersey Medical School, Newark, New Jersey; Fred Hutchinson Cancer Research Center, Seattle, Washington; University of Texas Health Science Center, San Antonio, Texas; and Vanderbilt University Medical School, Nashville, Tennessee.

Women with benign proliferative breast disease are at increased risk of subsequent breast cancer. Estrogens and progesterone exert proliferative effects on mammary epithelium, and combined hormone replacement therapy has been associated with increased breast cancer risk. We tested the effect of conjugated equine estrogen plus progestin on the risk of benign proliferative breast disease in the Women's Health Initiative (WHI) randomized controlled trial. In the WHI trial of estrogen plus progestin, 16,608 postmenopausal women were randomly assigned either to 0.625 mg/day of conjugated equine estrogen plus 2.5 mg/day of medroxyprogesterone acetate or to placebo. Baseline and annual breast exams and mammograms were required. The trial was terminated early (average follow-up, 5.5 years). We identified women who had had a biopsy for benign breast disease, and subjected histologic sections from the biopsies to standardized review. Overall, 178 incident cases of benign proliferative breast disease were ascertained in the estrogen plus progestin group and 99 in the placebo group. The use of estrogen plus progestin was associated with a 74% increase in the risk of benign proliferative breast disease [hazard ratio, 1.74; 95% confidence interval (CI), 1.35-2.25]. For benign proliferative breast disease without atypia the hazard ratio was 2.00 (95% CI, 1.50-2.66), while for atypical hyperplasia it was 0.76 (95% CI, 0.38-1.52). The risk varied little by levels of baseline characteristics. The results of this study suggest that the use of estrogen plus progestin may increase the risk of benign proliferative breast disease.

 

 

Curr Osteoporos Rep. 2008 Sep;6(3):95-9.

Evaluation and correction of low vitamin D status.

Binkley N, Krueger D.

University of Wisconsin Osteoporosis Research Program, 2870 University Avenue, Suite 100, Madison, WI 53705, USA. nbinkley@wisc.edu

Low vitamin D status, which is endemic due to inadequate oral intake combined with sun avoidance, contributes to musculoskeletal and other pathologies. Although controversial, it is increasingly recommended that serum 25-hydroxyvitamin D (25D) concentrations less than 30 ng/mL be considered suboptimal. Clinicians should appreciate that 25(OH)D measurements, like all quantitative laboratory tests, are subject to assay and biologic variability. Additionally, international standardized calibrators do not exist for 25(OH)D measurement. As such, a single 25(OH)D value of "30 ng/mL" may have substantial variability surrounding it, thereby making 25(OH)D levels of approximately 35 to 40 ng/mL a reasonable therapeutic goal to assure vitamin D adequacy. Achieving such levels often requires vitamin D supplementation. Vitamin D3 (cholecalciferol) or D2 (ergocalciferol) may be used; whether vitamin D3 is more potent than vitamin D2 in maintaining 25(OH)D is controversial.

 

 

HSS J. 2006 Sep;2(2):130-5.

How much calcium is in your drinking water? A survey of calcium concentrations in bottled and tap water and their significance for medical treatment and drug administration.

Morr S, Cuartas E, Alwattar B, Lane JM.

Hospital for Special Surgery, New York, NY, USA.

INTRODUCTION: Different forms of water vary in calcium content. High divalent ion (i.e., Ca(2+), Mg(2+), etc.) concentration is deleterious to the absorption and efficacy of the bisphosphonate group of drugs in osteoporosis treatment. Water with high calcium concentration may also present an alternate pathway of calcium administration. In either case, knowing the actual concentration is critical. HYPOTHESIS: The current paper is a surveillance study. We hypothesize that there is considerable variation in the calcium concentrations in the various water sources: tap water from US and Canadian cities of different regions and purified, spring, and mineral bottled waters. In addition, we hypothesize that the water filter removes a significant amount of minerals including calcium from the water. METHODOLOGY: Calcium concentrations in various city tap waters, as well as an assorted number of bottled waters, were determined through the direct inspection of scientific data. The effect of filtering was also determined by mineral analysis of mineral water directly before and after filtration. RESULT: The calcium concentration of water varies from 1 to 135 mg/L across the USA and Canada. Most spring waters were found to have a relatively low calcium concentration, with an average of 21.8 mg/L. Purified waters contain a negligible calcium concentration. Mineral waters, on the other hand, were generally found to contain higher calcium concentrations, an average of 208 mg/L of calcium. Filtration was found to remove a considerable amount of calcium from the water, removing 89% on average. CONCLUSION: Calcium concentration in water varied substantially from different sources in the USA and Canada. Bottled waters presented with concentrations of calcium covering a very large range. Certain tap and bottled waters present with concentrations of calcium sufficient to exhibit a deleterious effect on bisphosphonate treatment. Alternatively, certain waters may be used as a source of calcium that may provide over 40% of the recommended daily intake for calcium.

 

 

J Clin Endocrinol Metab. 2008 Aug 26. [Epub ahead of print]

Relations between endogenous androgens and estrogens in postmenopausal women with suspected ischemic heart disease.

Braunstein GD, Bairey Merz CN, Johnson BD, Stanczyk FZ, Bittner V, Berga SL, Shaw L, Hodgson TK, Paul-Labrador M, Azziz R.

Cedars-Sinai Medical Center, Los Angeles, CA; University of Pittsburgh, Pittsburgh, PA; University of Southern California, Los Angeles, CA; University of Alabama at Birmingham, Birmingham, AL; Emory University School of Medicine, Atlanta, GA.

Context: Since androgens are obligatory precursors of estrogens, it is reasonable to assume that their serum concentrations would exhibit positive correlations. If so, then epidemiologic studies that examine the association between androgens and pathologic processes should adjust the results for the independent effect of estrogens. Objective: To examine the interrelationships among testosterone (T), androstenedione (A), estradiol (E2), estrone (E1), and sex hormone-binding globulin (SHBG) in postmenopausal women. Design: Cross-sectional study of women participating in the NHBLI-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. Setting: Four academic medical centers. Patients: A total of 284 postmenopausal women with chest pain symptoms or suspected myocardial ischemia. Main Outcome Measures: Post-hoc analysis of the relationships among sex steroid hormones with insulin resistance, body mass index (BMI) and presence or absence of coronary artery disease as determined by coronary angiography. Results: BMI was significantly associated with insulin resistance, total E2, free E2, bioavailable E2, and free T. Highly significant correlations were found for total T, free T, and A with total E2, free E2, bioavailable E2 and E1, and persisted after adjustment for BMI and insulin resistance. A significant relationship was present between total and free T and the presence of coronary artery disease after adjustment for the effect of E2. Conclusions: Serum levels of androgens and estrogens track closely in postmenopausal women referred for coronary angiography for suspected myocardial ischemia. Epidemiologic studies that relate sex steroid hormones to physiological or pathological processes need to control for the independent effect of both estrogens and androgens.

 

 

J Cell Physiol. 2008 Aug 25. [Epub ahead of print]

Low dose beta-blocker prevents ovariectomy-induced bone loss in rats without affecting heart functions.

Bonnet N, Benhamou CL, Malaval L, Goncalves C, Vico L, Eder V, Pichon C, Courteix D.

INSERM U658, CTI (Caractérisation du tissu osseux par imagerie, techniques et applications), Université d'Orléans, Orleans, France.

Findings from animal studies have suggested that bone remodeling is under beta-adrenergic control. However, the level of adrenergic inhibition required to achieve the most favorable effects on the skeleton remains unknown. To address this question, we compared the effects of low (0.1 mg/Kg/day), medium (5 mg/Kg/day) or high (20 mg/Kg/day) doses of propranolol given 5 days per week for 10 weeks in ovariectomized (OVX) rats. Characteristics of bone microarchitecture, biomechanical properties and bone turnover were investigated, whilst heart functions were assessed by echocardiography and catheterization of the left ventricle. We first confirmed the expression of Adrbeta2R and the absence of Adrbeta1R on osteoblasts by PCR and confocal microscopy. We then showed that low dose propranolol prevented OVX induced bone loss by increasing bone formation (+30% of MAR vs. placebo, P = 0.01) and decreasing bone resorption (-52% of osteoclast surface on bone surface vs. placebo, P = 0.01). Consequently, rats receiving 0.1 mg/kg/day propranolol displayed higher stress (+27%), intrinsic energy (+28.7%) and Young's Modulus in compression versus placebo (all, P < 0.05). No significant effects on heart hemodynamic parameters were found in rats receiving this dose. In contrast, medium and high doses of propranolol had a negative effect on heart functions but no significant protective effects on bone mass in ovariectomized rats. These results, consistent with the dominant nature of the high bone mass phenotype and normal heart function of Adrbeta2R-deficient mice, suggest that low doses of beta-blockers may have a therapeutic utility in the treatment of osteoporosis with high selectivity for bone tissues.

 

 

Menopause. 2008 Aug 22. [Epub ahead of print]

Changes in skin topography during hormone therapy.

Kaatz M, Elsner P, Koehler MJ.

From the Department of Dermatology and Allergology, Friedrich Schiller University, Jena, Germany.

The influence of female sex hormones on skin aging has repeatedly been investigated with contradictory results. In our study, the skin roughness of eight women receiving hormone therapy decreased significantly by approximately 15% in 12 months. Our results provide new evidence of the antiaging effect of female sex hormones.

 

 

Menopause. 2008 Aug 22. [Epub ahead of print]

Newer antidepressants for hot flashes-should their efficacy still be up for debate?

Loprinzi CL, Barton DL, Sloan JA, Novotny PJ, Wolf S.

From the Departments of 1Oncology and 2Biostatistics, Mayo Clinic, Rochester, MN.

OBJECTIVE:: Newer antidepressants have been shown in clinical trials to reduce hot flashes, although not as well as do hormones. Nonetheless, a recently published meta-analysis and subsequent editorial raised doubts with regard to the utility of newer antidepressants for treating hot flashes. Concerns about the lack of efficacy of newer antidepressants on hot flashes were based in large part on results of two placebo-controlled, double-blind trials, one evaluating venlafaxine and the other individually evaluating both fluoxetine and citalopram. These two studies have repeatedly been put forward as evidence that newer antidepressants are not definitively proven to reduce hot flashes. DESIGN:: Raw data from these two randomized, placebo-controlled trials evaluating second-generation antidepressants for hot flashes were obtained. These data and subsequent study conclusions are evaluated and discussed in the context of other published trial data regarding the use of newer antidepressants for treating hot flashes. RESULTS:: Examination of the raw data from these two trials revealed that neither employed a baseline period of hot flash determination against which to calculate changes over time from baseline. CONCLUSIONS:: Recognition that these two trials cannot be used to look at hot flash frequency or score changes from baseline limits their ability to inform the efficacy literature about the use of newer antidepressants for hot flash reduction.

 

 

Selección de Resúmenes de Menopausia

Semana del 03 al 09 de Septiembre 2008

Juan Enrique Blümel. Departamento Medicina Sur. Universidad de Chile

 

 

 

 

 

Menopause. 2008 Aug 26. [Epub ahead of print]

Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy.

Rocca WA, Grossardt BR, Geda YE, Gostout BS, Bower JH, Maraganore DM, de Andrade M,

From the Divisions of 1Epidemiology and 2Biostatistics, Department of Health Sciences Research; Departments of 3Psychiatry and Psychology, 4Obstetrics and Gynecology, and 5Neurology, College of Medicine, Mayo Clinic, Rochester, MN.

OBJECTIVE:: We studied the long-term risk of depressive and anxiety symptoms in women who underwent bilateral oophorectomy before menopause. DESIGN:: We conducted a cohort study among all women residing in Olmsted County, MN, who underwent bilateral oophorectomy before the onset of menopause for a noncancer indication from 1950 through 1987. Each member of the bilateral oophorectomy cohort was matched by age with a referent woman from the same population who had not undergone an oophorectomy. In total, we studied 666 women with bilateral oophorectomy and 673 referent women. Women were followed for a median of 24 years, and depressive and anxiety symptoms were assessed using a structured questionnaire via a direct or proxy telephone interview performed from 2001 through 2006. RESULTS:: Women who underwent bilateral oophorectomy before the onset of menopause had an increased risk of depressive symptoms diagnosed by a physician (hazard ratio = 1.54, 95% CI: 1.04-2.26, adjusted for age, education, and type of interview) and of anxiety symptoms (adjusted hazard ratio = 2.29, 95% CI: 1.33-3.95) compared with referent women. The findings remained consistent after excluding depressive or anxiety symptoms that first occurred within 10 years after oophorectomy. The associations were greater with younger age at oophorectomy but did not vary across indications for the oophorectomy. In addition, treatment with estrogen to age 50 years in women who underwent bilateral oophorectomy at younger ages did not modify the risk. CONCLUSIONS:: Bilateral oophorectomy performed before the onset of menopause is associated with an increased long-term risk of depressive and anxiety symptoms.

 

 

Menopause. 2008 Aug 21. [Epub ahead of print]

Effect of progestogen and progestogen type on hemostasis measures in postmenopausal women: the Postmenopausal Estrogen/Progestin Intervention (PEPI) Study.

Smith NL, Wiley JR, Legault C, Rice KM, Heckbert SR, Psaty BM, Tracy RP, Cushman M.

From the Departments of 1Epidemiology, 2Medicine, 3Biostatistics, and 4Health Services, University of Washington, Seattle, WA; 5Seattle Epidemiologic Research and Information Center of the Department of Veterans Affairs Office of Research and Development, Seattle, WA; 6Department of Public Health Sciences, Wake Forest University, Winston-Salem, NC; and 7Departments of Pathology and Laboratory Medicine, University of Vermont, Burlington, VT.

OBJECTIVE:: The contribution of progestogen therapy or progestogen type to risks and benefits of estrogen treatment is inadequately characterized. We examined the effect of conjugated equine estrogens (CEE) with and without concomitant progestogen treatments on changes in hemostasis measures among Postmenopausal Estrogen/Progestin Intervention participants. DESIGN:: Postmenopausal Estrogen/Progestin Intervention was a clinical trial that randomized 875 postmenopausal women to one of five arms: placebo, CEE alone, CEE with cyclic micronized progesterone (MP), CEE with cyclic medroxyprogesterone acetate (MPA), and CEE with continuous MPA. Twelve hemostasis assays were measured in a substudy at baseline and 12 and 36 months. Using 12- and 36-month changes in hemostasis measures, we calculated change ratios for two comparisons of active treatments: CEE+MPA versus CEE and CEE+MPA versus CEE+MP. RESULTS:: Hemostasis measures were available for 288 women. Compared with women assigned to CEE alone, 12-month increases in factor VIIc and protein C among women assigned to CEE+MPA were relatively smaller (ratios: 0.94 [95% CI: 0.89-0.98] and 0.96 [95% CI: 0.92-1.00]), respectively. Compared with women assigned to CEE+MP, women assigned to CEE+MPA had smaller increases in factor VIIc and larger decreases in plasminogen activator inhibitor-1 antigen at 12 months (ratios: 0.94 [95% CI: 0.90-0.98] and 0.70 [95% CI: 0.53-0.93], respectively). Thirty-six month ratios were similar to these. Women assigned to CEE+MPA had smaller increases in protein C than those assigned CEE+MP at 36 months only (ratio: 0.95 [95% CI: 0.91-0.99]). No other associations were significant. CONCLUSIONS:: We found modest yet significant differences in hemostasis measure changes when comparing progestogen use and progestogen type in postmenopausal women using CEE.

 

 

Cancer Epidemiol Biomarkers Prev. 2008 Aug 25. [Epub ahead of print]

Estrogen plus Progestin and Risk of Benign Proliferative Breast Disease.

Rohan TE, Negassa A, Chlebowski RT, Lasser NL, McTiernan A, Schenken RS, Ginsberg M, Wassertheil-Smoller S, Page DL.

Albert Einstein College of Medicine, Bronx, New York; Harbor-UCLA Medical Center, Torrance, California; New Jersey Medical School, Newark, New Jersey; Fred Hutchinson Cancer Research Center, Seattle, Washington; University of Texas Health Science Center, San Antonio, Texas; and Vanderbilt University Medical School, Nashville, Tennessee.

Women with benign proliferative breast disease are at increased risk of subsequent breast cancer. Estrogens and progesterone exert proliferative effects on mammary epithelium, and combined hormone replacement therapy has been associated with increased breast cancer risk. We tested the effect of conjugated equine estrogen plus progestin on the risk of benign proliferative breast disease in the Women's Health Initiative (WHI) randomized controlled trial. In the WHI trial of estrogen plus progestin, 16,608 postmenopausal women were randomly assigned either to 0.625 mg/day of conjugated equine estrogen plus 2.5 mg/day of medroxyprogesterone acetate or to placebo. Baseline and annual breast exams and mammograms were required. The trial was terminated early (average follow-up, 5.5 years). We identified women who had had a biopsy for benign breast disease, and subjected histologic sections from the biopsies to standardized review. Overall, 178 incident cases of benign proliferative breast disease were ascertained in the estrogen plus progestin group and 99 in the placebo group. The use of estrogen plus progestin was associated with a 74% increase in the risk of benign proliferative breast disease [hazard ratio, 1.74; 95% confidence interval (CI), 1.35-2.25]. For benign proliferative breast disease without atypia the hazard ratio was 2.00 (95% CI, 1.50-2.66), while for atypical hyperplasia it was 0.76 (95% CI, 0.38-1.52). The risk varied little by levels of baseline characteristics. The results of this study suggest that the use of estrogen plus progestin may increase the risk of benign proliferative breast disease.

 

 

Curr Osteoporos Rep. 2008 Sep;6(3):95-9.

Evaluation and correction of low vitamin D status.

Binkley N, Krueger D.

University of Wisconsin Osteoporosis Research Program, 2870 University Avenue, Suite 100, Madison, WI 53705, USA. nbinkley@wisc.edu

Low vitamin D status, which is endemic due to inadequate oral intake combined with sun avoidance, contributes to musculoskeletal and other pathologies. Although controversial, it is increasingly recommended that serum 25-hydroxyvitamin D (25D) concentrations less than 30 ng/mL be considered suboptimal. Clinicians should appreciate that 25(OH)D measurements, like all quantitative laboratory tests, are subject to assay and biologic variability. Additionally, international standardized calibrators do not exist for 25(OH)D measurement. As such, a single 25(OH)D value of "30 ng/mL" may have substantial variability surrounding it, thereby making 25(OH)D levels of approximately 35 to 40 ng/mL a reasonable therapeutic goal to assure vitamin D adequacy. Achieving such levels often requires vitamin D supplementation. Vitamin D3 (cholecalciferol) or D2 (ergocalciferol) may be used; whether vitamin D3 is more potent than vitamin D2 in maintaining 25(OH)D is controversial.

 

 

HSS J. 2006 Sep;2(2):130-5.

How much calcium is in your drinking water? A survey of calcium concentrations in bottled and tap water and their significance for medical treatment and drug administration.

Morr S, Cuartas E, Alwattar B, Lane JM.

Hospital for Special Surgery, New York, NY, USA.

INTRODUCTION: Different forms of water vary in calcium content. High divalent ion (i.e., Ca(2+), Mg(2+), etc.) concentration is deleterious to the absorption and efficacy of the bisphosphonate group of drugs in osteoporosis treatment. Water with high calcium concentration may also present an alternate pathway of calcium administration. In either case, knowing the actual concentration is critical. HYPOTHESIS: The current paper is a surveillance study. We hypothesize that there is considerable variation in the calcium concentrations in the various water sources: tap water from US and Canadian cities of different regions and purified, spring, and mineral bottled waters. In addition, we hypothesize that the water filter removes a significant amount of minerals including calcium from the water. METHODOLOGY: Calcium concentrations in various city tap waters, as well as an assorted number of bottled waters, were determined through the direct inspection of scientific data. The effect of filtering was also determined by mineral analysis of mineral water directly before and after filtration. RESULT: The calcium concentration of water varies from 1 to 135 mg/L across the USA and Canada. Most spring waters were found to have a relatively low calcium concentration, with an average of 21.8 mg/L. Purified waters contain a negligible calcium concentration. Mineral waters, on the other hand, were generally found to contain higher calcium concentrations, an average of 208 mg/L of calcium. Filtration was found to remove a considerable amount of calcium from the water, removing 89% on average. CONCLUSION: Calcium concentration in water varied substantially from different sources in the USA and Canada. Bottled waters presented with concentrations of calcium covering a very large range. Certain tap and bottled waters present with concentrations of calcium sufficient to exhibit a deleterious effect on bisphosphonate treatment. Alternatively, certain waters may be used as a source of calcium that may provide over 40% of the recommended daily intake for calcium.

 

 

J Clin Endocrinol Metab. 2008 Aug 26. [Epub ahead of print]

Relations between endogenous androgens and estrogens in postmenopausal women with suspected ischemic heart disease.

Braunstein GD, Bairey Merz CN, Johnson BD, Stanczyk FZ, Bittner V, Berga SL, Shaw L, Hodgson TK, Paul-Labrador M, Azziz R.

Cedars-Sinai Medical Center, Los Angeles, CA; University of Pittsburgh, Pittsburgh, PA; University of Southern California, Los Angeles, CA; University of Alabama at Birmingham, Birmingham, AL; Emory University School of Medicine, Atlanta, GA.

Context: Since androgens are obligatory precursors of estrogens, it is reasonable to assume that their serum concentrations would exhibit positive correlations. If so, then epidemiologic studies that examine the association between androgens and pathologic processes should adjust the results for the independent effect of estrogens. Objective: To examine the interrelationships among testosterone (T), androstenedione (A), estradiol (E2), estrone (E1), and sex hormone-binding globulin (SHBG) in postmenopausal women. Design: Cross-sectional study of women participating in the NHBLI-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. Setting: Four academic medical centers. Patients: A total of 284 postmenopausal women with chest pain symptoms or suspected myocardial ischemia. Main Outcome Measures: Post-hoc analysis of the relationships among sex steroid hormones with insulin resistance, body mass index (BMI) and presence or absence of coronary artery disease as determined by coronary angiography. Results: BMI was significantly associated with insulin resistance, total E2, free E2, bioavailable E2, and free T. Highly significant correlations were found for total T, free T, and A with total E2, free E2, bioavailable E2 and E1, and persisted after adjustment for BMI and insulin resistance. A significant relationship was present between total and free T and the presence of coronary artery disease after adjustment for the effect of E2. Conclusions: Serum levels of androgens and estrogens track closely in postmenopausal women referred for coronary angiography for suspected myocardial ischemia. Epidemiologic studies that relate sex steroid hormones to physiological or pathological processes need to control for the independent effect of both estrogens and androgens.

 

 

J Cell Physiol. 2008 Aug 25. [Epub ahead of print]

Low dose beta-blocker prevents ovariectomy-induced bone loss in rats without affecting heart functions.

Bonnet N, Benhamou CL, Malaval L, Goncalves C, Vico L, Eder V, Pichon C, Courteix D.

INSERM U658, CTI (Caractérisation du tissu osseux par imagerie, techniques et applications), Université d'Orléans, Orleans, France.

Findings from animal studies have suggested that bone remodeling is under beta-adrenergic control. However, the level of adrenergic inhibition required to achieve the most favorable effects on the skeleton remains unknown. To address this question, we compared the effects of low (0.1 mg/Kg/day), medium (5 mg/Kg/day) or high (20 mg/Kg/day) doses of propranolol given 5 days per week for 10 weeks in ovariectomized (OVX) rats. Characteristics of bone microarchitecture, biomechanical properties and bone turnover were investigated, whilst heart functions were assessed by echocardiography and catheterization of the left ventricle. We first confirmed the expression of Adrbeta2R and the absence of Adrbeta1R on osteoblasts by PCR and confocal microscopy. We then showed that low dose propranolol prevented OVX induced bone loss by increasing bone formation (+30% of MAR vs. placebo, P = 0.01) and decreasing bone resorption (-52% of osteoclast surface on bone surface vs. placebo, P = 0.01). Consequently, rats receiving 0.1 mg/kg/day propranolol displayed higher stress (+27%), intrinsic energy (+28.7%) and Young's Modulus in compression versus placebo (all, P < 0.05). No significant effects on heart hemodynamic parameters were found in rats receiving this dose. In contrast, medium and high doses of propranolol had a negative effect on heart functions but no significant protective effects on bone mass in ovariectomized rats. These results, consistent with the dominant nature of the high bone mass phenotype and normal heart function of Adrbeta2R-deficient mice, suggest that low doses of beta-blockers may have a therapeutic utility in the treatment of osteoporosis with high selectivity for bone tissues.

 

 

Menopause. 2008 Aug 22. [Epub ahead of print]

Changes in skin topography during hormone therapy.

Kaatz M, Elsner P, Koehler MJ.

From the Department of Dermatology and Allergology, Friedrich Schiller University, Jena, Germany.

The influence of female sex hormones on skin aging has repeatedly been investigated with contradictory results. In our study, the skin roughness of eight women receiving hormone therapy decreased significantly by approximately 15% in 12 months. Our results provide new evidence of the antiaging effect of female sex hormones.

 

 

Menopause. 2008 Aug 22. [Epub ahead of print]

Newer antidepressants for hot flashes-should their efficacy still be up for debate?

Loprinzi CL, Barton DL, Sloan JA, Novotny PJ, Wolf S.

From the Departments of 1Oncology and 2Biostatistics, Mayo Clinic, Rochester, MN.

OBJECTIVE:: Newer antidepressants have been shown in clinical trials to reduce hot flashes, although not as well as do hormones. Nonetheless, a recently published meta-analysis and subsequent editorial raised doubts with regard to the utility of newer antidepressants for treating hot flashes. Concerns about the lack of efficacy of newer antidepressants on hot flashes were based in large part on results of two placebo-controlled, double-blind trials, one evaluating venlafaxine and the other individually evaluating both fluoxetine and citalopram. These two studies have repeatedly been put forward as evidence that newer antidepressants are not definitively proven to reduce hot flashes. DESIGN:: Raw data from these two randomized, placebo-controlled trials evaluating second-generation antidepressants for hot flashes were obtained. These data and subsequent study conclusions are evaluated and discussed in the context of other published trial data regarding the use of newer antidepressants for treating hot flashes. RESULTS:: Examination of the raw data from these two trials revealed that neither employed a baseline period of hot flash determination against which to calculate changes over time from baseline. CONCLUSIONS:: Recognition that these two trials cannot be used to look at hot flash frequency or score changes from baseline limits their ability to inform the efficacy literature about the use of newer antidepressants for hot flash reduction.

 

 

 

Selección de Resúmenes de Menopausia

Semana del 10 al 16 de Septiembre 2008

Juan Enrique Blümel. Departamento Medicina Sur. Universidad de Chile

 

 

 

 

 

Menopause. 2008 Sep 4. [Epub ahead of print]

A proposed classification system for menstrual cycles in the menopause transition based on changes in serum hormone profiles.

Robertson DM, Hale GE, Fraser IS, Hughes CL, Burger HG.

From the 1Prince Henry's Institute, Monash Medical Centre, Clayton, Victoria, Australia; 2Department of Obstetrics and Gynaecology, University of Sydney, NSW, Australia; and 3Quintiles Inc., Research Triangle Park, NC.

OBJECTIVE:: To characterize menstrual cycles in women in late reproductive age and the menopause transition, based on changes in serum hormone levels. DESIGN:: Serum levels of estradiol, progesterone, follicle-stimulating hormone (FSH), luteinizing hormone, inhibin A, inhibin B, and antimüllerian hormone, as previously reported as mean data grouped according to the Stages of Reproductive Aging Workshop proposals, were analyzed in 55 women aged 45 to 55 and compared with those in 21 women aged 21 to 35. RESULTS:: The ovulatory cycles in the older women were divided into three types. Type 1 cycles (n = 14, 33%) were those with hormone concentrations similar to the women aged 21 to 35 except for 20-fold lower antimüllerian hormone levels. Type 2 cycles (n = 24; 53%) had increased FSH, decreased inhibin B, and increased FSH-to-inhibin B ratios but normal estradiol and progesterone levels. Type 3 cycles had the same characteristics as type 2 cycles (n = 5; 12%) in addition to lower luteal phase progesterone and increased luteinizing hormone. CONCLUSIONS:: The changes in hormone levels indicated in cycle types 1 to 3 closely reflect the changes in ovarian-pituitary activity as menopause approaches and are likely to be directly attributable to a decrease in ovarian follicle reserve. The findings suggest that FSH-to-inhibin B ratios and antimüllerian hormone are distinct early indicators of the menopause transition and are likely to be useful biomarkers of impending menopause. Furthermore, this classification may provide an improved basis for the study of reproductive endocrine disorders associated with the menopause transition.

 

 

Maturitas. 2008 Sep 3. [Epub ahead of print]

Effects of estradiol on the cognitive function of postmenopausal women.

Marinho RM, Soares JM Jr, Santiago RC, Maganhin CC, Machado F, de Miranda Cota AM, Baracat EC.

Federal University of Sâo Paulo and Faculdade de Ciências Médicas de Minas Gerais, Brazil.

OBJECTIVE: To analyze the effect of estrogen on the cognitive function of postmenopausal women through psychometric tests. METHODS: Seventy-four postmenopausal women were divided into two groups: (G1) estrogen group (n=34), treated with 2mg 17 beta-estradiol; (G2) placebo group (n=31), treated with inactive substance. All the participants were submitted, before and after treatment, to psychometric tests, Greene's Scale of Climacteric Symptoms and the Hamilton Scale for depression. Statistical analysis was performed using the Mann-Whitney test and Student's t-test. In order to evaluate the degree of improvement of symptoms or depression after estrogen treatment, Spearman's correlation coefficient was calculated. RESULTS: A few psychometric tests (immediate and late recall of story, Trailmaking A and B, FAS, Stroop, Bells tests) showed post-intervention improvement, but these were not significant when compared to the placebo group's data. The estrogen group's climacteric symptoms were mitigated in comparison to placebo's, but there was no significant difference between the two groups on the Hamilton Scale. Reduction in climacteric symptoms was associated with improvement in executive function performance as evaluated by the Stroop test. CONCLUSION: Our results suggest estrogen improves the cognitive function, possibly due to a decrease in vasomotor symptoms.

 

 

Maturitas. 2008 Sep 4. [Epub ahead of print]

Could transdermal estradiol + progesterone be a safer postmenopausal HRT? A review.

L'hermite M, Simoncini T, Fuller S, Genazzani AR.

Department of Gynecology and Obstetrics, Université Libre de Bruxelles, Bruxelles, Belgium.

Hormone replacement therapy (HRT) in young postmenopausal women is a safe and effective tool to counteract climacteric symptoms and to prevent long-term degenerative diseases, such as osteoporotic fractures, cardiovascular disease, diabetes mellitus and possibly cognitive impairment. The different types of HRT offer to many extent comparable efficacies on symptoms control; however, the expert selection of specific compounds, doses or routes of administration can provide significant clinical advantages. This paper reviews the role of the non-oral route of administration of sex steroids in the clinical management of postmenopausal women. Non-orally administered estrogens, minimizing the hepatic induction of clotting factors and others proteins associated with the first-pass effect, are associated with potential advantages on the cardiovascular system. In particular, the risk of developing deep vein thrombosis or pulmonary thromboembolism is negligible in comparison to that associated with oral estrogens. In addition, recent indications suggest potential advantages for blood pressure control with non-oral estrogens. To the same extent, a growing literature suggests that the progestins used in association with estrogens may not be equivalent. Recent evidence indeed shows that natural progesterone displays a favorable action on the vessels and on the brain, while this might not be true for some synthetic progestins. Compelling indications also exist that differences might also be present for the risk of developing breast cancer, with recent trials indicating that the association of natural progesterone with estrogens confers less or even no risk of breast cancer as opposed to the use of other synthetic progestins. In conclusion, while all types of hormone replacement therapies are safe and effective and confer significant benefits in the long-term when initiated in young postmenopausal women, in specific clinical settings the choice of the transdermal route of administration of estrogens and the use of natural progesterone might offer significant benefits and added safety.

 

 

J Endocrinol Invest. 2008 Jul;31(7):597-601.

Sex hormone binding globulin levels across the adult lifespan in women - The role of body mass index and fasting insulin.

Maggio M, Lauretani F, Basaria S, Ceda GP, Bandinelli S, Metter EJ, Bos AJ, Ruggiero C, et al. Internal Medicine and Biomedical Sciences, Section of Geriatrics, University of Parma, Parma, Italy.

SHBG is a major carrier of androgens. In men, SHBG levels increase with age, while in women data are scant. There is evidence that body mass index (BMI) and fasting insulin influence SHBG concentration. Since low SHBG levels are predictors of insulin resistance and diabetes, understanding the relationship of SHBG with age, insulin, and BMI is important to gain insight into the role of SHBG as a cardiovascular risk factor in women. Differences in SHBG across adult life span and their relationship with insulin and BMI were evaluated in a representative cohort of 616 Italian women free of diabetes and not on hormone replacement therapy enrolled in the InCHIANTI Study. The relationship of SHBG with age, BMI, and fasting insulin levels was analyzed using linear regression and by loess smoother. Serum SHBG levels showed a U-shaped trajectory with age, declining from the 2nd to the 6th decade of life and increasing after the 6th decade (p<0.0001). Age-related trends for BMI and fasting insulin mirrored the trend observed for SHBG. After adjusting for fasting insulin, the relationship between log (SHBG) and age square was attenuated (beta coefficient from 0.00044 to 0.00039) and was further reduced after adjustment for BMI (from 0.00039 to 0.00028). SHBG levels show an age-related U-shaped trajectory. These changes mirror the age-related changes in BMI and fasting insulin, suggesting that BMI and insulin negatively influence SHBG concentration.

 

 

Neuroepidemiology. 2008 Sep 11;31(3):167-173. [Epub ahead of print]

Functional Decline in Cognitive Impairment - The Relationship between Physical and Cognitive Function.

Auyeung TW, Kwok T, Lee J, Leung PC, Leung J, Woo J.

Jockey Club Center for Osteoporosis Care and Control, Hong Kong, SAR, China.

Background: Physical function decline is associated with dementia, which might either be mediated by the coexisting sarcopenia or directly related to the impaired cognition. Our objectives are to examine the relationship between cognitive function and performance-based physical function and to test the hypothesis that cognitive function is related to poor physical function independent of muscle mass. Methods: We measured muscle strength, performance-based physical function and muscle mass using dual-energy X-ray absorptiometry and cognitive function using the cognitive part of the Community Screening Instrument of Dementia (CSI-D) in 4,000 community-dwelling Chinese elderly aged >65 years. A CSI-D cognitive score of >28.40 was considered as cognitively impaired. The effect of cognitive impairment on muscle strength and physical function was analyzed by multivariate analysis with adjustment for age, appendicular skeletal mass (ASM), the Physical Activity Scale for the Elderly (PASE) and other comorbidities. Results: In both genders, the cognitively impaired (CSI-D cognitive score >28.40) group had a weaker grip strength (-5.10 kg, p < 0.001 in men; -1.08 kg in women, p < 0.001) and performed worse in the two physical function tests (in men, 6-meter walk speed, -0.13 m/s, p < 0.001, chair stand test, 1.42 s, p < 0.001; in women, 6-meter walk speed, -0.08 m/s, p < 0.001, chair stand test, 1.48 s, p < 0.001). After adjustment for age, ASM, PASE and other comorbidities, significant differences in grip strength (-2.60 kg, p < 0.001 in men; -0.49 kg, p = 0.011 in women) and the two physical function tests persisted between the cognitively impaired and nonimpaired group (in men, 6-meter walk speed, -0.072 m/s, p < 0.001, chair stand test, 0.80 s, p = 0.045; in women, 6-meter walk speed, -0.049 m/s, p < 0.001, chair stand test, 0.98 s, p < 0.001). Conclusions: Poor physical function and muscle strength coexisted with cognitive impairment. This relationship was independent of muscle mass. It is likely therefore that the functional decline in dementia might be related directly to factors resulting in cognitive impairment independently of the coexisting sarcopenia.

 

 

Curr Diab Rep. 2008 Oct;8(5):393-8.

Diabetes and the vitamin D connection.

Holick MF.

Department of Medicine, Section of Endocrinology, Nutrition, and Diabetes, Boston University School of Medicine, 715 Albany Street, M-1013, Boston, MA 02118, USA. mfholick@bu.edu

Vitamin D deficiency, which is common in children and adults, causes rickets, osteomalacia, and osteoporosis. Most organs and immune cells have a vitamin D receptor, and some also have the capacity to metabolize 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D. 1,25-Dihydroxyvitamin D is a potent immunomodulator that also enhances the production and secretion of several hormones, including insulin. Vitamin D deficiency has been associated with increased risk of type 1 diabetes. Glycemic control and insulin resistance are improved when vitamin D deficiency is corrected and calcium supplementation is adequate. 25-Hydroxyvitamin D (measure of vitamin D status) of less than 20 ng/mL is vitamin D deficiency and 21 to 29 ng/mL is insufficiency. Children and adults need at least 1000 IU of vitamin D per day to prevent deficiency when there is inadequate sun exposure.

 

 

Climacteric. 2008 Oct;11(5):422-8.

Restless legs syndrome among women: prevalence, co-morbidity and possible relationship to menopause.

Wesstrom J, Nilsson S, Sundstrom-Poromaa I, Ulfberg J.

Department of Women's and Children's Health, Uppsala University.

Objectives Restless legs syndrome (RLS) is a common neurological movement disorder with a female preponderance and an increasing prevalence with age. During the menopausal transition, sleep is affected. Prior studies suggest that female hormones are associated with the clinical manifestation of RLS. Methods A random sample of 5000 women aged 18-64 years was selected from the general Swedish population. They were sent questions on RLS, general health, sleep problems, reproductive health and menopausal state. Results The response rate was 70.3%; 15.7% of the women were diagnosed with RLS. Prevalence increased with age. RLS subjects more often had symptoms of affected sleep and depressed mood. Co-morbidity with heart disease was more common among RLS subjects, whereas hypertension and diabetes mellitus were not. There was a strong association between vasomotor symptoms and RLS but no statistical relationship between use of hormone replacement therapy, postmenopausal state and RLS. Conclusion The prevalence of RLS among Swedish women is high. RLS sufferers more often suffered from depression and heart disease, whereas no such associations were noted for diabetes or hypertension. We found an increased prevalence of RLS among women with vasomotor symptoms (night sweats) during the m

 

 

Climacteric. 2008 Oct;11(5):416-21.

Characteristics of external genitalia in pre- and postmenopausal women.

Basaran M, Kosif R, Bayar U, Civelek B.

Department of Obstetrics and Gynecology.

Objective To determine those objective measurements that characterize the differences between the external genital organs of pre- and postmenopausal women. Methods During the study period, 50 premenopausal and 50 postmenopausal patients were recruited. Only women who were admitted for routine control examinations were consecutively included in the study. Exclusion criteria were previous history of pelvic surgery including external and internal genital organs, presence of diseases that may change the anatomy of external genital organs, Mullerian anomalies, previous vaginal birth with mediolateral episiotomy, and use of hormone replacement therapy. The following measurements were performed: length and width of clitoris, labium majus, and labium minus, the distance between the clitoris and urethra, perineal length, and length of vagina. Results The length of the vagina and the width of the labium minus were significantly different between the two groups. Mean vaginal length was significantly longer in premenopausal women compared to postmenopausal women (90.3 +/- 14.8 mm vs. 82.3 +/- 11.2 mm, respectively). The labia minora were wider in premenopausal women than in postmenopausal women (17.9 +/- 4.1 mm vs. 15.4 +/- 4.7 mm). Conclusions Characterization of the anatomical changes and relationships of external genitalia in postmenopausal women is important for functional and perioperative evaluation. In addition to reconstructive surgical procedures, determination of the objective measurements of anatomical landmarks in postmenopausal external genitalia might also be useful for assessing the results of treatment of 'atrophic' changes in women.

 

 

Climacteric. 2008 Oct;11(5):383-9.

Relation between body mass index and endothelium-dependent vasodilatation in healthy postmenopausal women.

Cagnacci A, Cannoletta M, Arangino S, Generali M, Ferrari S, Volpe A.

Department of Obstetrics, Gynecology and Pediatrics, Gynecology Unit, Policlinico of Modena, Modena.

Objective To evaluate whether endothelium-dependent vasodilatation is related to anthropometric parameters in 105 healthy postmenopausal women 47-68 years of age. Methods Flow-dependent, endothelium-dependent vasodilatation was considered as the maximal dilatation following deflation of a cuff placed on the forearm and inflated to supra-systolic blood pressure values for 4 min. Endothelium-independent vasodilatation was considered as the maximal dilatation induced by sublingual nitroglycerine (400 mug). Results Among parameters such as height, weight, body mass index (BMI), waist, hip, waist/hip ratio, lipids, glucose or insulin, only BMI, an indirect index of adiposity, was independently and directly related to baseline brachial artery diameter (b = 0.042, r = 0.269, p = 0.0055) and flow-mediated endothelium-dependent vasodilatation either expressed as net (b = 0.034, r = 0.315, p = 0.001) or percentage (b = 0.376, r = 0.202, p = 0.039) change. Stratification for BMI categories showed that women with BMI < 22 kg/m(2) had an endothelium-dependent vasodilatation, significantly lower than that of women with BMI >/= 30 kg/m(2) (0.711 +/- 0.076 mm vs. 1.107 +/- 0.141 mm; p = 0.0114). BMI was not related to endothelium-independent vasodilatation. Conclusions Present results show that, in healthy postmenopausal women, endothelium-dependent vasodilatation is related to BMI, arteries of slender women dilating less than those of their heavier counterparts. A low BMI does not appear to be beneficial for artery vasodilatation in healthy postmenopausal women.

 

 

Climacteric. 2008 Oct;11(5):355-63.

Oral contraceptives, hormone therapy and cardiovascular risk.

Shapiro S.

Emeritus Professor of Epidemiology, Boston University, USA.

Background Soon after combined estrogen/progestogen oral contraceptives (COCs) were introduced in the 1950s, it was established that they cause venous thromboembolism (VTE), that the risk is related to estrogen dose, and that COCs also increase the risk of myocardial infarction among female smokers over age 35. Stroke risk is also increased. Early studies of supplemental hormone therapy were inconclusive. Objective To consider new findings. New findings on oral contraceptives Genetic predisposition to VTE has been established with the discovery of Leiden factor V mutation. Based on an irrational classification of low-estrogen-dose (</= 30 mug ethinylestradiol) COCs as 'second generation' (containing 'older' progestogens, mainly norethisterone), or 'third generation' (containing the 'newer' progestogens, desogestrel or gestodene), it was claimed that the latter cause more VTE than the former. That claim has been rebutted, and it has been shown that VTE is a class effect, also shared by the newest progestogen, drosperinone. VTE risk is now known to be greatest during the initial year of COC use, after which the risk remains elevated, but somewhat less so. New findings on hormone therapy It is now established that hormone therapy increases the risk of VTE, and perhaps of stroke. The pattern is much the same as for oral contraceptives. Based on data from the Women's Health Initiative (WHI), a purportedly controlled trial, it was first claimed that estrogen plus progestogen therapy increases the overall risk of myocardial infarction. Then that claim was modified to suggest that therapy increases the risk mainly during the first year, and that the overall risk may possibly be reduced among recently menopausal women. Recently, based on the WHI data, and on data from an observational follow-up component of the WHI, the risks of myocardial infarction, VTE and stroke appeared to be increased maximally after therapy commenced, and then to decline to levels of little or no increased risk. Conclusions It is likely that the WHI studies were biased and that they overestimated the overall and time- and duration-specific risks of VTE, myocardial infarction and stroke. Particularly for myocardial infarction, a protective effect, perhaps strongest among the youngest women, but present at all ages, may correctly have been identified in earlier observational studies, and have been missed in the WHI studies.

 

 

Menopause. 2008 Sep 4. [Epub ahead of print]

Prevalence of symptoms in relation to androgen concentrations in women using estrogen plus progestogen and women using estrogen alone.

Spetz AC, Fredriksson MG, Lidfeldt J, Samsioe GN.

Department of Clinical Sciences, Lund University, Lund, Sweden.

OBJECTIVE:: Women using estrogen plus progestogen therapy sometimes report difficult to describe symptoms, eg, changes in libido, mood, and memory, that may be related to decreased androgens. To evaluate the prevalence of such symptoms and relate these symptoms to androgen levels in women using estrogen plus progestogen therapy, data from the Women's Health in the Lund Area Study were analyzed. DESIGN:: A total of 2,816 women using estrogen plus progestogen therapy were asked to complete a questionnaire consisting of questions concerning sexual well-being and different aspects of quality of life. Serum concentrations of testosterone, androstendione, sex hormone-binding globulin, and estradiol were measured. RESULTS:: A total of 2,048 questionnaires were eligible for evaluation. Almost 40% of the women reported decreased libido. Approximately 70% were satisfied with their current sex life. Eight percent reported that intercourse was unpleasant because of vaginal dryness. No evident associations were found between libido and serum hormone concentrations. The most positive effects of estrogen plus progestogen therapy concerning memory and urinary tract and vaginal complaints were found in women with the highest and/or moderate testosterone levels (P < 0.05). CONCLUSIONS:: We found no strong association between symptoms related to sexual well-being or quality of life and androgen concentrations in this study. Estrogen plus progestogen therapy did not seem to affect symptoms that might be related to low levels of androgens in the group of climacteric women whom we studied.

 

 

Menopause. 2008 Sep-Oct;15(5):958-62.

The relationship of self-reported sleep disturbance, mood, and menopause in a community study.

Cheng MH, Hsu CY, Wang SJ, Lee SJ, Wang PH, Fuh JL.

Department of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, Taiwan.

OBJECTIVE: The aim of this study was to assess the relationship between sleep disturbance, mood, menopausal status, and vasomotor symptoms in middle-aged women in Kinmen. DESIGN: A community-based sample of 1,113 Taiwanese women aged 43 to 57 years who were living on the island of Kinmen were recruited in this cross-sectional study. Menopausal status was determined by menstrual history. Sleep quality was measured by self-reported sleep problems. Anxiety and depression were assessed by the Hospital Anxiety Depression Scale. RESULTS: Forty-six percent of middle-aged women reported feeling dissatisfied with their sleep. Total sleep hours were not significantly different as a function of menopausal status. Generally, the occurrence of sleep problems or poor sleep quality was most prevalent in the postmenopausal group and least prevalent in premenopausal women. After analysis by multiple logistic regression, menopausal status was the independent factor of difficulty initiating sleep and sleep fragmentation. The Hospital Anxiety Depression Scale anxiety score was related to all sleep problems except for "excessive daytime sleepiness" and "awakening without further sleep." CONCLUSIONS: Almost half of the Taiwanese middle-aged women felt dissatisfied with their sleep. Both menopausal status and higher anxiety score were associated with poor sleep quality of midlife women.

 

 

 

Selección de Resúmenes de Menopausia

Semana del 17 al 23 de Septiembre 2008

Juan Enrique Blümel. Departamento Medicina Sur. Universidad de Chile

 

 

 

 

 

Ann Intern Med. 2008 Sep 16;149(6):404-15.

Pharmacologic treatment of low bone density or osteoporosis to prevent fractures: a clinical practice guideline from the American College of Physicians.

Qaseem A, Snow V, Shekelle P, Hopkins R Jr, Forciea MA, Owens DK; Clinical Efficacy Assessment Subcommittee of the American College of Physicians.

American College of Physicians, Philadelphia, Pennsylvania 19106, USA. aqaseem@acponline.org

DESCRIPTION: The American College of Physicians (ACP) developed this guideline to present the available evidence on various pharmacologic treatments to prevent fractures in men and women with low bone density or osteoporosis. METHODS: Published literature on this topic was identified by using MEDLINE (1966 to December 2006), the ACP Journal Club database, the Cochrane Central Register of Controlled Trials (no date limits), the Cochrane Database of Systematic Reviews (no date limits), Web sites of the United Kingdom National Institute of Health and Clinical Excellence (no date limits), and the United Kingdom Health Technology Assessment Program (January 1998 to December 2006). Searches were limited to English-language publications and human studies. Keywords for search included terms for osteoporosis, osteopenia, low bone density, and the drugs listed in the key questions. This guideline grades the evidence and recommendations according to the ACP's clinical practice guidelines grading system. RECOMMENDATION 1: ACP recommends that clinicians offer pharmacologic treatment to men and women who have known osteoporosis and to those who have experienced fragility fractures (Grade: strong recommendation; high-quality evidence). RECOMMENDATION 2: ACP recommends that clinicians consider pharmacologic treatment for men and women who are at risk for developing osteoporosis (Grade: weak recommendation; moderate-quality evidence). RECOMMENDATION 3: ACP recommends that clinicians choose among pharmacologic treatment options for osteoporosis in men and women on the basis of an assessment of risk and benefits in individual patients (Grade: strong recommendation; moderate-quality evidence). RECOMMENDATION 4: ACP recommends further research to evaluate treatment of osteoporosis in men and women.

 

 

J Agric Food Chem. 2008 Sep 19. [Epub ahead of print]

Major Phenolic Compounds in Olive Oil Modulate Bone Loss in an Ovariectomy/Inflammation Experimental Model.

Puel C, Mardon J, Agalias A, Davicco MJ, Lebecque P, Mazur A, Horcajada MN, et al

This study was conducted to determine whether the daily consumption for 84 days of tyrosol and hydroxytyrosol, the main olive oil phenolic compounds, and olive oil mill wastewater (OMWW), a byproduct of olive oil production, rich in micronutrients, may improve bone loss in ovariectomized rats (an experimental model of postmenopausal osteoporosis) and in ovariectomized rats with granulomatosis inflammation (a model set up for senile osteoporosis). As expected, an induced chronic inflammation provoked further bone loss at total, metaphyseal, and diaphyseal sites in ovariectomized rats. Tyrosol and hydroxytyrosol prevented this osteopenia by increasing bone formation ( p < 0.05), probably because of their antioxidant properties. The two doses of OMWW extracts had the same protective effect on bone ( p < 0.05), whereas OMWW did not reverse established osteopenia. In conclusion, polyphenol consumption seems to be an interesting way to prevent bone loss.

 

 

Menopause. 2008 Sep 10. [Epub ahead of print]

The influence of physiological and surgical menopause on coronary heart disease risk markers.

Verhoeven MO, van der Mooren MJ, Teerlink T, Verheijen RH, Scheffer PG, Kenemans P.

From the Project "Aging Women",  the Netherlands.

OBJECTIVE:: To investigate the influence of physiological and surgical menopause on serum concentrations of coronary heart disease (CHD) risk markers and sex hormones. DESIGN:: Physiological menopausal transition was investigated in two studies. In a longitudinal study, 16 women were followed from 2 years before until 2 years after physiological menopause. In a case-control study, 27 early postmenopausal women were compared with 27 age-matched late premenopausal women. Surgical menopause was investigated in 11 women undergoing a prophylactic bilateral salpingo-oophorectomy. The following parameters were measured: serum concentrations of estradiol, follicle-stimulating hormone, inhibin A, inhibin B, asymmetric dimethylarginine, lipids, leptin, homocysteine, C-reactive protein, and coenzyme Q10, as well as weight and body mass index. RESULTS:: After physiological and surgical menopause, serum estradiol and inhibin A and B decreased, whereas follicle-stimulating hormone increased (all P values < 0.01). Serum asymmetric dimethylarginine, total and low-density lipoprotein cholesterol, and leptin concentrations were significantly higher in postmenopausal women compared with premenopausal women (all P values < 0.05). Serum homocysteine concentrations increased significantly during the physiological menopausal transition. Total and low-density lipoprotein cholesterol increased after surgical menopause (both P values = 0.01). None of the other parameters studied were influenced significantly by the menopausal transition. No difference in change in the various CHD risk markers investigated was observed between physiological and surgical menopause. CONCLUSIONS:: The CHD risk profile was affected unfavorably by both physiological and surgical menopause. Changes in most CHD risk markers were small, despite the substantial changes in hormonal parameters.

 

 

Osteoporos Int. 2008 Sep 19. [Epub ahead of print]

The impact of incident fractures on health-related quality of life: 5 years of data from the Canadian Multicentre Osteoporosis Study.

Papaioannou A, Kennedy CC, Ioannidis G, Sawka A, Hopman WM, Pickard L, Brown JP, et al.

McMaster University, Hamilton Health Sciences-Chedoke Site, Hamilton, ON, Canada.

Using prospective data from the Canadian Multicentre Osteoporosis Study (CaMos), we compared health utilities index (HUI) scores after 5 years of follow-up among participants (50 years and older) with and without incident clinical fractures. Incident fractures had a negative impact on HUI scores over time. INTRODUCTION: This study examined change in health-related quality of life (HRQL) in those with and without incident clinical fractures as measured by the HUI. METHODS: The study cohort was 4,820 women and 1,783 men (50 years and older) from the CaMos. The HUI was administered at baseline and year 5. Participants were sub-divided into incident fracture groups (hip, rib, spine, forearm, pelvis, other) and were compared with those without these fractures. The effects of both time and fracture type on HUI scores were examined in multivariable regression analyses. RESULTS: Men and women with hip fractures, compared to those without, had lower HUI measures that ranged from -0.05 to -0.25. Both women and men with spine fractures had significant deficits on the pain attributes (-0.07 to -0.12). In women, self-care (-0.06), mobility and ambulation (-0.05) were also negatively impacted. Women with rib fractures had deficits similar to women with spine fractures, and these effects persisted over time. In men, rib fractures did not significantly affect HUI scores. Pelvic and forearm fractures did not substantially influence HUI scores. CONCLUSION: The HUI was a sensitive measure of HRQL change over time. These results will inform economic analyses evaluating osteoporosis therapies.

 

 

Osteoporos Int. 2008 Sep 18. [Epub ahead of print]

Nitrate use and changes in bone mineral density: the Canadian Multicentre Osteoporosis Study.

Jamal SA, Goltzman D, Hanley DA, Papaioannou A, Prior JC, Josse RG.

Medicine, University of Toronto, Toronto, ON, Canada, sophie.jamal@utoronto.ca.

Nitrates may have beneficial effects on bone. To determine if nitrates were associated with increased bone mineral density (BMD), we conducted a secondary analysis using data from subjects in a prospective study. Subjects reporting nitrate use had increased BMD compared with non-users, confirming that nitrates have positive BMD effects in women and men. INTRODUCTION: Prior studies suggest positive associations between nitrates and bone. METHODS: We used linear regression models, stratified by gender and adjusted for age, weight, and baseline differences, to determine the association between daily nitrate use and BMD among subjects participating in the Canadian Multicentre Osteoporosis Study. All results are reported as annualised percent change in BMD at the hip and spine among nitrate users compared to non-users. RESULTS: We included 1,419 men (71 reported daily nitrate use) and 2,587 women (97 reported daily nitrate use). Male non-users had decreased hip BMD (-1.3%; 95% confidence interval [95%CI] = -1.6 to -1.1) and increased spine BMD (2.8%; 95%CI = 2.5 to 3.1). Male nitrate users had increased hip BMD (1.4%; 95%CI = 0.1 to 2.8) and spine BMD (4.5%; 95%CI = 3.2 to 5.7). Among women, non-users had decreased hip BMD (-1.9; 95%CI = -2.1 to -1.7) and increased spine BMD (2.1%; 95%CI = 1.9 to 2.4) whilst users had an increase in hip BMD (2.0%; 95%CI = 1.2 to 2.8) and spine BMD (4.1%; 95%CI = 3.4 to 4.9). CONCLUSION: Nitrate use is associated with increased BMD at the hip and spine in men and women.

 

 

Blood Press Monit. 2008 Oct;13(5):277-83.

Low-dose transdermal hormone therapy does not interfere with the blood pressure of hypertensive menopausal women: a pilot study.

de Carvalho MN, Nobre F, Mendes MC, Dos Reis RM, Ferriani RA, Silva de Sá MF.

Department of Gynecology and Obstetrics. University of São Paulo, São Paulo, Brazil.

OBJECTIVES: To determine the effects of low-dose transdermal hormone therapy (HT) on systolic (SBP) and diastolic (DBP) blood pressure (BP) evaluated by 24-h ambulatory blood pressure monitoring (ABPM) in hypertensive postmenopausal women. METHODS: The study was conducted on 24 hypertensive postmenopausal women aged, on average, 54 years and under treatment with enalapril maleate (10-20 mg/day) combined or not with hydrochlorothiazide (25 mg/day). Thirteen women used a transdermal adhesive containing estradiol and norethisterone (25 and 125 mug active substance/day, respectively) and 11 did not receive HT. ABPM, lipid profile, and climacteric symptoms were evaluated before and 3 and 6 months after treatment. RESULTS: After 3 and 6 months of follow-up, there was a statistically significant reduction of the Blatt-Kupperman menopausal index in the treated group (19.6+/-8.3 vs. 9.6+/-5.9 vs. 9.7+/-7.0; P=0.01). No significant difference in any of the ABPM variables (areas under the systolic and diastolic curves, mean SBP and DBP, SBP and DBP loads and wakefulness-sleep variation) or in the lipid profile was observed between or within groups at the three time points studied. CONCLUSION: Low-dose transdermal HT administered for 6 months was effective in improving climacteric symptoms and did not change BP values or circadian pattern in postmenopausal women with mild-to-moderate arterial hypertension taking antihypertensive medications.

 

 

Ginecol Obstet Mex. 2008 May;76(5):261-6.

Osteoporosis prevalence in open population at Mexico City

De Lago Acosta A, Parada Tapia MG, Somera Iturbide J.

BACKGROUND: In Mexico there isn't accurate epidemiologic information of osteoporosis prevalence, however it is estimated that 24.5 million people are at risk or suffer it yet. OBJECTIVE: To show prevalence of osteoporosis in open population of several areas of Mexico City. PATIENTS AND METHOD: Retrospective, transversal and open study at an osseous densitometric data base information from 5,924 patients. RESULTS: Densitometry evidence that 17.9% suffer osteoporosis (79.8 female and 20.1% male), 34.5% osteopeny (76.1 female and 23.8 female), and 47.4% had normal bones (75.8% female and 24.1% female). CONCLUSIONS: Since osseous mineral density changes exponentially increases with age, osteopenic and osteoporosis index is very high after 40 years old; due to that there must be considered preventative programs for young groups, and to practice densitometries to 30 year old men and women.

 

 

J Clin Endocrinol Metab. 2008 Sep 16. [Epub ahead of print]

Breast safety and efficacy of genistein aglycone for post-menopausal bone loss: a follow-up study.

Marini H, Bitto A, Altavilla D, Burnett BP, Polito F, Di Stefano V, Minutoli L, Atteritano M, et al

Department of Biochemical, University of Messina, Italy.

CONTEXT: Genistein aglycone improves bone metabolism in women. However, questions about the long-term safety of genistein on breast as well as its continued efficacy still remain. OBJECTIVE: We assessed the continued safety profile of genistein aglycone on breast and endometrium, and its effects on bone after 3 years of therapy. DESIGN: The parent study was a randomized, double-blind, placebo-controlled trial involving 389 osteopenic, postmenopausal women for 24-months. Subsequently, a subcohort (138 patients) continued therapy for an additional year. PATIENTS AND INTERVENTIONS: Participants received 54mg of genistein aglycone daily (n=71) or placebo (n=67). Both arms received calcium and vitamin D3 in therapeutic doses. MAIN OUTCOMES: Mammographic density was assessed at baseline, 24 and 36 months by visual classification scale and digitized quantification. BRCA1 and BRCA2, sister chromatid exchange and endometrial thickness were also evaluated. Lumbar spine and femoral neck BMD were also assessed. Secondary outcomes were biochemical levels of bone markers. RESULTS: After 36 months, genistein did not significantly change mammographic breast density or endometrial thickness, BRCA1 and BRCA2 expression was preserved while sister chromatid exchange were reduced compared with placebo. BMD increases were greater with genistein for both femoral neck and lumbar spine compared to placebo. Genistein also significantly reduced PYR, as well as serum CTX and sRANKL while increasing B-ALP, IGF-I and OPG levels. There were no differences in discomfort or adverse events between groups. CONCLUSIONS: After 3-years of treatment, genistein exhibited a promising safety profile with positive effects on bone formation in a cohort of osteopenic, postmenopausal women.

 

 

Ann Epidemiol. 2008 Sep;18(9):671-7.

HDL-cholesterol and incidence of breast cancer in the ARIC cohort study.

Kucharska-Newton AM, Rosamond WD, Mink PJ, Alberg AJ, Shahar E, Folsom AR.

Department of Epidemiology, University of North Carolina at Chapel Hill, NC, USA.

PURPOSE: An association of low plasma HDL-cholesterol with risk of breast cancer has been suggested by multiple studies; the evidence, however, is not conclusive. We examined the possible association of low HDL-cholesterol with incidence of breast cancer using data from the Atherosclerosis Risk in Communities Study (ARIC) cohort, a prospective study of a randomly selected sample of women and men from four U.S. communities. METHODS: Among 7,575 female members of the ARIC cohort, 359 cases of incident breast cancer were ascertained during the follow-up from 1987 through 2000. RESULTS: In analysis adjusted for age, race, body mass index, smoking, and reproductive variables, we observed no association of low baseline HDL-cholesterol (<50mg/dL) with incident breast cancer in the total sample (hazard ratio [HR]=1.08 [95% confidence interval (CI), 0.84-1.40]) and a modest association (HR=1.67 [95% CI, 1.06-2.63]) among women who were premenopausal at baseline. No association was observed among women who were postmenopausal at baseline. Removal from analysis of the first 5 years of follow-up did not appreciably change the observed associations. CONCLUSION: Results of our study suggest that low HDL-cholesterol among premenopausal women may be a marker of increased breast cancer risk.

 

 

Menopause. 2008 Sep 10. [Epub ahead of print]

Implications of diminished ovarian reserve (DOR) extend well beyond reproductive concerns.

Pal L, Bevilacqua K, Zeitlian G, Shu J, Santoro N.

Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, CT.

OBJECTIVES:: To investigate whether a diagnosis of diminished ovarian reserve (DOR) in premenopausal years has adverse implications for skeletal health and quality of life. DESIGN:: This was a cross-sectional study of infertile, albeit healthy, mid-reproductive-age women (younger than 42 y) attending an academic infertility practice. RESULTS:: Eighty-nine women with varying causes of infertility were prospectively enrolled. Serum (cycle d 1-3) was collected for markers of ovarian reserve, bone metabolism, testosterone, and free androgen index. Bone mineral density (BMD) was assessed and categorized as low if the Z score was less than -1.0). Infertile women with DOR (n = 28) demonstrated significantly higher serum follicle-stimulating hormone levels (P < 0.001), lower müllerian-inhibiting substance (MIS) levels (P < 0.001), smaller ovarian dimensions (P < 0.05), lower testosterone levels (P = 0.035), lower free androgen index (P = 0.019), and enhanced bone metabolism (P = 0.003); although the prevalence of low BMD was higher in women with DOR who were younger than 41, this relationship was not of statistical significance (P = 0.106). Women younger than 41 years of age with DOR were significantly more likely to manifest disturbed sleep (P = 0.049) and acknowledge dissatisfaction with sexual intimacy (P = 0.004) compared with those with infertility and normal ovarian reserve. After adjustment for potential confounders, a diagnosis of DOR was significantly associated with low BMD, increased bone turnover, sexual dissatisfaction, and disturbed sleep. CONCLUSIONS:: Our data suggest that DOR unmasked in the context of infertility evaluation has adverse implications for a woman's well-being that extend well beyond the thus far appreciated reproductive concerns. A decline in ovarian hormones, specifically estrogen and testosterone, concomitant with DOR may be hypothesized as a mechanism that can explain the observed multisystem ramifications of DOR including increased bone turnover, low BMD, sexual distress, and disturbed sleep.

 

 

Selección de Resúmenes de Menopausia

Semana del 24 al 30 de Septiembre 2008

Juan Enrique Blümel. Departamento Medicina Sur. Universidad de Chile

 

 

 

 

 

Breast Cancer Res. 2008 Sep 19;10(5):R78. [Epub ahead of print]

Menopausal hormone therapy in relation to breast cancer characteristics and prognosis: a cohort study.

Rosenberg LU, Granath F, Dickman PW, Einarsdottir K, Wedren S, Persson I, Hall P.

INTRODUCTION: Menopausal hormone therapy has been reported to increase the risk of certain subtypes of breast cancer and to be associated with a favorable survival. This could either be due to an increased mammographic surveillance or a biological effect. We assessed these associations in a Swedish cohort of postmenopausal breast cancer patients holding information on mammographic examinations, menopausal hormone therapy use, other breast cancer risk factors, and cancer treatment. METHODS: We analyzed 2,660 postmenopausal women aged 50-74 years, diagnosed with invasive breast cancer in 1993-1995 and followed until the end of year 2003 (median follow-up 9 years and 3 months). We assessed the influence of hormone therapy before diagnosis on tumor characteristics and breast cancer specific survival. We analyzed hormone therapy before diagnosis by regimen (estrogen-progestin therapy or estrogen alone therapy), recency (current or past), and duration of use (<5 years or [greater than or equal to]5 years). RESULTS: Current, but not past use, compared to never use of hormone therapy before diagnosis seemed to be associated with tumors of low grade and improved breast cancer specific survival. The associations were stronger with longer duration, but did not vary significantly by regimen. The favorable survival among current users of hormone therapy was only partly explained by differences in available tumor characteristics and mammographic surveillance. CONCLUSIONS: We conclude that current menopausal hormone therapy, especially long-term, is associated with favorable tumor characteristics and survival.

 

 

J Natl Cancer Inst. 2008 Sep 23. [Epub ahead of print

Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers.

Eisen A, Lubinski J, Gronwald J, Moller P, Lynch HT, Klijn J, Kim-Sing C, Neuhausen SL, et al.

Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada

Background Hormone therapy (HT) is commonly given to women to alleviate the climacteric symptoms associated with menopause. There is concern that this treatment may increase the risk of breast cancer. The potential association of HT and breast cancer risk is of particular interest to women who carry a mutation in BRCA1 because they face a high lifetime risk of breast cancer and because many of these women take HT after undergoing prophylactic surgical oophorectomy at a young age. Methods We conducted a matched case-control study of 472 postmenopausal women with a BRCA1 mutation to examine whether or not the use of HT is associated with subsequent risk of breast cancer. Breast cancer case patients and control subjects were matched with respect to age, age at menopause, and type of menopause (surgical or natural). Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated with conditional logistic regression. Statistical tests were two-sided. Results In this group of BRCA1 mutation carriers, the adjusted OR for breast cancer associated with ever use of HT compared with never use was 0.58 (95% CI = 0.35 to 0.96; P = .03). In analyses by type of HT, an inverse association with breast cancer risk was observed with use of estrogen only (OR = 0.51, 95% CI = 0.27 to 0.98; P = .04); the association with use of estrogen plus progesterone was not statistically significant (OR = 0.66, 95% CI = 0.34 to 1.27; P = .21). Conclusion Among postmenopausal women with a BRCA1 mutation, HT use was not associated with increased risk of breast cancer; indeed, in this population, it was associated with a decreased risk.

 

 

Int J Gynaecol Obstet. 2008 Sep 22. [Epub ahead of print

Effects of hormone therapy with estrogen and/or progesterone on sleep pattern in postmenopausal women.

Hachul H, Bittencourt LR, Andersen ML, Haidar MA, Baracat EC, Tufik S.

Department of Gynecology, Federal University of São Paulo (UNIFESP/EPM), São Paulo, Brazil.

OBJECTIVE: To investigate the effects of estrogen and progesterone on sleep in postmenopausal women. METHOD: The 33 participants were randomly assigned to an estrogen or placebo group after undergoing clinical and hormonal assessments and a polysomnogram, and they underwent the same tests again after 12 weeks. Then, while still taking estrogen or placebo, they all received progesterone for another 12 weeks and underwent a final polysomnogram. RESULTS: Estrogen plus progesterone was more effective than estrogen alone in decreasing the prevalence of periodic limb movement (PLM) (8.1% vs 2.8%), hot flashes (14.2% vs 0%), and bruxism (11.1% vs 0%) at night, or somnolence and attention difficulty during the day. The prevalences of breathing irregularities, arousal from sleep, anxiety, and memory impairment were decreased in both groups following progesterone treatment. CONCLUSION: While not significantly affecting sleep quality, hormone therapy decreased the prevalence of arousal in both groups and that of PLM in the group treated with estrogen plus progesterone.

 

 

Heart Vessels. 2008 Sep;23(5):295-300. Epub 2008 Sep 20

Carotid intima-media thickness in pre-and postmenopausal women with suspected coronary artery disease.

Kablak-Ziembicka A, Przewlocki T, Tracz W, Pieniazek P, Musialek P, Sokolowski A, et al.

Institute of Cardiology, Collegium Medicum, Jagiellonian University, 31-202, Krakow, Poland.

Carotid intima-media thickness (CIMT) is an early marker of coronary artery disease (CAD). This study aimed to evaluate CIMT value for CAD prediction in pre-and postmenopausal women referred for coronary angiography with angina-like symptoms and a positive result of the treadmill test. The study comprised 321 women referred for coronary angiography with symptoms suggesting CAD. Carotid intima-media thickness was measured in common, bifurcation, and internal carotid artery, and expressed as the mean maximum value. Coronary angiography showed coronary stenosis >/=50% in 211 (65.7%) women, including 27 with regular menses (47.3 +/- 3.4 years) and 184 postmenopausal (65.8 +/- 7.2 years). Normal coronary arteries were found in 110 women: 17 (47.3 +/- 4.9 years) with regular menses and 93 postmenopausal (64.3 +/- 6.5 years). The highest CIMT values were found in postmenopausal CAD women (1.360 +/- 0.32 mm), as compared to premenopausal with CAD (1.178 +/- 0.36 mm, P = 0.005), pre-(0.860 +/- 0.23 mm, P < 0.001) and postmenopausal (1.022 +/- 0.30 mm, P < 0.001) women without CAD. Carotid intima-media thickness (P < 0.001), hyperlipidemia (P = 0.018), and myocardial infarction (P < 0.001), but not menopause itself or the number of years since menses cessation, were found to be independent CAD predictors. By receiver operating characteristic calculation, the mean maximum CIMT cut-off values discriminating CAD were lower in premenopausal (>/=0.933 mm) than in postmenopausal women (>/=1.075 mm; P < 0.05) resulting in similar sensitivity (85.2% and 82.6%) and specificity (70.6% and 69.9%). Carotid intima-media thickness is a strong CAD predictor in both pre-and postmenopausal women, in contrast to the menopausal status.

 

 

Am J Surg. 2008 Oct;196(4):505-11

Improved breast cancer survival among hormone replacement therapy users is durable after 5 years of additional follow-up.

Christante D, Pommier S, Garreau J, Muller P, LaFleur B, Pommier R.

Division of Surgical Oncology, Department of Surgery, Portland, OR, USA.

BACKGROUND: We previously reported that breast cancer patients who used hormone replacement therapy (HRT) had significantly lower stage tumors and higher survival than never-users. We present an update with longer follow-up, HRT use data, and in vitro research. METHODS: Our database of 292 postmenopausal breast cancer patients was updated to include HRT type, duration, and disease status. In vitro effects of estrogen (E) and/or medroxyprogesterone (MPA) on breast cancer cell growth were measured. RESULTS: Tumor prognostic factors were better and survival rates higher for both E and combination HRT users of any duration. Use greater than 10 years correlated with node-negative disease, mammographically detected tumors, and 100% survival. E supported minimal proliferation; MPA induced cell death; E+MPA results were similar to E alone. CONCLUSIONS: HRT users, regardless of type or duration of HRT use, continued to have higher survival rates. In vitro results supported the clinical finding that outcomes for users of E and E+MPA were similar.

 

 

Expert Opin Investig Drugs. 2008 Oct;17(10):1435-63

Statins: under investigation for increasing bone mineral density and augmenting fracture healing.

Tang QO, Tran GT, Gamie Z, Graham S, Tsialogiannis E, Tsiridis E, Linder T, Tsiridis E.

University of Leeds School of Medicine, Leeds General Infirmary Teaching Hospitals NHS Trust, Academic Department of Trauma and Orthopaedics, Leeds, LS1 3EX, UK.

BACKGROUND: Statins are 3-hydroxy-3-methylglutaryl (HMG)-CoA reductase inhibitors and have been shown to possess anti-lipidaemic properties effective in lowering cholesterol. Recent evidence has suggested beneficial pleiotropic effects, including that of fracture healing, alongside its widely accepted ability to reduce the incidence of cardiovascular disease. OBJECTIVES: A comprehensive review of the recent literature on the effect of statins on bone mineral density and fracture healing. METHODS: Medline/Ovid and EMBASE search and manual search of bibliography of key papers, on the effects of statins on bone metabolism including in vitro and in vivo studies, as well as clinical trials on the effects of statins on bone mineral density and fracture risk. RESULTS/CONCLUSIONS: There is robust in vitro and in vivo evidence to suggest the anabolic effects of statins on bone metabolism. Although evidence in patients with osteoporosis is conflicting, several studies have shown that the use of statins is associated with increases in bone mass density and reduction in fracture risk. Conflicting studies identified may be due to different routes of administration, types of statins employed and low doses used. Taken together, there is strong evidence to suggest that statins have beneficial effects on fracture healing that would support further clinical trials investigating such properties.

 

 

J Hypertens. 2008 Oct;26(10):1983-1992

Menopause does not affect blood pressure and risk profile, and menopausal women do not become similar to men.

Casiglia E, Tikhonoff V, Caffi S, Bascelli A, Schiavon L, Guidotti F, Saugo M, Giacomazzo M, et al.

Department of Clinical and Experimental Medicine, University of Padova, Padova, Italy.

OBJECTIVE: Menopause is considered to be a cardiovascular risk factor, but this belief is based on opinions rather than on evidence. Confounding effects of age are often neglected. DESIGN: Population-based study with further subanalysis of case-to-case age-matched cohorts of men and fertile and menopausal women. SETTING: Epidemiology in primary, public, institutional frame. PARTICIPANTS: Nine thousand three hundred and sixty-four men and women aged 18-70 years representative of Italian general population followed-up for 18.8 +/- 7.7 years. MAIN OUTCOME MEASURES: Blood pressure (BP), prevalence and incidence of hypertension, serum total, high-density lipoprotein and low-density lipoprotein cholesterol, glucose tolerance, body adiposity, vascular reactivity, target organ damage, overall and cardiovascular mortality and morbidity, by gender and by menopausal status. RESULTS: Cross-sectional: crude BP, pressor response to cold, orthostatic BP decrease, BMI, skinfold thickness, fasting and postload blood glucose and insulin, serum lipids, left ventricular mass, serum creatinine, microalbuminuria and augmetantion index were higher in menopausal than in fertile women, and comparable in menopausal women and men, a difference that was no longer present when adjusting for age or considering age-matched cohorts. Longitudinal: BP increase during follow-up, cardiovascular mortality and morbidity were greater in menopausal than in fertile women, and comparable in menopausal women and men, a difference no longer present in age-matched cohorts. Menopausal status was rejected from multivariate Cox analysis also including age. CONCLUSION: The cardiovascular effects usually attributed to menopause seem to be a mere consequence of the older age of menopausal women.

 

 

J Hypertens. 2008 Oct;26(10):1976-1982

Blood pressure around the menopause: a population study.

Cifkova R, Pitha J, Lejskova M, Lanska V, Zecova S.

Department of Preventive Cardiology, Institute for Clinical and Experimental Medicine, Czech Republic.

Background: Hypertension is a major cardiovascular risk factor possibly explaining the excessive cardiovascular morbidity and mortality in postmenopausal women. Cross-sectional and longitudinal studies have explored this issue with diverging results. Our study sought to elucidate the impact of the menopause on blood pressure in a representative population sample. Methods: The study involved randomly selected 908 female residents of a Prague district, aged 45-54 years (respondence rate, 63.9%). Three definitions of the menopause were used: self-reported menstrual characteristics (premenopausal with the final menstrual period less than 60 days; late menopausal transition, with final menstrual period 60-365 days; and postmenopausal, final menstrual period more than 365 days before the examination), levels of follicle-stimulating hormone (</=40 IU/l for premenopausal and more than 40 IU/l for postmenopausal women), and both. Results: Age-adjusted and BMI-adjusted systolic blood pressure and diastolic blood pressure did not differ among the groups regardless of the definition of menopause. There was also no difference in the prevalence of hypertension and in the age-adjusted and BMI-adjusted odds ratio for hypertension. Multiple regression analysis testing the association between systolic blood pressure and diastolic blood pressure, and age, BMI, heart rate, smoking, and antihypertensive medication explained a rather small proportion of the BP variation. No correlation was found between BP and age in either subgroup; the closest correlation was always found between BP and BMI. Conclusion: In our rather representative population random sample of women around the menopause, the rise in blood pressure after the menopause appeared to be due to increased BMI rather than to ovarian failure per se.

 

 

Med Clin (Barc). 2008 Sep 20;131(9):333-8

Clinical usefulness of biochemical markers of bone turnover in early postmenopausal women: two years longitudinal study.

Navarro Casado L, Blázquez Cabrera JA, Del Pino Montes J, Almar Marqués E, Cháfer Rudilla M, et al.

Laboratorio de Análisis Clínicos. Hospital General Universitario de Albacete. Albacete. España.

BACKGROUND AND OBJECTIVE: Many studies have been performed on the ability of bone turnover markers (BTM) for the prediction of bone loss and to assess the correlation of BTM with bone mineral density (BMD). However, the results from these studies have been mixed. The aim of this study was to assess the usefulness of BTM to predict bone loss and to analize the correlation of BTM with BMD in early postmenopausal women. SUBJECTS AND METHOD: 183 healthy women, aged 50 to 55 years, with natural menopause of 6 to 36 months were randomly selected. We measured bone alkaline phosphatase (BALP), intact osteocalcine (OC) and C-telopeptide (sCTx) in serum, and calcium, deoxipiridinoline (DPD) and N-telopeptide (NTx) in urine. Bone densitometry of the spine (L(2)-L(4)) was performed at the start of the study and two years later. Student t test, ANOVA, chi(2) test and ROC curves were used for the statistical analysis. RESULTS: Bone markers, mainly OC and CTx, correlated with BMD and discriminated osteoporosis, osteopenia and normal bone mass (p < 0.001). According to the ROC curves, OC had a sensitivity of 77.8% and specificity of 80.6% for the diagnosis of osteoporosis and sCTx, 83.3% and 74.5%, respectively. Regarding the relation to bone loss, only sCTx showed difference between the lowest and the highest quartile (p = 0.042), but we did not find an association between high turnover and fast bone losers. CONCLUSIONS: Bone markers, mainly OC and sCTx, are useful for identification of osteoporotic and osteopenic early postmenopausal women. However, regarding the bone loss, only CTx has a weak predictive value.

 

 

Int J Gynaecol Obstet. 2008 Sep 20. [Epub ahead of print

Isosorbide mononitrate versus alendronate for postmenopausal osteoporosis.

Nabhan AF, Rabie NH.

Department of Obstetrics and Gynecology, University of Ain Shams, Cairo, Egypt.

OBJECTIVE: To compare the effectiveness, safety, and affordability of isosorbide mononitrate with alendronate for postmenopausal osteoporosis. METHODS: A randomized controlled trial of 60 postmenopausal women with osteoporosis. Participants were randomly assigned to receive either 20 mg daily of isosorbide mononitrate or 70 mg weekly of alendronate for 12 months. Bone mineral density (BMD) was measured using dual X-ray absorptiometry (DXA) at baseline and after 12 months. RESULTS: Both groups showed significant improvement in BMD. Isosorbide mononitrate yielded a comparable effect to alendronate for BMD and T-score at the end of the follow-up period. For BMD and T score the mean differences between the 2 groups were -0.005 (95% CI, -0.02 to 0.03) and 0.31 (95% CI, -0.03 to 0.64), respectively. A 10.8% and 12.1% change in BMD after 12 months was seen for isosorbide mononitrate and alendronate, respectively. CONCLUSION: Isosorbide mononitrate is comparable to alendronate. Nitric oxide donors may be an effective and affordable therapy to improve bone mineral density.