Female Menopause – All Phases

Women experience two phases—perimenopause and menopause. The latter is the ending stage of menses; therefore, “post menopause” technically doesn’t exist.  Patients evidence a wide range of symptoms, which can be assuaged with hormone modulation. Some studies suggest an “androgen” deficiency, which if treated can positively affect a sense of well-being and also restore sexual desire. Review current research and medical articles on female menopause to better help your female patients.


Combination Hormone Replacement Therapy Linked to Lower-Risk Breast Cancers.pdf

The types of breast tumors that occur after combination hormone replacement therapy in the peri- and post-menopausal period tend to have a better prognosis than those that occur after estrogen-only replacement therapy, Swedish researchers report.
(2006, May 9). Combination hormone replacement therapy linked to lower-risk breast cancers [Electronic version]. Reuters Health. Retrieved May 31, 2007.

Hormones and Sexuality During Transition to Menopause.pdf

This study confirms the observation that sexual dysfunction increases over the menopausal transition. Several factors associated with sexual dysfunction include low DHEAS, absence of a sexual partner, anxiety, and children under the age of 18 living at home.
Gracia, C.R., Freeman, E.W., Sammel, M.D., Lin, H. & Mogul, M. (2007). Hormones and sexuality during transition to menopause [Electronic version]. Obstetrics and Gynecology, 109(4), 831-840. Retrieved May 31, 2007.

NAMS Updates Recommendations on Diagnosis and Management of Osteoporosis in Postmenopausal Women.pdf

To address the need for standards of care as they relate to menopause-associated health conditions, the North American Menopause Society (NAMS) has updated its evidence-based guidelines on the diagnosis, prevention, and treatment of osteoporosis in postmenopausal women. The full report was published in the May/June 2006 issue of Menopause.
Armstrong, C. (2006, November 1). NAMS updates recommendations on diagnosis and management of osteoporosis in postmenopausal women [Electronic version]. American Family Physician, 74(9). Retrieved November 2, 2006.

Serum Leptin Concentrations in Pre- and Postmenopausal Women on Sex Hormone Therapy.pdf

According to this study, Endogenous E(2) and androgens in premenopausal women and estrogen and estrogen-progestin therapies in postmenopausal subjects do not influence serum leptin concentrations. Leptin level is related to body mass and BMI, but not to sex hormone status. The distribution of adipose tissue and the type of obesity (android or gynoid) have no influence on serum leptin concentration. The correlation between serum leptin level and blood pressure requires further investigation.
Bednarek-Tupikowska, G., Filus, A., Kuliczkowska-Plaksej, J., Tupikowski, K., Bohdanowicz-Pawlak, A. &  Milewicz, A. (2006). Serum leptin concentrations in pre- and postmenopausal women on sex hormone therapy. [Electronic version]. Gynecological Endocrinology, 22(4), 207-212. Retrieved November 27, 2006.

Soy Isoflavones Affect Platelet Thromboxane A2 Receptor Density But Not Plasma Lipids in Menopausal Women.pdf

This study demonstrated that the beneficial effects of isoflavones in menopausal women could be more related to platelet function than to improving classical cardiovascular risk factors.
Garrido, A., De la Maza, M.P., Hirsch, S. & Valladares, L. (2006). Soy isoflavones affect platelet thromboxane A2 receptor density but not plasma lipids in menopausal women [Electronic version]. Maturitas, 54(3), 270-276. Epub January 18, 2006. Retrieved November 27, 2006.

Testosterone Aromatization and Cognition in Women: A Randomized, Placebo-Controlled Trial.pdf

This study did not observe any effects of aromatase inhibition on cognition in healthy, estrogen-treated postmenopausal women treated with testosterone. This may be due to insufficient study power or a true lack of effect. However, the findings highlight that the detection of subtle changes in cognition in well women require the development of sensitive instruments and large randomized, controlled trials.
Shah, S., Bell, R.J., Savage, G., Goldstat, R., Papalia, M.A., Kulkarni, J., et al. (2006). Testosterone aromatization and cognition in women: a randomized, placebo-controlled trial [Electronic version]. Menopause, 13(4), 600-608. Retrieved November 27, 2006.

Combined Estrogen and Testosterone Use and Risk of Breast Cancer in Postmenopausal Women.pdf

According to this study, consistent with the elevation in risk for endogenous testosterone levels, women using estrogen and testosterone therapies have a significantly increased risk of invasive breast cancer.
Tamimi, R.M., Hankinson, S.E., Chen, W.Y., Rosner, B.. & Colditz, G.A. (2006). Combined estrogen and testosterone use and risk of breast cancer in postmenopausal women [Electronic version]. Archives of Internal Medicine, 166(14), 1483-1489. Retrieved November 14, 2006.

Safety and Adverse Effects of Androgens: How to Counsel Patients.pdf

In short-term clinical trials of androgen replacement in women, several benefits have been shown, including improved libido, bone mineral density and body composition. While androgen therapy for women is relatively new, it is receiving more attention.
Basaria, S. & Dobs, A.S. (2004). Safety and adverse effects of androgens: how to counsel patients [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S25-32. Retrieved May 18, 2005.

Experts Consider HT for Younger Women.pdf

Questions still persist after the release of the July 2002 Women’s Health Initiative findings regarding hormone therapy.  Researchers have been looking at the data to see if certain changes in dosage or initiation age could still provide benefits to women.
Elliott, V.S., (2005, February 28). Experts consider HT for younger women [Electronic version]. American Medical News, pp. 19-20.  Retrieved April 28, 2005.

Effects of Estrogen with and without Progestin on Urinary Incontinence.pdf

The conclusion of this study was that conjugated equine estrogen alone and CEE + MPA increased the risk of UI among continent women and worsened the characteristics of UI among symptomatic women after 1 year. Conjugated equine estrogen with or without progestin should not be prescribed for the prevention
Hendrix, S.L., Cochrane, B.B., Nygaard, I.E., Handa, V.L., Barnabei, V.M., Iglesia, C., et al. (2005). Effects of estrogen with and without progestin on urinary incontinence [Electronic version]. The Journal of the American Medical Association, 293(8), 935-948. Retrieved November 18, 2005.

Levels of Serum C-Reactive Protein During Oral and Transdermal Estradiol in Postmenopausal Women with and without a History of Intrahepatic Cholestasis of Pregnancy.pdf

This study concluded that the synthesis of CRP is not affected by a history of ICP. It is readily and dose dependently stimulated by oral but not by transdermal E2 in as soon as 2 wk.
Ropponen, A., Aittomaki, K., Tikkanen, M.J. & Ylikorkala, O. (2005). Levels of serum c-reactive protein during oral and transdermal estradiol in postmenopausal women with and without a history of intrahepatic cholestasis of pregnancy [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 90(1), 142-146. Retrieved November 18, 2005.

Predictors of Decreased Libido in Women During the Late Reproductive Years.pdf

This study concluded that decreased libido in the late reproductive years is associated with a pronounced fluctuation in total testosterone over time. Other independent risk factors for decreased libido include vaginal dryness, depression, and living with children. Sexual dysfunction is a complex disorder, related to physiological and psychosocial factors, requiring further investigation.
Gracia, C.R., Sammel, M.D., Freeman, E.W., Liu, L., Hollander, L. & Nelson, D.B. (2004). Predictors of decreased libido in women during the late reproductive years [Electronic version]. Menopause, 11(2), 144-150. Retrieved May 8, 2007.

HRT Scare Study Was Flawed, Say Scientists.pdf

According to a group of leading researchers, the American study that triggered a worldwide scare over the risks of Hormone Replacement Therapy was fundamentally flawed and not applicable to most women going through the menopause.
Derbyshire, D. (2004, June 28). HRT scare study was flawed, say scientists [Electronic version]. Daily Telegraph. Retrieved August 31, 2004.

Effects of Conjugated Equine Estrogen in Postmenopausal Women with Hysterectomy: The Women's Health Initiative Randomized Controlled Trial.pdf

According to this study, the use of CEE increases the risk of stroke, decreases the risk of hip fracture, and does not affect CHD incidence in postmenopausal women with prior hysterectomy over an average of 6.8 years. A possible reduction in breast cancer risk requires further investigation. The burden of incident disease events was equivalent in the CEE and placebo groups, indicating no overall benefit. Thus, CEE should not be recommended for chronic disease prevention in postmenopausal women.
Anderson, G.L., Limacher, M., Assaf, A.R., Bassford, T., Beresford, S.A., Black, H., et al. (2004). Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women's Health Initiative Randomized Controlled Trial [Electronic version]. The Journal of the American Medical Association, 291(14), 1701-1712. Retrieved November 21, 2005.

Formulations and Use of Androgens in Women.pdf

The use of androgen therapy for postmenopausal women is discussed in this article. It suggests that the goal of androgen treatment should be to achieve normal premenopausal levels of testosterone, thus limiting adverse effects and adverse experiences.
Chu, M.C. & Lobo, R.A. (2004). Formulations and use of androgens in women. [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S3-7. Retrieved May 18, 2005.

Conjugated Equine Estrogens and Global Cognitive Function in Postmenopausal Women: Women's Health Initiative Memory Study.pdf

According to this study, for women aged 65 years or older, hormone therapy had an adverse effect on cognition, which was greater among women with lower cognitive function at initiation of treatment.
Espeland, M.A., Rapp, S.R., Shumaker, S.A., Brunner, R., Manson, J.E., Sherwin, B.B., et al. (2004). Conjugated equine estrogens and global cognitive function in postmenopausal women: Women's Health Initiative Memory Study [Electronic version]. The Journal of the American Medical Association, 291(24), 2959-2968. Retrieved November 21, 2005.

The Women’s Health Initiative 2004 – Review and Critique.pdf

This article reviews the published results from the Women’s Health Initiative (WHI) and their various interpretations. The WHI was designed to define the risks and benefits of interventions, notably hormone therapy, to potentially prevent heart disease, breast and colorectal cancer, and osteoporotic fractures in postmenopausal women.
Goldman, J.A. (2004). The Women’s Health Initiative 2004 – Review and Critique [Electronic version]. Medscape General Medicine, 6(3). Retrieved September 27, 2005.

Evidence that Androgenic and Estrogenic Metabolites Contribute to the Effects of Dehydroepiandrosterone on Cognition in Postmenopausal Women.pdf

The results of this study help, in part, to explain DHEA's complex effects on cognition. The diverse effects of sex steroids across tasks underscore the importance of identifying the specific cognitive mechanisms influenced by sex steroids and emphasizes that one should not expect sex steroids to produce homogeneous effects across cognitive tasks.
Hirshman, E., Merritt, P., Wang, C.C., Wierman, M., Budescu, D.V., Kohrt, W., et al. (2004). Evidence that androgenic and estrogenic metabolites contribute to the effects of dehydroepiandrosterone on cognition in postmenopausal women [Electronic version]. Hormones and Behavior, 45(2), 144-155. Retrieved November 21, 2005.

Potential Anabolic Effects of Androgens on Bone.pdf

With the decrease of estrogen at menopause, the need for androgens increases in post-menopausal women.  Androgens also appear to be important for the bone health of women who are pre-menopausal.
Kearns, A.E. & Khosla, S. (2004). Potential anabolic effects of androgens on bone [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S14-18. Retrieved May 18, 2005.

Review of the Book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.pdf

Review by Amazon.com of Suzanne Somers’ book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.
Lightner, J. (2004). [Review of the book The sexy years: Discover the hormone connection: the secret to fabulous sex, great health, and vitality, for women and men]. Retrieved September 10, 2004.

Hot Flashes and Androgens: A Biological Rationale for Clinical Practice.pdf

This article discusses the important role androgens play in the treatment of hot flashes.  It also emphasizes the need to individualize treatment for menopausal women.
Notelovitz, M. (2004). Hot flashes and androgens: a biological rationale for clinical practice [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S8-13. Retrieved May 18, 2005.

Low Androgenization Index in Elderly Women and Elderly Men with Alzheimer's Disease.pdf

The authors of this study investigated whether testosterone levels and testosterone availability differ between older lean subjects with and without Alzheimer's disease (AD). Sex hormone binding globulin (SHBG) and estradiol levels were higher, whereas the free androgenization index (FAI) was lower, in lean subjects with AD than in lean subjects without AD. Factors involved in the increase of SHBG secretion could have an important role in the lower testosterone availability of subjects with AD.
Paoletti, A.M., Congia, S., Lello, S., Tedde, D., Orru, M., et al. (2004). Low androgenization index in elderly women and elderly men with Alzheimer's disease [Electronic version]. Neurology. 62(2), 301-303. Retrieved September 27, 2005.

The Role of Androgens in Female Sexual Dysfunction.pdf

Although there are no FDA-approved androgen therapies at this time, increased attention is being paid to low androgen concentrations in the treatment of female sexual dysfunction (FSD).
Shifren, J.L. (2004). The role of androgens in female sexual dysfunction [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S19-24. Retrieved May 18, 2005.

Conjugated Equine Estrogens and Incidence of Probable Dementia and Mild Cognitive Impairment in Postmenopausal Women: Women's Health Initiative Memory Study.pdf

This study concluded that estrogen therapy alone did not reduce dementia or MCI incidence and increased the risk for both end points combined. Pooling data for estrogen alone and estrogen plus progestin resulted in increased risks for both end points. Use of hormone therapy to prevent dementia or cognitive decline in women 65 years of age or older is not recommended.
Shumaker, S.A., Legault, C., Kuller, L., Rapp, S.R., Thal, L., Lane, D.S., et al. (2004). Conjugated equine estrogens and incidence of probable dementia and mild cognitive impairment in postmenopausal women: Women's Health Initiative Memory Study [Electronic version]. The Journal of the American Medical Association, 291(24), 2947-2958. Retrieved November 21, 2005.

Effects of Estrogen Plus Progestin on Risk of Fracture and Bone Mineral Density: The Women's Health Initiative Randomized Trial

This study demonstrates that estrogen plus progestin increases BMD and reduces the risk of fracture in healthy postmenopausal women. The decreased risk of fracture attributed to estrogen plus progestin appeared to be present in all subgroups of women examined. When considering the effects of hormone therapy on other important disease outcomes in a global model, there was no net benefit, even in women considered to be at high risk of fracture.
Cauley, J.A., Robbins, J., Chen, Z., Cummings, S.R., Jackson, R.D., LaCroix, A.Z., et al. (2003). Effects of estrogen plus progestin on risk of fracture and bone mineral density: The Women's Health Initiative Randomized Trial [Electronic version]. The Journal of the American Medical Association, 290(13), 1729-1738. Retrieved December 7, 2005.

Influence of Estrogen Plus Progestin on Breast Cancer and Mammography in Healthy Postmenopausal Women: The Women's Health Initiative Randomized Trial.pdf

This study concluded that relatively short-term combined estrogen plus progestin use increases incident breast cancers, which are diagnosed at a more advanced stage compared with placebo use, and also substantially increases the percentage of women with abnormal mammograms. These results suggest estrogen plus progestin may stimulate breast cancer growth and hinder breast cancer diagnosis.
Chlebowski, R.T., Hendrix, S.L., Langer, R.D., Stefanick, M.L., Gass, M., Lane, D., et al. (2003). Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women: The Women's Health Initiative Randomized Trial [Electronic version]. The Journal of the American Medical Association, 289(24), 3243-3253. Retrieved December 7, 2005.

Hormone Replacement Therapy in Rheumatoid Arthritis is Associated with Lower Serum Levels of Soluble IL-6 Receptor and Higher Insulin-Like Growth Factor 1.pdf

The aim of this study was to investigate the effects of HRT on the serum levels of hormones and cytokines regulating bone turnover in 88 postmenopausal women with active rheumatoid arthritis (RA) randomly allocated to receive HRT plus calcium and vitamin D3 or calcium and vitamin D3 alone for 2 years.
D'Elia, H.F., Mattsson, L.A., Ohlsson, C., Nordborg, E. & Carlsten, H. (2003). Hormone replacement therapy in rheumatoid arthritis is associated with lower serum levels of soluble IL-6 receptor and higher insulin-like growth factor 1 [Electronic version]. Arthritis Research & Therapy, 5(4), R202-209. Epub 2003, May 1. Retrieved October 25, 2005.

Growth Hormone Increases Bone Mineral Content in Postmenopausal Osteoporosis: A Randomized Placebo-Controlled Trial.pdf

This study concluded that bone mineral content increased to 14% with GH treatment on top of HRT and calcium/vitamin D in postmenopausal women with osteoporosis. There seems to be a delayed, extended, and dose-dependent effect of GH on bone. Thus, GH could be used as an anabolic agent in osteoporosis.
Landin-Wilhelmsen, K., Nilsson, A., Bosaeus, I. & Bengtsson, B.A. (2003). Growth hormone increases bone mineral content in postmenopausal osteoporosis: a randomized placebo-controlled trial [Electronic version]. Journal of Bone Mineral Research, 18(3), 393-405. Retrieved December 7, 2005.

Endogenous Hormones and Bone Turnover Markers in Pre- and Perimenopausal Women: SWAN.pdf

This study tested the hypothesis that higher serum osteocalcin and urinary N-telopeptide of type I collagen (NTx) concentrations would be found in women with increasing cycle irregularity or increased follicle stimulating hormone concentrations. It concluded that in these pre- and early perimenopausal women, higher FSH concentrations, but not other serum reproductive hormone concentrations, are positively associated with greater bone turnover prior to the last menstrual period.
Sowers, M.R., Greendale, G.A., Bondarenko, I., Finkelstein, J.S., Cauley, J.A., Neer, R.M., et al. (2003). Endogenous hormones and bone turnover markers in pre- and perimenopausal women: SWAN [Electronic version]. Osteoporosis International, 14(3), 191-197. Epub April 11, 2003. Retrieved November 27, 2006.

The Cardiovascular Risk of Adult GH Deficiency (GHD) Improved After GH Replacement and Worsened in Untreated GHD: A 12-Month Prospective Study.pdf

This study concluded that 12 months of GH replacement normalized IGF-I and improved lipid profile and cardiac performance in adult GHD patients. A similar period of GH deprivation induced a further impairment of lipid profile and cardiac performance. This finding strongly supports the need of GH replacement in adult GHD patients.
Colao, A., di Somma, C., Pivonello, R., Cuocolo, A., Spinelli, L., et al. (2002).  The cardiovascular risk of adult GH deficiency (GHD) improved after GH replacement and worsened in untreated GHD: a 12-month prospective study [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 87(3), 1088-1093. Retrieved September 26, 2005.

The Effects of Tibolone on Mood and Libido.pdf

According to this paper, published studies indicate beneficial effects of tibolone on both libido and mood, which otherwise significantly compromise physical, psychological, and social well-being. Hence, tibolone provides another option for menopausal women experiencing loss of libido as part of their symptomatology or who have persistent low libido despite adequate estrogen/progestin replacement therapy.
Davis, S.R. (2002). The effects of tibolone on mood and libido [Electronic version]. Menopause, 9(3), 162-170. Retrieved October 3, 2005.

Reduced Capillary Permeability and Capillary Density in the Skin of GH-Deficient Adults: Improvement After 12 Months GH Replacement.pdf

A study involving seven normotensive, nondiabetic GH-deficient adults (two women) evaluated skin capillary permeability and capillary density.  It found that the growth hormone deficiency syndrome is associated with microvascular alterations, which are responsive to growth hormone replacement.
Oomen, P.H., Beentjes, J.A., Bosma, E., Smit, A.J., Reitsma, W.D. & Dullaart, R.P. (2002). Reduced capillary permeability and capillary density in the skin of GH-deficient adults: improvement after 12 months GH replacement [Electronic version]. Clinical Endocrinology (Oxford), 56(4), 519-524. Retrieved May 18, 2005.

Risks and Benefits of Estrogen Plus Progestin in Healthy Postmenopausal Women.pdf

This study concluded that overall health risks exceeded benefits from use of combined estrogen plus progestin for an average 5.2-year follow-up among healthy postmenopausal US women. All-cause mortality was not affected during the trial. The risk-benefit profile found in this trial is not consistent with the requirements for a viable intervention for primary prevention of chronic diseases, and the results indicate that this regimen should not be initiated or continued for primary prevention of CHD.
Rossouw, J.E., Anderson, G.L., Prentice, R.L., LaCroix, A.Z., Kooperberg, C., Stefanick, M.L., et al. (2002). Risks and benefits of estrogen plus progestin in healthy postmenopausal women [Electronic version]. The Journal of the American Medical Association, 288(3), 321-333. Retrieved December 7, 2005.

Hormone Replacement Therapy, Insulin Sensitivity, and Abdominal Obesity in Postmenopausal Women.pdf

The authors concluded that postmenopausal women taking oral estrogen or those taking a combination of estrogen and HRT are more insulin-resistant than women not on HRT, even when women are of comparable total and abdominal adiposity.
Ryan, A.S., Nicklas, B.J. & Berman, D.M. (2002). Hormone replacement therapy, insulin sensitivity, and abdominal obesity in postmenopausal women [Electronic version]. Diabetes Care, 25(1), 127-133. Retrieved January 19, 2006.

Interaction of Dietary Folate Intake, Alcohol, and Risk of Hormone Receptor-Defined Breast Cancer in a Prospective Study of Postmenopausal Women.pdf

This study examined the interaction of alcohol and low folate intake on the risk of postmenopausal breast cancer stratified by tumor receptor status for estrogen (ER) and progesterone (PR). Because the results were limited primarily to ER- tumors, one plausible interpretation of these data is that alcohol influences breast cancer through its metabolite, acetaldehyde, rather than through effects on ER levels and receptor-mediated pathways.
Sellers, T.A., Vierkant, R.A., Cerhan, J.R., Gapstur, S.M., Vachon, C.M., Olson, J.E., et al. (2002). Interaction of dietary folate intake, alcohol, and risk of hormone receptor-defined breast cancer in a prospective study of postmenopausal women [Electronic version]. Cancer Epidemiology, Biomarkers & Prevention, 11(10 Pt. 1), 1104-1107. Retrieved October 3, 2005.

Androgen Replacement in Menopause.pdf

This article discusses how interest is increasing in the use of androgen replacement not only for women who have undergone premature or surgical menopause but also for those who experience natural menopause and premenopausal loss of libido from diminished free testosterone.
Burd, I.D. & Bachmann, G.A. (2001). Androgen replacement in menopause [Electronic version]. Current Women’s Health Report, 1(3), 202-205. Retrieved October 3, 2005.

Association of IGF-I Levels with Muscle Strength and Mobility in Older Women.pdf

This article summarizes that in a study population including frail and healthy older women, low IGF-I levels were associated with poor knee extensor muscle strength, slow walking speed, and self-reported difficulty with mobility tasks. These findings suggest a role for IGF-I in disability as well as a potential target population for interventions to raise IGF-I levels.
Cappola, A.R., Bandeen-Roche, K., Wand, G.S., Volpato, S. & Fried, L.P. (2001). Association of IGF-I levels with muscle strength and mobility in older women [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 86(9), 4139-4146. Retrieved September 28, 2005.

What are "Normal" Testosterone Levels for Women?.pdf

In this Letter to the Editor, the authors conclude that the role of androgens in women is becoming increasingly more recognized and established. Certainly, the use of androgens, particularly testosterone, has been shown to influence life aspects, such as mood, women’s general well being and restoration of sexual desire. However, there is limited data establishing normal androgen values for women of differing ages, to enable us to define those with "androgen deficiency." They say it is, therefore, necessary to highlight the incongruencies and short-comings of the paper by Laughlin et al. (Laughlin G, Barrett-Connor E, Kritz-Silverstein D, Von Muhlen D. 2000 Hysterectomy, oophorectomy, and endogenous sex hormone levels in older women: the Rancho Bernado Study. J Clin Endocrinol Metab. 85:645–651), and the need for larger prospective studies to establish the variations in testosterone levels in women with age.
Davis, S. & Tran, J. (2001). What are "normal" testosterone levels for women? [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 86(4), 1842-1844. Retrieved October 3, 2005.

Bone Mineral Density Response to Estrogen Replacement in Frail Elderly Women: A Randomized Controlled Trial.pdf

This study concluded that in physically frail elderly women, 9 months of HRT significantly increased BMD compared with placebo in clinically important skeletal regions. Further studies are needed to determine whether these osteogenic effects of HRT in elderly women are associated with a reduction in osteoporotic fractures.
Villareal, D.T., Binder, E.F., Williams, D.B., Schechtman, K.B, Yarasheski, K.E. & Khort, W.M. (2001). Bone mineral density response to estrogen replacement in frail elderly women: a randomized controlled trial [Electronic version]. The Journal of the American Medical Association, 286(7), 815-820. Retrieved December 14, 2006.

Sexuality Among Older Women.pdf

According to this article, in addition to hormonal changes with aging, disease and associated medications may also negatively affect sexuality. Determining the impact of medications, both alone and in combination with others, on quality of life must be considered when providing comprehensive care for elderly patients.
Gelfand, M.M. (2000). Sexuality among older women [Electronic version]. Journal of Women’s Health and Gender-Based Medicine, 9(Suppl. 1), S15-20. Retrieved October 3, 2005.

A Switch from Oral (2 mg/day) to Transdermal (50 microg/day) 17Beta-Estradiol Therapy Increases Serum Insulin-Like Growth Factor-I Levels in Recombinant Human Growth Hormone (GH)-Substituted Women with GH Deficiency.pdf

The results of the present study suggest that the potency of GH is altered in patients on transdermal compared to oral estradiol therapy. Further investigation should be undertaken to answer the question whether the increase in serum IGF-I levels is due to lower serum levels of estradiol or to differences in the mode of administration of estradiol.
Janssen, Y.J., Helmerhorst, F., Frolich, M. & Roelfsema, F. (2000). A switch from oral (2 mg/day) to transdermal (50 microg/day) 17beta-estradiol therapy increases serum insulin-like growth factor-I levels in recombinant human growth hormone (GH)-substituted women with GH deficiency [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 85(1), 464-467. Retrieved October 3, 2005.

Hysterectomy, Oophorectomy, and Endogenous Sex Hormone Levels in Older Women: The Rancho Bernardo Study.pdf

This study examines the cross-sectional association of hysterectomy and oophorectomy status, chronological age, and years since menopause with plasma levels of total and bioavailable testosterone and estradiol, androstenedione, estrone, and sex hormone-binding globulin (SHBG) in community-dwelling postmenopausal women who were not using estrogen replacement therapy.
Laughlin, G.A., Barrett-Connor, E., Kritz-Silverstein, D. & von Muhlen, D. (2000). Hysterectomy, oophorectomy, and endogenous sex hormone levels in older women: the Rancho Bernardo Study [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 85(2), 645-651. Retrieved October 3, 2005.

The Effects of Systemic Hormonal Replacement Therapy on the Skin of Postmenopausal Women.pdf

The aim of this study was to determine the effects of hormonal replacement therapy on the skin of postmenopausal women. It concluded that hormonal replacement for climacterics increases skin collagen content.
Sauerbronn, A.V., Fonseca, A.M., Bagnoli, V.R., Saldiva, P.H. & Pinotti, J.A. (2000). The effects of systemic hormonal replacement therapy on the skin of postmenopausal women [Electronic version]. International Journal of Gynaecology and Obstetrics, 68(1), 35-41. Retrieved January 4, 2006.

Gender Difference in Insulin-Like Growth Factor I Response to Growth Hormone (GH) Treatment in GH-Deficient Adults:  Role of Sex Hormone Replacement.pdf

The present study confirms short-term data published in the literature on a sex difference in rhGH dose requirement in GH-deficient patients. It furthers extends the data by demonstrating that this sex difference in GH responsivity persists and changes during the 24 months of the study. Moreover, it shows that estrogen replacement blunts the IGF-I response to rhGH in women, whereas in men with androgen substitution the responsivity increases over time, thus bearing a risk of undertreatment in women and overtreatment in men.
Span, J.P., Pieters, G.F., Sweep, C.G., Hermus, A.R. & Smals, A.G. (2000). Gender difference in insulin-like growth factor I response to growth hormone (GH) treatment in GH-deficient adults:  role of sex hormone replacement [Electronic version].  The Journal of Clinical Endocrinology & Metabolism, 85(3), 1121-1125. Retrieved September 26, 2005.

The Effects of Treatment and the Individual Responsiveness to Growth Hormone (GH) Replacement Therapy in 665 GH-Deficient Adults. KIMS Study Group and the KIMS International Board.pdf

The data from this study highlight the value of large longitudinal surveillance databases in defining the optimum dose regimen for GH replacement and indicate that women may need a higher replacement dose of GH than men.
Bengtsson, B.A., Abs, R., Bennmarker, H., Monson, J.P., Feldt-Rasmussen, U., et al. (1999). The effects of treatment and the individual responsiveness to growth hormone (GH) replacement therapy in 665 GH-deficient adults. KIMS Study Group and the KIMS International Board [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 84(11), 3929-3935. Retrieved September 26, 2005.

The Effect of Hormonal Replacement Therapy on the Vascular Reactivity and Endothelial Function of Healthy Individuals and Individuals with Type 2 Diabetes.pdf

This study concludes that menopausal status and type 2 diabetes are associated with impaired microvascular reactivity. HRT substantially improves microvascular reactivity in postmenopausal healthy women. In contrast, the effect of HRT on the microvascular reactivity of postmenopausal diabetic women is less apparent. However, the use of HRT among women with diabetes is associated with lower sICAM levels, suggesting an attenuation in endothelial activation.
Lim, S.C., Caballero, A.E., Arora, S., Smakowski, P., Bashoff, E.M., Brown, F.M., et al. (1999). The effect of hormonal replacement therapy on the vascular reactivity and endothelial function of healthy individuals and individuals with type 2 diabetes [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 84(11), 4159-4164. Retrieved January 19, 2006.

Hormone Replacement Therapy and the Risk of Colorectal Cancer: A Meta-Analysis.pdf

This article concludes that the risk of colon cancer may be decreased among recent postmenopausal HRT users. Although data are limited, the risk of fatal colon cancer also may be lower in HRT users.
Nanda, K., Bastian, L.A., Hasselblad, V. & Simel, D.L. (1999). Hormone replacement therapy and the risk of colorectal cancer: a meta-analysis [Electronic version]. Obstetrics and Gynecology, 93(5 Pt. 2), 880-888. Retrieved October 3, 2005.

Postmenopausal Estrogen Replacement Therapy and Risk of AD: A Population-Based Study.pdf

The objective was to study the association between estrogen replacement therapy in postmenopausal women and AD using a case-control design. These results from a population-based study suggest that estrogen replacement therapy is associated with a reduced risk of AD in postmenopausal women.
Waring, S.C., Rocca, W.A., Petersen, R.C., O'Brien, P.C., Tangalos, E.G. & Kokmen, E. (1999). Postmenopausal estrogen replacement therapy and risk of AD: a population-based study [Electronic version]. Neurology, 52(5), 965-970. Retrieved October 3, 2005.

A Randomized Controlled Trial of Four Doses of Transdermal Estradiol for Preventing Postmenopausal Bone Loss.pdf

This study concluded that transdermal E2 at doses of 0.025, 0.05, 0.06, and 0.1 mg/day effectively prevented bone loss in postmenopausal women.
Weiss, S.R., Ellman, H. & Dolker, M. (1999). A randomized controlled trial of four doses of transdermal estradiol for preventing postmenopausal bone loss. Transdermal Estradiol Investigator Group [Electronic version]. Obstetrics and Gynecology, 94(3), 330-336. Retrieved September 14, 2005.

Growth Hormone Deficiency in Adulthood and the Effects of Growth Hormone Replacement: A Review.pdf

The importance of GH throughout adult life is now unequivocally accepted.  GH deficiency is recognized to result in alterations in body composition, physical performance, psychological well-being, and substrate metabolism.  Many of these alterations can be improved or corrected with GH replacement.  The prospect of GH replacement becoming routine, however, does raise a number of issues.
Carroll, P.V., Christ, E.R., Bengtsson, B.A., Carlsson, L., Christiansen, J.S., et al.  (1998). Growth hormone deficiency in adulthood and the effects of growth hormone replacement: A review [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 83(2), 382-395. Retrieved May 17, 2005.

The Route of Estrogen Replacement Therapy Confers Divergent Effects on Substrate Oxidation and Body Composition in Postmenopausal Women.pdf

This article summarizes that when compared with the transdermal route, oral estrogen reduces lipid(ox), increases fat mass, and reduces lean body mass. The route of estrogen therapy confers distinct and divergent effects on substrate oxidation and body composition. The suppression of lipidox during oral estrogen therapy may increase fat mass although the fall in IGF-I may lead to a loss of lean body mass. The route-dependent changes in body composition observed during estrogen replacement therapy may have important implications for postmenopausal health.
O’Sullivan, A.J., Crampton, L.J., Freund, J. & Ho, K.K. (1998). The route of estrogen replacement therapy confers divergent effects on substrate oxidation and body composition in postmenopausal women [Electronic version]. The Journal of Clinical Investigation, 102(5), 1035-1040. Retrieved October 3, 2005.

Postmenopausal Hormone Therapy. Is it Useful for Coronary Prevention?.pdf

This article states that because about one of two U.S. women die from cardiovascular disease (heart disease and stroke), emphasis is warranted on available data, which suggest that the group of women likely to experience the greatest cardioprotection from hormone therapy are those with defined coronary disease or those at high risk for occurrence; the group of women least likely to benefit are those at increased risk for breast cancer
Wenger, N.K. (1998). Postmenopausal hormone therapy. Is it useful for coronary prevention? [Electronic version]. Cardiology Clinics, 16(1), 17-25. Retrieved October 3, 2005.

Does Estrogen Prevent Skin Aging? Results from the First National Health and Nutrition Examination Survey (NHANES I).pdf

Wrinkling, dryness and atrophy were examined in this study of 3875 postmenopausal women.  The goal of the study was to determine the possible effects estrogen has on all three skin conditions.  It was concluded that the results strongly suggest that estrogen use prevents dry skin and wrinkling associated with aging.
Dunn, L.B., Damesyn, M., Moore, A.A., Reuben, D.B. & Greendale, G.A. (1997). Does estrogen prevent skin aging? Results from the First National Health and Nutrition Examination Survey (NHANES I) [Electronic version]. Archives of Dermatology, 133(3), 339-342. Retrieved May 18, 2005.

Does Hormonal Skin Aging Exist? A Study of the Influence of Different Hormone Therapy Regimens on the Skin of Postmenopausal Women Using Non-Invasive Measurement Techniques.pdf

Non-invasive techniques were used to study the skin properties of postmenopausal women.  The study included women using hormone replacement therapy (HRT) and and some who were not being treated with HRT.  It concluded that the women who were receiving HRT had greater skin thickness and causal level than the untreated women.
Callens, A., Vaillant, L., Lecomte, P., Berson, M., Gall, Y. & Lorette, G. (1996). Does hormonal skin aging exist? A study of the influence of different hormone therapy regimens on the skin of postmenopausal women using non-invasive measurement techniques [Electronic version]. Dermatology, 193(4), 289-294. Retrieved May 18, 2005.

Metabolic Effects of 12-Month Percutaneous Dehydroepiandrosterone Replacement Therapy in Postmenopausal Women.pdf

This study’s results show the beneficial effects of DHEA therapy in postmenopausal women without any significant side effects.  Fifteen postmenopausal women were studied for twelve months.
Diamond, P., Cusan, L., Gomez, J.L., Belanger, A. & Labrie, F. (1996). Metabolic effects of 12-month percutaneous dehydroepiandrosterone replacement therapy in postmenopausal women [Electronic version]. The Journal of Endocrinology, 150, Suppl. S43-50. Retrieved May 18, 2005.

Estrogen Replacement Therapy in Older Women: A Neuropsychological and Brain MRI Study.pdf

This study demonstrates an association between estrogen replacement therapy and better cognitive functioning and a lower rate of clinically unsuspected ischemic brain damage in postmenopausal women.
Schmidt, R., Fazekas, F., Reinhart, B., Kapeller, P., Fazekas, G., Offenbacher, H., et al. (1996). Estrogen replacement therapy in older women: a neuropsychological and brain MRI study [Electronic version]. Journal of the American Geriatric Society, 44(11), 1307-1313. Retrieved October 3, 2005.

Effect of Oestrogen During Menopause on Risk and Age at Onset of Alzheimer's Disease.pdf

The interpretation of this study is that oestrogen use in postmenopausal women may delay the onset and decrease the risk of Alzheimer's disease. Prospective studies are needed to establish the dose and duration of oestrogen required to provide this benefit and to assess its safety in elderly postmenopausal women.
Tang, M.X., Jacobs, D., Stern, Y., Marder, K., Schofield, P., Gurland, B., et al. (1996). Effect of oestrogen during menopause on risk and age at onset of Alzheimer's disease [Electronic version]. Lancet, 348(9025), 429-432. Retrieved October 3, 2005.

Effect of Hormone Replacement Therapy for Menopause on the Mechanical Properties of Skin.pdf

This study of 114 healthy women, including non-menopausal and menopausal with and without HRT, evaluated the effect of hormone replacement therapy for menopause on the mechanical properties of the skin.  It concluded beneficial effects on some of the properties.
Pierard, G.E., Letawe, C., Dowlati, A. & Pierard-Franchimont, C. (1995). Effect of hormone replacement therapy for menopause on the mechanical properties of skin [Electronic version]. Journal of the American Geriatrics Society, 43(6), 662-665. Retrieved May 18, 2005.

Skin Water-Holding Capacity and Transdermal Estrogen Therapy for Menopause: A Pilot Study.pdf

This study included two groups of fifteen menopausal women.  The purpose was to model and measure the influence of estrogen-transdermal HRT on subtle physiological changes taking place in the epidermis during perimenopause.
Pierard-Franchimont, C., Letawe, C., Goffin, V., Pierard, G.E. (1995). Skin water-holding capacity and transdermal estrogen therapy for menopause: a pilot study [Electronic version]. Maturitas, 22(2), 151-154. Retrieved May 18, 2005.

Evidence of a Healthy Estrogen User Survivor Effect.pdf

This article examined the relation between menopausal estrogen use and all-cause and cause-specific mortality in a cohort of over 49,000 women followed between 1979 and 1989 in the Breast Cancer Detection Demonstration Project (BCDDP) Follow-Up Study.

Sturgeon, S.R., Schairer, C., Brinton, L.A., Pearson, T., & Hoover, R.N. (1995). Evidence of a healthy estrogen user survivor effect [Electronic version]. Epidemiology, 6(3), 227-231. Retrieved October 3, 2005.

Comparison of Oral Estrogens and Estrogens Plus Androgen on Bone Mineral Density, Menopausal Symptoms, and Lipid-Lipoprotein Profiles in Surgical Menopause.pdf

This study concludes that oral estrogen-androgen increased vertebral bone mineral density compared with pre-treatment values and relieved somatic symptoms. Safety indices, including lipoprotein levels, indicated that the combination was well tolerated over the 2 years of treatment.
Watts, N.B., Notelovitz, M., Timmons, M.C., Addison, W.A., Wiita, B. & Downey, L.J. (1995). Comparison of oral estrogens and estrogens plus androgen on bone mineral density, menopausal symptoms, and lipid-lipoprotein profiles in surgical menopause [Electronic version]. Obstetrics and Gynecology, 85(4), 529-537. Retrieved October 3, 2005.

A Randomized, Double-Blind, Placebo-Controlled Study on the Effect of Conjugated Estrogens on Skin Thickness.pdf

This twelve-month study examines the possible increase in skin thickness in postmenopausal women as a result of being treated with conjugated estrogens.  The results of the study may be beneficial to women who are looking for information regarding the benefits of estrogen replacement therapy.
Maheux, R., Naud, F., Rioux, M., Grenier, R., Lemay, A., Guy, J. & Langevin, M. (1994). A randomized, double-blind, placebo-controlled study on the effect of conjugated estrogens on skin thickness [Electronic version]. American Journal of Obstetrics and Gynecology, 170(2), 642-649. Retrieved May 18, 2005.

Sex Hormones and Psychological Functioning in Postmenopausal Women.pdf

According to this paper, women who seek medical care around the time of menopause frequently report changes in one or more aspects of psychological functioning. The etiology of these symptoms is likely multifactorial and, undoubtedly, individual and sociocultural factors are important determinants.
Sherwin, B.B. (1994). Sex hormones and psychological functioning in postmenopausal women [Electronic version]. Experimental Gerontology, 29(3-4), 423-430. Retrieved October 3, 2005.

Increase in Bone Mass After One Year of Percutaneous Oestradiol and Testosterone Implants in Post-Menopausal Women Who Have Previously Received Long-Term Oral Oestrogens.pdf

This study concluded that subcutaneous oestradiol and testosterone implants will result in an increase in bone mass even after many years of oral oestrogen replacement therapy.
Savvas, M., Studd, J.W., Norman, S., Leather, A.T., Garnett, T.J. & Fogelman, I. (1992). Increase in bone mass after one year of percutaneous oestradiol and testosterone implants in post-menopausal women who have previously received long-term oral oestrogens [Electronic version]. British Journal of Obstetrics and Gynaecology, 99(9), 757-760. Retrieved October 3, 2005.

Sex Hormones and Skin Collagen Content in Postmenopausal Women.pdf

The implication from the findings in this study is that oestrogen or testosterone, or both, prevents the decrease in skin collagen content during the aging process.  It concludes that it protects skin in the same way as it protects bone in menopausal women.  Skin biopsy specimens were taken from the participants.
Brincat, M., Moniz, C.F., Studd, J.W., Darby, A.J., Magos, A. & Cooper, D. (1983). Sex hormones and skin collagen content in postmenopausal women [Electronic version]. British Medical Journal, 287(6402), 1337-1338. Retrieved May 18, 2005.