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Conference 2005

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ANDROGENS AND ESTROGENS IN WOMEN: RESTORING THE BALANCE

Vliet, E.L.

Founder, HER Place: Health Enhancement and Renewal for Women, Inc. Dallas, TX and P.O. Box 64507, Tucson, AZ 85728, USA

Hormone therapy for menopause has been under attack since the publication of the Women's Health Initiative in the United States and the Million Women Study in the United Kingdom. Both studies have serious limitations, yet have been generalized to all ages of women needing hormones, all types and routes of delivery for hormones, in spite of decades of basic science studies in animal models and humans, pharmacological research, epidemiological and clinical studies that have shown marked differences in outcomes and risks with different types and routes of delivery. This presentation will briefly review some of the critical flaws of each study that limit applicability to all groups of women. Although the focus for approved indications for hormone therapy at menopause has been elimination of vasomotor symptoms, atrophic vaginitis, and prevention of bone loss, a wealth of basic science and clinical research over the last five decades has demonstrated that ovarian gonadal hormones play multiple metabolic, endocrine, and neuroendocrine roles throughout the body. Loss of these critical hormones at menopause sets the stage for increased risk of metabolic syndrome and diabetes, cardiovascular disorders, cognitive decline, immune dysfunction, loss of muscle mass, adverse changes in joints and connective tissue, among other effects. This presentation will review key areas of research that show such multiple effects of ovarian hormones in women. This presentation will also discuss the ways that different types of estrogen options for hormone therapy have an impact on crucial androgen balance in women. For example, oral conjugated equine estrogens (e.g. Premarin, Prempro) have long been known to increase sex hormone binding globulin (SHBG) and decrease the free fraction of testosterone and estradiol. Non-oral delivery systems can eliminate most of the hepatic first pass effect on increased SHBG production. Androgens, in balance with optimal estradiol, play a critical role in women to maintain lean body mass and reduce the progressive tendency for postmenopausal women to gain fat mass as they age. Progestins have been used for menopausal hormone therapy primarily to reduce the risk of hyperplasia and endometrial carcinoma from unopposed estrogen in women with an intact uterus. Newer studies, clinical and basic science, suggest that various types of progestins have quite different risk profiles and ability to attenuate the documented benefits of both androgens and estrogens. For example, medroxyprogesterone acetate has been shown to accelerate the clumping of abnormal proteins in the CNS that lead to development of Alzheimer's, but this effect was not seen with the progestin norethisterone or the natural ovarian progestagen, progesterone. Data will be presented to illustrate these important differences in progestins, as well as the impact of various types of estrogens on androgen balance. This presentation will primarily focus on the clinical relevance of this wealth of research and discuss practical approaches for the clinician in assessing women and developing hormone therapy approaches tailored to the individual woman's health risks, clinical history, biomedical markers, and personal preferences and health goals. There will also be case vignettes of the differences in objective markers and subjective patient responses to various preparations of estrogens, progestins, and androgens.