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Issue 1052 coverThe Future of Hormone Therapy: What Basic Science and Clinical Studies Teach Us Volume 1052 published June 2005
Ann. N.Y. Acad. Sci. 1052: 43–56 (2005). doi: 10.1196/annals.1347.004
Copyright © 2005 by the New York Academy of Sciences
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Articles by HARMAN, S M.
Articles by JUDELSON, D. R.
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Articles by HARMAN, S M.
Articles by JUDELSON, D. R.
Is the Estrogen Controversy Over? Deconstructing the Women's Health Initiative Study: A Critical Evaluation of the Evidence

S MITCHELL HARMANa, FREDERICK NAFTOLINb, ELIOT A. BRINTONc AND DEBRA R. JUDELSONd

aKronos Longevity Research Institute, Phoenix, Arizona 85016, USA
bYale University College of Medicine, New Haven, Connecticut 06511, USA
cUniversity of Utah School of Medicine, Salt Lake City, Utah 84112, USA
dWomen's Heart Institute, Cardiovascular Medical Group of Southern California, Beverly Hills, California 90210, USA

Address for correspondence: S. Mitchell Harman, M.D., Ph.D., Kronos Longevity Research Institute, 2222 E. Highland, Ste. 220, Phoenix, AZ 85016. Voice: 602-778-7484; fax: 602-778-7485. mitch.harman{at}kronosinstitute.org

The Women's Health Initiative (WHI) hormone trials have been widely interpreted as demonstrating that combined menopausal hormone therapy (HT) fails to protect against—and may increase—cardiovascular disease (CVD), stroke, and dementia in menopausal women, regardless of whether initiated early in the menopause or later. This conclusion does not agree with results of large epidemiological studies showing protection by HT and by estrogen replacement alone (ET) against CVD and dementia. One possible reason for this inconsistency is that the epidemiologic data are confounded by "healthy user bias." Another possible explanation is that most women in the observational studies initiated ET or HT at or near the menopausal transition, at which point there is little or no arterial injury, whereas, in the WHI studies, older women, averaging approximately 12 years postmenopausal, many of whom would have had significant asymptomatic atherosclerosis, were treated. Substantial data demonstrate atheropreventive effects of estrogen before vascular damage occurs, whereas adverse effects of oral estrogen on thrombosis and inflammation may predominate once complex atheromas are present. Similarly, the excess of dementia observed in older WHI women treated with oral conjugated estrogen could be due to cerebral thromboses (multi-infarct dementia). Given the uncertain relevance of the WHI (and other published randomized clinical trials) to initiation of HT in perimenopausal women, and its subsequent continuation for atheroprevention, new trials will be needed to resolve whether early intervention with estrogen may prevent CVD and/or dementia. The Kronos Early Estrogen Prevention Study (KEEPS), which began in mid-2005, is a randomized, controlled multicenter trial of HT in recently menopausal women. It will examine surrogate end points as well as risk factors for atherosclerosis.

Key Words: menopause • estrogen • hormone therapy • atherosclerosis • cardiovascular disease • dementia




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