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Postmenopausal hormone therapy: critical reappraisal and a unified hypothesis.
Fertil Steril. 2005 Mar; 83(3):558-66.FS

Abstract

OBJECTIVE

To reconcile apparently conflicting evidence regarding the use of hormone therapy as a health-preserving strategy in postmenopausal women in light of that fact that findings from animal studies, human observation studies, and human clinical trials are consistent for outcomes such as fracture and breast cancer but differ for coronary heart disease (CHD).

DESIGN

Literature review and generation of a unified hypothesis consistent with all of the data.

SETTING

Animal trials, human observational studies, human studies of biologic intermediates, and human clinical trials.

PATIENT(S)

Premenopausal and postmenopausal women with or without antecedent CHD.

MAIN OUTCOME MEASURE(S)

Coronary heart disease events, proxies, risk factors, and related mechanisms.

RESULT(S)

The complex CHD responses to hormone therapy in recent human trials likely reflect a combination of [1] early erosion/rupture of "vulnerable" coronary plaque, which is made worse by hormone therapy, [2] long-term reduction in plaque formation, which is improved by hormone therapy, and [3] modulation of the vasculoprotective actions of estrogens by systemic progestogens.

CONCLUSION(S)

The unified hypothesis predicts that hormone therapy initiated at the time of menopause should produce a decrease in CHD over time. In contrast, hormone therapy begun years after menopause should produce an increase in CHD events shortly after therapy is begun, followed later by benefit. In women who require progestogens for endometrial protection, there should be greater CHD benefit from use of progestogens with less systemic activity. The unified hypothesis is consistent both with plausible biologic mechanisms and with evidence from animal studies, human observational studies, and human clinical trials such as the Women's Health Initiative. In the absence of evidence from human trials that specifically involve initiation of hormone therapy in perimenopausal women, practitioners and patients can use the unified hypothesis as a rational tool to guide decisions about clinical management.

Authors+Show Affiliations

General Clinical Research Center, Emory University Hospital, Division of Endocrinology and Metabolism, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA. medlsp@emory.eduNo affiliation info available

Pub Type(s)

Journal Article
Research Support, U.S. Gov't, P.H.S.
Review

Language

eng

PubMed ID

15749481

Citation

Phillips, Lawrence S., and Robert D. Langer. "Postmenopausal Hormone Therapy: Critical Reappraisal and a Unified Hypothesis." Fertility and Sterility, vol. 83, no. 3, 2005, pp. 558-66.
Phillips LS, Langer RD. Postmenopausal hormone therapy: critical reappraisal and a unified hypothesis. Fertil Steril. 2005;83(3):558-66.
Phillips, L. S., & Langer, R. D. (2005). Postmenopausal hormone therapy: critical reappraisal and a unified hypothesis. Fertility and Sterility, 83(3), 558-66.
Phillips LS, Langer RD. Postmenopausal Hormone Therapy: Critical Reappraisal and a Unified Hypothesis. Fertil Steril. 2005;83(3):558-66. PubMed PMID: 15749481.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Postmenopausal hormone therapy: critical reappraisal and a unified hypothesis. AU - Phillips,Lawrence S, AU - Langer,Robert D, PY - 2004/04/22/received PY - 2004/11/09/revised PY - 2004/11/09/accepted PY - 2005/3/8/pubmed PY - 2005/5/6/medline PY - 2005/3/8/entrez SP - 558 EP - 66 JF - Fertility and sterility JO - Fertil Steril VL - 83 IS - 3 N2 - OBJECTIVE: To reconcile apparently conflicting evidence regarding the use of hormone therapy as a health-preserving strategy in postmenopausal women in light of that fact that findings from animal studies, human observation studies, and human clinical trials are consistent for outcomes such as fracture and breast cancer but differ for coronary heart disease (CHD). DESIGN: Literature review and generation of a unified hypothesis consistent with all of the data. SETTING: Animal trials, human observational studies, human studies of biologic intermediates, and human clinical trials. PATIENT(S): Premenopausal and postmenopausal women with or without antecedent CHD. MAIN OUTCOME MEASURE(S): Coronary heart disease events, proxies, risk factors, and related mechanisms. RESULT(S): The complex CHD responses to hormone therapy in recent human trials likely reflect a combination of [1] early erosion/rupture of "vulnerable" coronary plaque, which is made worse by hormone therapy, [2] long-term reduction in plaque formation, which is improved by hormone therapy, and [3] modulation of the vasculoprotective actions of estrogens by systemic progestogens. CONCLUSION(S): The unified hypothesis predicts that hormone therapy initiated at the time of menopause should produce a decrease in CHD over time. In contrast, hormone therapy begun years after menopause should produce an increase in CHD events shortly after therapy is begun, followed later by benefit. In women who require progestogens for endometrial protection, there should be greater CHD benefit from use of progestogens with less systemic activity. The unified hypothesis is consistent both with plausible biologic mechanisms and with evidence from animal studies, human observational studies, and human clinical trials such as the Women's Health Initiative. In the absence of evidence from human trials that specifically involve initiation of hormone therapy in perimenopausal women, practitioners and patients can use the unified hypothesis as a rational tool to guide decisions about clinical management. SN - 0015-0282 UR - https://www.unboundmedicine.com/medline/citation/15749481/Postmenopausal_hormone_therapy:_critical_reappraisal_and_a_unified_hypothesis_ DB - PRIME DP - Unbound Medicine ER -