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PMID: 12771114 Published · ppublish English Clinical Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, U.S. Gov't, P.H.S.

Effect of estrogen plus progestin on stroke in postmenopausal women: the Women's Health Initiative: a randomized trial.

JAMA ·Vol. 289 ·No. 20 ·2003-05-28 ·Pages 2673-84

Wassertheil-Smoller S, Hendrix SL, Limacher M, Heiss G, Kooperberg C, Baird A, Kotchen T, Curb JD, Black H, Rossouw JE, Aragaki A, Safford M, Stein E, Laowattana S, Mysiw WJ, WHI Investigators

Abstract

The Women's Health Initiative (WHI) trial of estrogen plus progestin was stopped early because of adverse effects, including an increased risk of stroke in the estrogen plus progestin group. To assess the effect of estrogen plus progestin on ischemic and hemorrhagic stroke and in subgroups, and to determine whether the effect of estrogen plus progestin was modified by baseline levels of blood biomarkers. Multicenter double-blind, placebo-controlled, randomized clinical trial involving 16 608 women aged 50 through 79 years with an average follow-up of 5.6 years. Baseline levels of blood-based markers of inflammation, thrombosis, and lipid levels were measured in the first 140 centrally confirmed stroke cases and 513 controls. Participants received 0.625 mg/d of conjugated equine estrogen plus 2.5 mg/d of medroxyprogesterone acetate (n = 8506) or placebo (n = 8102). Overall strokes and stroke subtype and severity were centrally adjudicated by stroke neurologists. One hundred fifty-one patients (1.8%) in the estrogen plus progestin and 107 (1.3%) in the placebo groups had strokes. Overall 79.8% of strokes were ischemic. For combined ischemic and hemorrhagic strokes, the intention-to-treat hazard ratio (HR) for estrogen plus progestin vs placebo was 1.31 (95% confidence interval [CI], 1.02-1.68); with adjustment for adherence, the HR was 1.50 (95% CI, 1.08-2.08). The HR for ischemic stroke was 1.44 (95% CI, 1.09-1.90) and for hemorrhagic stroke, 0.82 (95% CI, 0.43-1.56). Point estimates of the HRs indicate that excess risk of all stroke was apparent in all age groups, in all categories of baseline stroke risk, and in women with and without hypertension, prior history of cardiovascular disease, use of hormones, statins, or aspirin. Other risk factors for stroke, including smoking, blood pressure, diabetes, lower use of vitamin C supplements, blood-based biomarkers of inflammation, higher white blood cell count, and higher hematocrit levels did not modify the effect of estrogen plus progestin on stroke risk. Estrogen plus progestin increases the risk of ischemic stroke in generally healthy postmenopausal women. Excess risk for all strokes attributed to estrogen plus progestin appeared to be present in all subgroups of women examined.

MeSH Terms
Aged Biomarkers/blood Double-Blind Method Estrogen Replacement Therapy/adverse effects Estrogens, Conjugated (USP)/adverse effects,therapeutic use Female Humans Medroxyprogesterone Acetate/adverse effects,therapeutic use Middle Aged Postmenopause Progesterone Congeners/adverse effects,therapeutic use Proportional Hazards Models Risk Factors Stroke/chemically induced,classification,epidemiology Survival Analysis
Chemicals
Biomarkers Estrogens, Conjugated (USP) Progesterone Congeners Medroxyprogesterone Acetate
Authors & Affiliations
16 authors, click to expand affiliations / ORCID
Wassertheil-Smoller Sylvia
Department of Epidemiology and Social Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA. [email protected]
Hendrix Susan L
Limacher Marian
Heiss Gerardo
Kooperberg Charles
Baird Alison
Kotchen Theodore
Curb J David
Black Henry
Rossouw Jacques E
Aragaki Aaron
Safford Monika
Stein Evan
Laowattana Somchai
Mysiw W Jerry
WHI Investigators
Article Info
Journal
JAMA
Abbr.
JAMA
ISSN
0098-7484
Published
2003-05-28
Pages
2673-84
Language
English
Region
United States
NLM ID
7501160
Subset
IM
Corrections
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