Issues to debate on the Women's Health Initiative (WHI) study - Hormone replacement therapy and acute coronary outcomes: methodological issues between randomized and observational studies

被引:57
作者
Garbe, E
Suissa, S [1 ]
机构
[1] McGill Univ, Royal Victoria Hosp, Dept Epidemiol & Biostat, Div Clin Epidemiol,Pharmacoepidemiol Res Unit, Montreal, PQ H3A 1A1, Canada
[2] Humboldt Univ, Charite, Inst Clin Pharmacol, D-10117 Berlin, Germany
[3] Inst Pharmacoepidemiol & Technol Assessment, D-10117 Berlin, Germany
基金
加拿大健康研究院;
关键词
acute myocardial infarction; detection bias; healthy user bias; observational studies; Women's Health Initiative study;
D O I
10.1093/humrep/deh022
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
A large number of observational studies, supported by animal and basic research studies, have shown a protective effect of hormone replacement therapy (HRT) on acute coronary outcomes. The recent large randomized Women's Health Initiative (WHI) study reported the opposite result, i.e. a small risk increase of 29% for acute coronary outcomes under estrogen-progestin treatment. Possible methodological reasons for these discrepancies are discussed. Despite randomization, the reported small increase in risk in the WHI study could be spurious because of differential unblinding of HRT users, which could have resulted in higher detection rates of otherwise clinically unrecognized acute myocardial infarction in these women. We show that altering diagnostic patterns because of unblinding could lower the crude rate ratio of 1.28 to 1.02. In the observational studies, the protective effect may have been exaggerated due to a healthy user bias and to the inappropriate choice of the reference group. Using an alternative reference group, the combined rate ratio of 0.67 was increased to 0.82. The diametrical effects of HRT on acute coronary outcomes found between the observational studies and the WHI Study may be a result not only of bias in the observational studies, but also of bias in the WHI Study.
引用
收藏
页码:8 / 13
页数:6
相关论文
共 40 条
[1]   INHIBITION OF CORONARY-ARTERY ATHEROSCLEROSIS BY 17-BETA ESTRADIOL IN OVARIECTOMIZED MONKEYS - LACK OF AN EFFECT OF ADDED PROGESTERONE [J].
ADAMS, MR ;
KAPLAN, JR ;
MANUCK, SB ;
KORITNIK, DR ;
PARKS, JS ;
WOLFE, MS ;
CLARKSON, TB .
ARTERIOSCLEROSIS, 1990, 10 (06) :1051-1057
[2]   Estrogens inhibit angiotensin II-induced leukocyte-endothelial cell interactions in vivo via rapid endothelial nitric oxide synthase and cyclooxygenase activation [J].
Alvarez, A ;
Hermenegildo, C ;
Issekutz, AC ;
Esplugues, JV ;
Sanz, MJ .
CIRCULATION RESEARCH, 2002, 91 (12) :1142-1150
[3]   Hormone replacement therapy, heart disease, and other considerations [J].
Barrett-Connor, E ;
Grady, D .
ANNUAL REVIEW OF PUBLIC HEALTH, 1998, 19 :55-72
[4]   A comparison of observational studies and randomized, controlled trials. [J].
Benson, K ;
Hartz, AJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (25) :1878-1886
[5]  
CANNER PL, 1980, NEW ENGL J MED, V303, P1038
[6]  
Clarkson TB, 1996, BRIT J OBSTET GYNAEC, V103, P53
[7]   Randomized, controlled trials, observational studies, and the hierarchy of research designs. [J].
Concato, J ;
Shah, N ;
Horwitz, RI .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (25) :1887-1892
[8]  
Genazzani AR, 2002, GYNECOL ENDOCRINOL, V16, P255
[9]   HORMONE-THERAPY TO PREVENT DISEASE AND PROLONG LIFE IN POSTMENOPAUSAL WOMEN [J].
GRADY, D ;
RUBIN, SM ;
PETITTI, DB ;
FOX, CS ;
BLACK, D ;
ETTINGER, B ;
ERNSTER, VL ;
CUMMINGS, SR .
ANNALS OF INTERNAL MEDICINE, 1992, 117 (12) :1016-1037
[10]   Understanding the divergent data on postmenopausal hormone therapy [J].
Grodstein, F ;
Clarkson, TB ;
Manson, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :645-650