Lipid changes on hormone therapy and coronary heart disease events in the Heart and Estrogen/progestin Replacement Study (HERS) - 28/08/11
, Lily A Chaput, MD, MPH c, Eric Vittinghoff, PhD c, Feng Lin, MS c, Vera Bittner, MD d, Robert H Knopp, MD e, Stephen B Hulley, MD, MPH cHeart and Estrogen/progestin Replacement Study (HERS) Investigators
Abstract |
Background |
Despite the effect of lowering low-density lipoprotein cholesterol (LDL-C) levels and raising high-density lipoprotein cholesterol (HDL-C) levels, combination hormone therapy did not reduce the incidence of coronary heart disease (CHD) events in the Heart and Estrogen/progestin Replacement Study (HERS). To explore possible mechanisms, we examined the association between lipid changes and CHD outcomes among women assigned to hormone therapy.
Methods |
HERS participants were postmenopausal women with previously diagnosed CHD who were randomly assigned to receive conjugated estrogens and medroxyprogesterone or identical placebo and then followed-up for an average of 4.1 years. Among women assigned to hormone therapy, associations between baseline-to-year-1 lipid level changes and CHD events were compared with the associations observed for baseline lipids using multivariate proportional hazards models.
Results |
Among women assigned to hormone therapy, CHD events were independently predicted by baseline LDL-C levels (relative hazard [RH] 0.94 per 15.6 mg/dL decrease, 95% CI 0.88–1.01) and HDL-C levels (RH 0.89 per 5.4 mg/dL increase, 95% CI 0.81–0.99), but not by triglyceride levels (RH 1.01 per 13.2mg/dL increase, 95% CI 0.97–1.06). CHD events were marginally associated with first-year reductions in LDL-C levels (RH 0.95 per 15.6mg/dL decrease, 95% CI 0.86–1.04), and were not associated with increases in HDL-C levels ( RH 1.03 per 5.4 mg/dL increase, 95% CI 0.91–1.16) or triglyceride levels (RH 1.01 per 13.2 mg/dL increase, 95% CI 0.98–1.05).
Conclusion |
Changes in lipid levels with hormone therapy are not predictive of CHD outcomes in women with heart disease in the HERS trial.
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| HERS was supported by a contract with Wyeth-Ayerst Research (Radnor, Pa). Dr. Shlipak is a recipient of a Research Career Development Award from the Veterans Administration division of Health Services Research and Development. |
Vol 146 - N° 5
P. 870-875 - novembre 2003 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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