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Vasan RS, Beiser A, D'Agostino RB, et al. Plasma Homocysteine and Risk for Congestive Heart Failure in Adults Without Prior Myocardial Infarction. JAMA. 2003;289(10):1251–1257. doi:10.1001/jama.289.10.1251
Author Affiliations: National Heart, Lung, and Blood Institute's Framingham Heart Study (Drs Vasan, Beiser, D' Agostino, Levy, and Wilson), Framingham, Mass; Cardiology Section (Dr Vasan), Endocrinology Section (Dr Wilson), Preventive Medicine and Epidemiology (Drs Vasan, Levy, and Wilson), Department of Medicine, Boston University School of Medicine, and Department of Biostatistics, Boston University School of Public Health (Dr Beiser); and Department of Mathematics (Dr D'Agostino), Boston University, Boston, Mass; the Divisions of Cardiology and Clinical Epidemiology, Beth Israel Deaconess Medical Center (Dr Levy), Boston, Mass; and the National Heart, Lung, and Blood Institute, Bethesda, Md (Dr Levy); the Jean Mayer US Department of Agriculture Human Nutrition Research Center on Aging (Drs Selhub, Jacques, and Rosenberg) at Tufts University, Boston, Mass.
Context Elevated plasma homocysteine levels are associated with increased risk
of vascular disease. It is unclear whether elevated homocysteine levels are
a risk factor for congestive heart failure (CHF).
Objective To study prospectively the association between nonfasting plasma homocysteine
and incidence of CHF.
Design, Setting, and Participants Community-based prospective cohort study of 2491 adults (mean age 72
years, 1547 women) who participated in the Framingham Heart Study during the
1979-1982 and 1986-1990 examinations and were free of CHF or prior myocardial
infarction (recognized or unrecognized) at baseline.
Main Outcome Measure Incidence of a first episode of CHF during an 8-year follow-up period.
Results During follow-up, 156 subjects (88 women) developed CHF. In multivariable
analyses controlling for established risk factors for CHF including the occurrence
of myocardial infarction (recognized or unrecognized) during follow-up, plasma
homocysteine levels higher than the sex-specific median value were associated
with an adjusted hazards ratio for heart failure of 1.93 in women (95% confidence
interval, 1.19-3.14) and 1.84 in men (95% confidence interval, 1.06-3.17).
The relation of plasma homocysteine levels to CHF risk was more continuous
in women than in men. In analyses restricted to participants without any manifestation
of coronary heart disease at baseline, the association of plasma homocysteine
levels with risk of CHF was maintained in men and women.
Conclusions An increased plasma homocysteine level independently predicts risk of
the development of CHF in adults without prior myocardial infarction. Additional
investigations are warranted to confirm these findings.
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