Serum adiponectin and coronary heart disease risk in older Black and White Americans

被引:58
|
作者
Kanaya, Alka M.
Fyr, Christina Wassel
Vittinghoff, Eric
Havel, Peter J.
Cesari, Matteo
Nicklas, Barbara
Harris, Tamara
Newman, Anne B.
Satterfield, Suzanne
Cummings, Steve R.
机构
[1] Univ Calif San Francisco, San Francisco, CA 94115 USA
[2] Univ Calif Davis, Davis, CA 95616 USA
[3] Univ Florida, Dept Aging & Geriatr Res, Gainesville, FL 32611 USA
[4] Wake Forest Univ, Med Ctr, Winston Salem, NC 27157 USA
[5] Intramural Res Program, NIH, Bethesda, MD 20892 USA
[6] Univ Tennessee, Knoxville, TN 37996 USA
[7] Univ Pittsburgh, Pittsburgh, PA 15260 USA
[8] Calif Pacific Med Ctr, San Francisco, CA 94118 USA
来源
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 2006年 / 91卷 / 12期
关键词
D O I
10.1210/jc.2006-0107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Adiponectin may influence the risk of coronary heart disease (CHD) independently of traditional cardiovascular risk factors. Objective: Because body composition and adiponectin levels vary by race, we examined the relationship of adiponectin with prevalent and incident CHD in a cohort of older Black and White adults. Design and Setting: We conducted a cross-sectional and prospective cohort study at two U. S. clinical centers. Participants: Participants included 3075 well-functioning adults between ages 70 and 79 yr enrolled in the Health, Aging, and Body Composition study. Main Outcome Measures: Prevalent CHD was defined as history of myocardial infarction, coronary artery bypass graft, percutaneous coronary transluminal angioplasty, angina, or major electrocardiogram abnormalities. After excluding those with prevalent CHD, incident CHD was defined as hospitalized myocardial infarction or CHD death. Results: At baseline, 602 participants (19.6%) had CHD. During 6 yr of follow-up, 262 (10.6%) incident CHD events occurred. Whites had higher median adiponectin than Blacks (12 vs. 8 mu g/ml, P < 0.001). Race modified the effect of adiponectin (P for interaction was 0.002 for prevalent CHD, and P = 0.02 for incident CHD). Among Whites, an inverse association of adiponectin with CHD was explained by high-density lipoprotein and glucose. Among Blacks, a doubling of adiponectin was associated with a 40% higher risk of both prevalent CHD (odds ratio, 1.41; 95% confidence interval, 1.11-1.78) and incident CHD (hazards ratio, 1.37; 95% confidence interval, 1.01-1.87) after adjusting for explanatory variables. Conclusion: High circulating concentrations of adiponectin were associated with higher risk of CHD in older Blacks, even accounting for traditional CHD risk factors.
引用
收藏
页码:5044 / 5050
页数:7
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