The Association of Chronic Kidney Disease andMetabolic Syndrome with Incident Cardiovascular Events: Multiethnic Study of Atherosclerosis

被引:13
作者
Agarwal, Subhashish [1 ]
Shlipak, Michael G. [2 ,3 ]
Kramer, Holly [4 ,5 ]
Jain, Aditya [6 ]
Herrington, David M. [1 ]
机构
[1] Wake Forest Sch Med, Cardiol Sect, Winston Salem, NC 27157 USA
[2] San Francisco VA Med Ctr, Gen Internal Med Div, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
[4] Loyola Univ, Med Ctr, Dept Prevent Med, Maywood, IL 60153 USA
[5] Loyola Univ, Med Ctr, Div Nephrol & Hypertens, Maywood, IL 60153 USA
[6] Johns Hopkins Univ, Dept Radiol, Baltimore, MD 21205 USA
关键词
D O I
10.1155/2012/806102
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. There is an association between chronic kidney disease (CKD) and metabolic syndrome (MetS). We examined the joint association of CKD and MetS with incident cardiovascular (CVD) events in the Multiethnic Study of Atherosclerosis (MESA) cohort. Methods. We analyzed 2,283 Caucasians, 363 Chinese, 1,449 African-Americans, and 1,068 Hispanics in the MESA cohort. CKD was defined by cystatin C estimated glomerular filtration rate <= 60 mL/min/1.73m(2) and MetS was defined by NCEP criteria. Cox proportional regression adjusting for age, ethnicity, gender, study site, education, income, smoking, alcohol use, physical activity, and total and LDL cholesterol was performed to assess the joint association of CKD and MetS with incident CVD events. Participants were divided into four groups by presence of CKD and/or MetS and compared to the group without CKD and MetS (CKD-/MetS-). Tests for additive and multiplicative interactions between CKD and MetS and prediction of incident CVD were performed. Results. During follow-up period of 5.5 years, 283 participants developed CVD. Multivariate Cox regression analysis demonstrated that CKD and MetS were independent predictors of CVD (hazard ratio, 2.02 for CKD, and 2.55 for MetS). When participants were compared to the CKD-/MetS- group, adjusted HR for the CKD+/MetS(+) group was 5.56 (95% CI 3.72-8.12). There was no multiplicative interaction between CKD and MetS (P = 0.2); however, there was presence of additive interaction. The relative excess risk for additive interaction (RERI) was 2.73, P = 0.2, and the attributable portion (AP) was 0.49 (0.24-0.74). Conclusion. Our findings illustrate that the combination of CKD and MetS is a strong predictor of incident clinical cardiovascular events due to presence of additive interaction between CKD and MetS.
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页数:8
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