Cardiovascular risk prediction in people with chronic kidney disease

被引:35
|
作者
Matsushita, Kunihiro [1 ,2 ]
Ballew, Shoshana H. [1 ,2 ]
Coresh, Josef [1 ,2 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, 2024 E Monument St,Suite 2-600, Baltimore, MD 21287 USA
[2] Welch Ctr Prevent Epidemiol & Clin Res, 2024 E Monument St,Suite 2-600, Baltimore, MD 21287 USA
来源
关键词
albuminuria; cardiovascular disease; estimated glomerular filtration rate; risk prediction; GLOMERULAR-FILTRATION-RATE; CORONARY-HEART-DISEASE; ATHEROSCLEROSIS RISK; CYSTATIN C; COLLABORATIVE METAANALYSIS; ALL-CAUSE; ALBUMINURIA; MORTALITY; ASSOCIATION; OUTCOMES;
D O I
10.1097/MNH.0000000000000265
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewClinical guidelines are not consistent regarding whether or how to utilize information on measures of chronic kidney disease (CKD) for predicting the risk of cardiovascular disease (CVD). This review summarizes recent literature regarding CVD prediction in the context of CKD.Recent findingsPrevious studies used different definitions of CKD measures and CVD outcomes, and applied distinct statistical approaches. A recent individual-level meta-analysis from the CKD Prognosis Consortium is of value as it has uniformly investigated creatinine-based estimated glomerular filtration rate (eGFR) and albuminuria as CKD measures and applied the same statistical approach across 24 cohorts with more than 630000 participants. In this meta-analysis, eGFR and albuminuria improve CVD risk prediction beyond traditional CVD risk factors, particularly for CVD mortality and heart failure. Albuminuria demonstrates more evident improvement than eGFR. Moreover, several recent studies have shown that other filtration markers, for example, cystatin C and (2)-microglobulin, and measures of atherosclerosis or cardiac damage (e.g., coronary artery calcium and cardiac troponins) can further improve CVD prediction in the CKD population.SummaryFuture clinical guidelines may require updates regarding whether/how to incorporate CKD measures and other biomarkers in CVD prediction, depending on the CVD outcomes of interest, target population, and availability of those measures/biomarkers in that population.
引用
收藏
页码:518 / 523
页数:6
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