Filtration Markers as Predictors of ESRD and Mortality: Individual Participant Data Meta-Analysis

被引:23
作者
Inker, Lesley A. [1 ]
Coresh, Josef [2 ]
Sang, Yingying [2 ]
Hsu, Chi-Yuan [3 ]
Foster, Meredith C. [1 ]
Eckfeldt, John H. [4 ]
Karger, Amy B. [4 ]
Nelson, Robert G. [5 ]
Liu, Xun [1 ]
Sarnak, Mark [1 ]
Appel, Lawrence J. [2 ]
Grams, Morgan [2 ]
Xie, Dawei [6 ]
Kimmel, Paul L. [7 ]
Feldman, Harold [6 ]
Ramachandran, Vasan [8 ]
Levey, Andrew S. [1 ]
机构
[1] Tufts Med Ctr, William B Schwartz Div Nephrol, 800 Washington St,Box 391, Boston, MA 02111 USA
[2] Johns Hopkins Univ, Welch Ctr Prevent Epidemiol & Clin Res, Baltimore, MD USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[4] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[5] NIDDKD, NIH, Phoenix, AZ USA
[6] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[7] NIDDKD, NIH, Bethesda, MD USA
[8] Boston Univ, Sch Med, Boston, MA 02118 USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2017年 / 12卷 / 01期
基金
美国国家卫生研究院;
关键词
SERUM CYSTATIN-C; COLLABORATIVE METAANALYSIS; CARDIOVASCULAR MORTALITY; HIGHER ALBUMINURIA; KIDNEY-DISEASE; ALL-CAUSE; RISK; CREATININE;
D O I
10.2215/CJN.03660316
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
Background and objectives Serum beta-trace protein (BTP) and beta-2 microglobulin (B2M) are associated with risk of ESRD and death in the general population and in populations at high risk for these outcomes (GP/HR) and those with CKD, but results differ among studies. Design, setting, participants, & measurements We performed an individual patient-level meta-analysis including three GP/HR studies (n=17,903 participants) and three CKD studies (n=5415). We compared associations, risk prediction, and improvement in reclassification of eGFR using BTP (eGFR(BTP)) and B2M (eGFR(B2M)) alone and the average (eGFR(avg)) of eGFR(BTP), eGFR(B2M), creatinine (eGFR(cr)), and cystatin C (eGFR(cys)), to eGFR(cr), eGFR(cys), and their combination (eGFR(cr-cys)) for ESRD (2075 events) and death (7275 events). Results Mean (SD) follow up times for ESRD and mortality for GP/HR and CKD studies were 13 (4), 6.2 (3.2), 14 (5), and 7.5 (3.9) years, respectively. Compared with eGFR(cr), eGFR(BTP) and eGFR(B2M) improved risk associations and modestly improved prediction for ESRD and death even after adjustment for established risk factors. eGFRavg provided the most consistent improvement in associations and prediction across both outcomes and populations. Assessment of heterogeneity did not yield clinically relevant differences. For ESRD, addition of albuminuria substantially attenuated the improvement in risk prediction and risk classification with novel filtration markers. For mortality, addition of albuminuria did not affect the improvement in risk prediction with the use of novel markers, but lessened improvement in risk classification, especially for the CKD cohort. Conclusions These markers do not provide substantial additional prognostic information to eGFRcr and albuminuria, but may be appropriate in circumstances where eGFR(cr) is not accurate or albuminuria is not available. Educational efforts to increase measurement of albuminuria in clinical practice may be more cost-effective than measurement of BTP and B2M for improving prognostic information.
引用
收藏
页码:69 / 78
页数:10
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