Cystatin C versus Creatinine in Determining Risk Based on Kidney Function

被引:696
作者
Shlipak, Michael G. [1 ,2 ]
Matsushita, Kunihiro [3 ]
Arnlov, Johan [4 ,5 ]
Inker, Lesley A. [6 ]
Katz, Ronit [7 ]
Polkinghorne, Kevan R. [8 ,9 ]
Rothenbacher, Dietrich [10 ,11 ]
Sarnak, Mark J. [6 ]
Astor, Brad C. [12 ]
Coresh, Josef [3 ]
Levey, Andrew S. [6 ]
Gansevoort, Ron T. [13 ]
机构
[1] Univ Calif San Francisco, Div Gen Internal Med, San Francisco Vet Affairs Med Ctr, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med Epidemiol & Biostat, San Francisco, CA 94143 USA
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] Geriatr Uppsala Univ, Dept Publ Hlth & Caring Sci, Uppsala, Sweden
[5] Dalarna Univ, Sch Hlth & Social Studies, Falun, Sweden
[6] Tufts Med Ctr, Div Nephrol, Boston, MA USA
[7] Univ Washington, Seattle, WA 98195 USA
[8] Monash Univ, Dept Nephrol, Monash Med Ctr, Melbourne, Vic 3004, Australia
[9] Monash Univ, Dept Med, Melbourne, Vic, Australia
[10] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[11] Univ Ulm, Inst Epidemiol & Med Biometry, Ulm, Germany
[12] Univ Wisconsin, Dept Populat Hlth Sci, Sch Med & Publ Hlth, Madison, WI 53706 USA
[13] Univ Groningen, Univ Med Ctr Groningen, Dept Nephrol, Groningen, Netherlands
关键词
GLOMERULAR-FILTRATION-RATE; STAGE RENAL-DISEASE; COLLABORATIVE METAANALYSIS; HIGHER ALBUMINURIA; ESTIMATED GFR; ALL-CAUSE; HEART-FAILURE; CKD-EPI; MORTALITY; ASSOCIATION;
D O I
10.1056/NEJMoa1214234
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Adding the measurement of cystatin C to that of serum creatinine to determine the estimated glomerular filtration rate (eGFR) improves accuracy, but the effect on detection, staging, and risk classification of chronic kidney disease across diverse populations has not been determined. METHODS We performed a meta-analysis of 11 general-population studies (with 90,750 participants) and 5 studies of cohorts with chronic kidney disease (2960 participants) for whom standardized measurements of serum creatinine and cystatin C were available. We compared the association of the eGFR, as calculated by the measurement of creatinine or cystatin C alone or in combination with creatinine, with the rates of death (13,202 deaths in 15 cohorts), death from cardiovascular causes (3471 in 12 cohorts), and end-stage renal disease (1654 cases in 7 cohorts) and assessed improvement in reclassification with the use of cystatin C. RESULTS In the general-population cohorts, the prevalence of an eGFR of less than 60 ml per minute per 1.73 m(2) of body-surface area was higher with the cystatin C-based eGFR than with the creatinine-based eGFR (13.7% vs. 9.7%). Across all eGFR categories, the reclassification of the eGFR to a higher value with the measurement of cystatin C, as compared with creatinine, was associated with a reduced risk of all three study outcomes, and reclassification to a lower eGFR was associated with an increased risk. The net reclassification improvement with the measurement of cystatin C, as compared with creatinine, was 0.23 (95% confidence interval [CI], 0.18 to 0.28) for death and 0.10 (95% CI, 0.00 to 0.21) for end-stage renal disease. Results were generally similar for the five cohorts with chronic kidney disease and when both creatinine and cystatin C were used to calculate the eGFR. CONCLUSIONS The use of cystatin C alone or in combination with creatinine strengthens the association between the eGFR and the risks of death and end-stage renal disease across diverse populations.
引用
收藏
页码:932 / 943
页数:12
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