A New Equation to Estimate Glomerular Filtration Rate

被引:20241
作者
Levey, Andrew S. [1 ]
Stevens, Lesley A. [1 ]
Schmid, Christopher H. [1 ]
Zhang, Yaping [1 ]
Castro, Alejandro F., III [2 ]
Feldman, Harold I. [3 ]
Kusek, John W. [4 ]
Eggers, Paul [4 ]
Van Lente, Frederick [5 ]
Greene, Tom [6 ]
Coresh, Josef [2 ]
机构
[1] Tufts Med Ctr, Div Nephrol, Boston, MA 02111 USA
[2] Johns Hopkins Univ, Baltimore, MD USA
[3] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[4] NIH, Bethesda, MD 20892 USA
[5] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[6] Univ Utah, Salt Lake City, UT USA
关键词
CHRONIC KIDNEY-DISEASE; COCKCROFT-GAULT EQUATIONS; RENIN-ANGIOTENSIN SYSTEM; SERUM CREATININE; RENAL-DISEASE; PREDICTIVE PERFORMANCE; DIABETIC-PATIENTS; NATIONAL-HEALTH; DUAL BLOCKADE; CYSTATIN-C;
D O I
10.7326/0003-4819-150-9-200905050-00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Equations to estimate glomerular filtration rate (GFR) are routinely used to assess kidney function. Current equations have limited precision and systematically underestimate measured GFR at higher values. Objective: To develop a new estimating equation for GFR: the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Design: Cross-sectional analysis with separate pooled data sets for equation development and validation and a representative sample of the U. S. population for prevalence estimates. Setting: Research studies and clinical populations ("studies") with measured GFR and NHANES (National Health and Nutrition Examination Survey), 1999 to 2006. Participants: 8254 participants in 10 studies (equation development data set) and 3896 participants in 16 studies (validation data set). Prevalence estimates were based on 16 032 participants in NHANES. Measurements: GFR, measured as the clearance of exogenous filtration markers (iothalamate in the development data set; iothalamate and other markers in the validation data set), and linear regression to estimate the logarithm of measured GFR from standardized creatinine levels, sex, race, and age. Results: In the validation data set, the CKD-EPI equation performed better than the Modification of Diet in Renal Disease Study equation, especially at higher GFR (P < 0.001 for all subsequent comparisons), with less bias (median difference between measured and estimated GFR, 2.5 vs. 5.5 mL/min per 1.73 m(2)), improved precision (interquartile range [IQR] of the differences, 16.6 vs. 18.3 mL/min per 1.73 m(2)), and greater accuracy (percentage of estimated GFR within 30% of measured GFR, 84.1% vs. 80.6%). In NHANES, the median estimated GFR was 94.5 mL/min per 1.73 m(2) ( IQR, 79.7 to 108.1) vs. 85.0 (IQR, 72.9 to 98.5) mL/min per 1.73 m(2), and the prevalence of chronic kidney disease was 11.5% (95% CI, 10.6% to 12.4%) versus 13.1% (CI, 12.1% to 14.0%). Limitation: The sample contained a limited number of elderly people and racial and ethnic minorities with measured GFR. Conclusion: The CKD-EPI creatinine equation is more accurate than the Modification of Diet in Renal Disease Study equation and could replace it for routine clinical use. Primary Funding Source: National Institute of Diabetes and Digestive and Kidney Diseases.
引用
收藏
页码:604 / 612
页数:9
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