A new equation to estimate glomerular filtration rate - PubMed (original) (raw)
A new equation to estimate glomerular filtration rate
Andrew S Levey et al. Ann Intern Med. 2009.
Erratum in
- Ann Intern Med. 2011 Sep 20;155(6):408
Abstract
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.
Conflict of interest statement
Disclosure of conflicts of interest: We have received confirmation from Drs. Levey, Stevens, Schmid, Feldman, Kusek, Eggers, Greene, Coresh and Ms. Zhang that they have returned completed conflicts of interest forms to Annals. We are awaiting confirmation from Dr. Van Lente and Mr. Castro.
Figures
Figure 1. Comparison of performance of Modification of Diet in Renal Disease (MDRD) Study and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations by estimated GFR in the external validation dataset
Panel 1. Measured vs. estimated GFR. Panel 2. Difference between measured and estimated vs. estimated GFR. Shown are smoothed regression line and 95% CI (computed using the lowess smoothing function in R), using quantile regression, excluding lowest and highest 2.5% of estimated GFR values. To convert GFR from mL/min/1.73 m2 to mL/s/m2, multiply by 0.0167.
Comment in
- The CKD-EPI equation and MDRD study equation find similar prevalence of chronic kidney disease in Asian populations.
Sabanayagam C, Wong TY, Tai ES. Sabanayagam C, et al. Ann Intern Med. 2009 Dec 15;151(12):892-3; author reply 893. doi: 10.7326/0003-4819-151-12-200912150-00014. Ann Intern Med. 2009. PMID: 20008766 No abstract available. - [Is there a better equation for estimating glomerular filtration rate based on age and blood creatinine level?].
García López F, Barrio Lucia V. García López F, et al. Nefrologia. 2009;29(6 Suppl):33-5. doi: 10.3265/NEFROLOGIA.2009.29.S.E.noID.36.free. Nefrologia. 2009. PMID: 20221222 Spanish. No abstract available.
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