A New Equation to Estimate Glomerular Filtration Rate
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Supplemental Material
Appendix Figure 1. Flow chart showing development of the CKD-EPI pooled creatinine database.
Appendix Table 1. Category 1: Studies and Participant Characteristics
Appendix Table 2. Category 2: Studies and Participant Characteristics
Appendix Table 3. Model Families
Appendix Table 4. Definition of Model Types
Appendix Table 5. Forms of Variables and Coefficients in the CKD-EPI and MDRD Study Equations
Appendix Table 6. Comparison of Performance of MDRD Study and CKD-EPI Equations
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A New Equation to Estimate Glomerular Filtration Rate. Ann Intern Med.2009;150:604-612. [Epub 5 May 2009]. doi:10.7326/0003-4819-150-9-200905050-00006
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Prevalence of chronic kidney disease by the new CKD-EPI and the MDRD study equations in Asians
To the Editor: Levey and colleagues presented a new equation for estimation of GFR, the CKD-EPI (1) and compared the prevalence of CKD in the US population estimated by the new equation with that by the MDRD study equation. The authors reported that the new CKD-EPI equation gives a lower estimated prevalence of CKD than the MDRD study equation and suggested that this new equation should also be tested in other ethnic groups. Recent studies in Asian populations show that the epidemiological pattern and the relative contribution of some of the known risk factors of CKD such as blood pressure (2) and body mass index (3) are different among Asians compared to Western populations. We examined the prevalence of CKD by MDRD study equation (4) and the new CKD-EPI equation, (1) in a multi-ethnic Asian population (n=4,498) comprising of Chinese (66.7%), Malay (17.5%) and Indian (15.8%) participants aged ¡Ã24years, who participated in the Singapore Prospective Study Programme (SP2), a population-based cross-sectional study in Singapore (5). We defined CKD as estimated GFR <60 mL/min/1.73 m2 or micro/macroalbuminuria (urinary albumin-to-creatinine ratio ¡Ã17mg/g for men and ¡Ã25mg/g for women). In keeping with the results from Levey et al., the median estimated GFR by CKD-EPI was 3.7 mL/min/1.73m2 higher than that by MDRD but the prevalence of CKD was similar using both equations (21.5% vs. 21.7% comparing CKD-EPI and MDRD). The prevalence of CKD estimated by both equations was similar in Chinese (18.5 vs. 18.6, comparing CKD-EPI and MDRD), Malay (28.5 vs.28.6) and Indian (26.7 vs. 27.0) participants. However, as compared to MDRD, the CKD -EPI equation leads to a higher prevalence of stage 1 (7.1 vs. 6.5), a lower prevalence of stage 2 (8.3 vs. 9.1) and a similar prevalence of stage 3 and above (6.1% vs. 6.2%) CKD categories; this pattern was seen in all three Asian ethnic groups. Although we did not have a gold standard measurement for GFR to compare the performance of the two equations, our study indicates that the new CKD-EPI equation is broadly useful for estimating CKD prevalence in three common racial ethnic groups in Asia.
References
1. Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, III, Feldman HI et al. A new equation to estimate glomerular filtration rate. Ann Intern Med 2009; 150: 604-12.
2. Ramirez SP, McClellan W, Port FK, Hsu SIH. Risk Factors for Proteinuria in a Large, Multiracial, Southeast Asian Population. J Am Soc Nephrol 2002; 13: 1907-17.
3. Shankar A, Leng C, Chia KS, Koh D, Tai ES, Saw SM et al. Association between body mass index and chronic kidney disease in men and women: population-based study of Malay adults in Singapore. Nephrol Dial Transplant 2008; 23: 1910-8.
4. Froissart M, Rossert J, Jacquot C, Paillard M, Houillier P. Predictive performance of the modification of diet in renal disease and Cockcroft-Gault equations for estimating renal function. J Am Soc Nephrol 2005; 16: 763-73.
5. Nang EE, Khoo CM, Tai ES, Lim SC, Tavintharan S, Wong TY et al. Is There a Clear Threshold for Fasting Plasma Glucose That Differentiates Between Those With and Without Neuropathy and Chronic Kidney Disease?: The Singapore Prospective Study Program. Am J Epidemiol 2009.
Conflict of Interest:
None declared
GFR estimation using the CKD-EPI equation
Dr. Wong reports that mean estimated GFR computed using the CKD-EPI equation is higher than using the MDRD Study equation in a young Asian population (presumably with high GFR) of mixed ethnicity. This result confirms our findings in a predominantly US and European population (1) and is expected due to the form and coefficients for the variables for both equations. Studies with measured GFR are required to evaluate the accuracy of GFR estimates in Asian populations. There is no "Asian coefficient" for the CKD-EPI equation, so we suspect it will not be as accurate in Asians as in our study. Others have proposed coefficients for use of the MDRD Study in China and Japan, but the results are not consistent (2, 3), and we suggest further studies in these populations. Unlike our report, Dr. Wong does not find a large difference in the prevalence of chronic kidney disease (CKD) using the CKD-EPI equation compared to the MDRD Study equation. CKD prevalence estimates depend on many factors other than the estimating equation, including the assay for serum creatinine, the distribution of measured GFR in the study population, the distribution of age, sex and race (factors that are included in the equations), and non-GFR determinants of serum creatinine, such as muscle mass and diet (factors that are not included in the equations) (4). CKD prevalence is also affected by markers to assess kidney damage. Using the CKD-EPI equation, the prevalence of CKD Stages 3 -4 in Dr. Wong's study was only slightly lower than in the US (6.1% vs. 6.7% in our report) despite a lower mean age, but the prevalence of CKD Stages 1 and 2 was substantially higher (15.4% vs. 5.8% in our report) (Appendix Table 9). The latter finding is at least partially due to one- time ascertainment for urine albumin-to-creatinine ratio rather than our method of accounting for persistence in only a subset of individuals with microalbuminuria (5). As we noted, because of the higher mean estimated GFR, the prevalence ratio of CKD Stages 1 to 2 in Dr. Wong's study was higher using the CKD-EPI equation than using the MDRD Study equation. We encourage others to compare the performance of the CKD-EPI equation to the MDRD Study equation in estimating measured GFR, in assessing CKD prevalence, and in predicting risk of future events as part of the process of improving GFR estimation and understanding its clinical implications.
References:
1. Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF, 3rd, Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):604-12.
2. Matsuo S, Imai E, Horio M, Yasuda Y, Tomita K, Nitta K, et al. Revised Equations for Estimated GFR From Serum Creatinine in Japan. Am J Kidney Dis. 2009; 53: 982-992.
3. Rule AD, Wee TB. Glomerular Filtration Rate estimation in Japan and China: what accounts for the difference? Am J Kidney Dis. 2009; 53: 932-5.
4. Stevens LA, Coresh J, Greene T, Levey AS. Assessing kidney function-- measured and estimated glomerular filtration rate. N Engl J Med. 2006;354(23):2473-83.
5. Coresh J, Selvin E, Stevens LA, Manzi J, Kusek J, Eggers PW, et al. Prevalence of chronic kidney disease in the United States. JAMA. 2007;298(17):2038-47.
Conflict of Interest:
None declared