King Edward Hospital Renal Clinic, Department of Nephrology, Division of Medicine, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Int Urol Nephrol. 2012 Jun;44(3):847-55. doi: 10.1007/s11255-011-9928-7. Epub 2011 Mar 5.
South African guidelines for early detection and management of chronic kidney disease (CKD) recommend using the Cockcroft-Gault (CG) or Modification of Diet in Renal Disease (MDRD) equations for calculating estimated glomerular filtration rate (eGFR) with the correction factor, 1.212, included for MDRD-eGFR in black patients. We compared eGFR against technetium-99m-diethylenetriaminepentaacetic acid ((99m)Tc-DTPA) imaging.
Using clinical records, we retrospectively recorded demographic, clinical, and laboratory data as well as (99m)Tc-DTPA-measured GFR (mGFR) results obtained from routine visits. Data from 148 patients of African (n = 91) and Indian (n = 57) ancestry were analyzed.
Median (IQR) mGFR was 38.5 (44) ml/min/1.73 m(2), with no statistical difference between African and Indian patients (P = 0. 573). In African patients with stage 3 CKD, MDRD-eGFR (unadjusted for black ethnicity) overestimated mGFR by 5.3% [2.0 (16.0) ml/min/1.73 m(2)] compared to CG-eGFR and MDRD-eGFR (corrected for black ethnicity) that overestimated mGFR by 17.7% [6.0 (15.0) ml/min/1.73 m(2)] and 17.1% [6.0 (17.5) ml/min/1.73 m(2)], respectively. In stage 1-2, CKD eGFR overestimated mGFR by 52.5, 38.0, and 19.3% for CG, MDRD (ethnicity-corrected), and MDRD (without correction), respectively. In Indian stage 3 CKD patients, MDRD-eGFR underestimated mGFR by 35.6% [-21.0 (6.5) ml/min/1.73 m(2)] and CG-eGFR by 4.4% [-2.0 (27.0) ml/min/1.73 m(2)], while in stage 1-2 CKD, CG-eGFR and MDRD-eGFR overestimated mGFR by 13.8 and 6.3%, respectively.
MDRD-eGFR calculated without the African-American correction factor improved GFR prediction in African CKD patients and using the MDRD correction factor of 1.0 in Indian patients as in Caucasians may be inappropriate.
南非慢性肾脏病(CKD)早期检测和管理指南建议使用 Cockcroft-Gault(CG)或肾脏病饮食改良公式(MDRD)来计算肾小球滤过率(eGFR),并对黑人患者的 MDRD-eGFR 采用 1.212 的校正系数。我们将 eGFR 与锝-99m-二乙三胺五乙酸((99m)Tc-DTPA)显像进行了比较。
我们使用临床记录回顾性地记录了人口统计学、临床和实验室数据以及从常规就诊中获得的(99m)Tc-DTPA 测量的肾小球滤过率(mGFR)结果。对来自 148 名非洲裔(n=91)和印度裔(n=57)患者的数据进行了分析。
中位(IQR)mGFR 为 38.5(44)ml/min/1.73 m2,非洲裔和印度裔患者之间无统计学差异(P=0.573)。在南非 3 期 CKD 患者中,未校正非裔人群的 MDRD-eGFR 比 CG-eGFR 高估 mGFR 5.3%[2.0(16.0)ml/min/1.73 m2],而校正非裔人群的 MDRD-eGFR 高估 mGFR 17.7%[6.0(15.0)ml/min/1.73 m2]和 17.1%[6.0(17.5)ml/min/1.73 m2]。在 1-2 期 CKD 中,CG、MDRD(校正种族)和 MDRD(未校正)eGFR 分别高估了 mGFR 52.5%、38.0%和 19.3%。在印度 3 期 CKD 患者中,MDRD-eGFR 低估了 mGFR 35.6%[-21.0(6.5)ml/min/1.73 m2],CG-eGFR 低估了 mGFR 4.4%[-2.0(27.0)ml/min/1.73 m2],而在 1-2 期 CKD 中,CG-eGFR 和 MDRD-eGFR 分别高估了 mGFR 13.8%和 6.3%。
在南非 CKD 患者中,不使用非裔美国人校正因子计算的 MDRD-eGFR 改善了 GFR 预测,而在印度患者中使用 MDRD 校正因子 1.0 可能不适合,就像在白种人一样。