Key result
The estimated prevalence of chronic kidney disease in an urban black South African population varied from 2.0% using the Cockcroft-Gault formula to 5.9% using the CKD-EPI creatinine-cystatin C equation.
Why the study?
The prevalence, distribution, concordance, and associations of chronic kidney disease determined by five GFR formulae in urban black residents of Cape Town were not established.
Cross-Sectional (n=1,092)
The prevalence of CKD varies significantly depending on the GFR equation used, highlighting the need for accurate diagnostic tools and routine screening in high-risk patients.
CKD prevalence estimates vary by GFR equation; leaves open optimal formula for population screening and research standardization.
Background To determine the prevalence, distribution, concordance and associations of chronic kidney disease (CKD) determined by five glomerular filtration rate (GFR) formulae in urban black residents of Cape Town. Methods Data collection in this cross-sectional study included interviews, clinical measurements and biochemical analyses, including serum creatinine and cystatin C levels. GFR was based on the CKD Epidemiology Collaboration (CKD-EPI) equations (CKD-EPI creatinine (CKD-EPIcr), CKD-EPI cystatin C (CKD-EPIcys), CKD-EPI creatinine-cystatins (CKD-EPIcr-cys)), Modification of Diet in Renal Disease (MDRD) and Cockcroft-Gault formula (CGF). GFR < 60 mL/min/1.73 m2 defined CKD. Results Among 392 men and 700 women, mean GFR, was between 114.0 (CKD-EPIcr) and 135.4 mL/min/1.73 m2 (CGF) in men, and between 107.5 (CKD-EPIcr-cys) and 173.4 mL/min/1.73 m2 (CGF) in women. CKD prevalence ranged from 2.3% (CKD-EPIcr and MDRD) to 5.1% (CKD-EPIcys) in men and 1.6% (CGF) to 6.7% (CKD-EPIcr-cys) in women. The kappa statistic was high between CKD-EPIcr and MDRD (0.934), and CKD-EPIcys and CKD-EPIcr-cys (0.815), but fair-to-moderate between the other eqs. (0.353–0.565). In the basic regressions, older age and body mass index ≥30 kg/m2, but not gender, were significantly associated with CKD-EPIcr-defined CKD. In the presence of these three variables, hypertension, heart rate ≥ 90 beats/minute, diabetes and low-density lipoprotein cholesterol were significant predictors of prevalent CKD. Conclusions Varying CKD prevalence estimates, because of different GFR equations used, underscores the need to improve accuracy of CKD diagnoses. Furthermore, screening for CKD should be incorporated into the routine assessment of high-risk patients such as those with hypertension or diabetes.
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Peer et al. (2020) conducted a cross-sectional in Chronic kidney disease (n=1,092). Five GFR estimating equations (CKD-EPIcr, CKD-EPIcys, CKD-EPIcr-cys, MDRD, Cockcroft-Gault) was evaluated on Prevalence of chronic kidney disease (eGFR < 60 mL/min/1.73 m2). The estimated prevalence of chronic kidney disease in an urban black South African population varied from 2.0% using the Cockcroft-Gault formula to 5.9% using the CKD-EPI creatinine-cystatin C equation.
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