TY - JOUR
T1 - Racial disparities in creatinine-based kidney function estimates among HIV-infected adults
AU - Anker, Naomi
AU - Scherzer, Rebecca
AU - Peralta, Carmen
AU - Powe, Neil
AU - Banjeree, Tanushree
AU - Shlipak, Michael
N1 - Publisher Copyright:
© 2016 by ISHIB.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Objective: The aim of our study was to investigate whether current eGFR equations in clinical use might systematically overestimate the kidney function, and thus misclassify CKD status, of Black Americans with HIV. Specifically, we evaluated the impact of removing the race coefficient from the MDRD and CKD-EPI equations on comparisons between Black and White HIV-infected veterans related to: 1) the prevalence of reduced eGFR; 2) the distribution of eGFR values; and 3) the relationship between eGFR and all-cause mortality. Design: Retrospective cohort study. Setting: The Department of Veterans Affairs (VA) HIV Clinical Case Registry (CCR), which actively monitors all HIV-infected persons receiving care in the VA nationally. Patients/Participants: 21,905 treatmentnaïve HIV-infected veterans. Main Outcome Measures: Estimated glomerular filtration rate (eGFR) using the abbreviated Modification of Diet in Renal Disease (MDRD) formula with and without (MDRD-RCR) the race coefficient and allcause mortality. Results: Persons with eGFR <45 mL/ min/1.73m2 had a higher risk of death compared with those with eGFR >80 mL/ min/1.73m2 among both Blacks (HR=2.8, 95%CI: 2.4-3.3) and Whites (HR=1.9, 95%CI: 1.4-2.6), but the association appeared to be stronger in Blacks (P=.038, test for interaction). Blacks with eGFR 45- 60 mL/min/1.73m2 also had a higher risk of death (HR=1.7, 95%CI: 1.4-2.1) but Whites did not (HR=0.86, 95%CI: .67- 1.10; test for interaction: P<.0001). Racial differences were substantially attenuated when eGFR was re-calculated without the race coefficient. Conclusions: Our findings suggest that clinicians may want to consider estimating glomerular filtration rate without the race coefficient in Blacks with HIV.
AB - Objective: The aim of our study was to investigate whether current eGFR equations in clinical use might systematically overestimate the kidney function, and thus misclassify CKD status, of Black Americans with HIV. Specifically, we evaluated the impact of removing the race coefficient from the MDRD and CKD-EPI equations on comparisons between Black and White HIV-infected veterans related to: 1) the prevalence of reduced eGFR; 2) the distribution of eGFR values; and 3) the relationship between eGFR and all-cause mortality. Design: Retrospective cohort study. Setting: The Department of Veterans Affairs (VA) HIV Clinical Case Registry (CCR), which actively monitors all HIV-infected persons receiving care in the VA nationally. Patients/Participants: 21,905 treatmentnaïve HIV-infected veterans. Main Outcome Measures: Estimated glomerular filtration rate (eGFR) using the abbreviated Modification of Diet in Renal Disease (MDRD) formula with and without (MDRD-RCR) the race coefficient and allcause mortality. Results: Persons with eGFR <45 mL/ min/1.73m2 had a higher risk of death compared with those with eGFR >80 mL/ min/1.73m2 among both Blacks (HR=2.8, 95%CI: 2.4-3.3) and Whites (HR=1.9, 95%CI: 1.4-2.6), but the association appeared to be stronger in Blacks (P=.038, test for interaction). Blacks with eGFR 45- 60 mL/min/1.73m2 also had a higher risk of death (HR=1.7, 95%CI: 1.4-2.1) but Whites did not (HR=0.86, 95%CI: .67- 1.10; test for interaction: P<.0001). Racial differences were substantially attenuated when eGFR was re-calculated without the race coefficient. Conclusions: Our findings suggest that clinicians may want to consider estimating glomerular filtration rate without the race coefficient in Blacks with HIV.
KW - Chronic Kidney Disease
KW - Estimated Glomerular Filtration Rate
KW - Human Immunodeficiency Virus
KW - Mortality
KW - Racial Disparities
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U2 - 10.18865/ed.26.2.213
DO - 10.18865/ed.26.2.213
M3 - Article
C2 - 27103772
AN - SCOPUS:84964988344
SN - 1049-510X
VL - 26
SP - 213
EP - 220
JO - Ethnicity and Disease
JF - Ethnicity and Disease
IS - 2
ER -