Kidney Health Research Collaborative, Department of Medicine, University of California, San Francisco, California, USA.
Division of Nephrology, Department of Medicine, University of California, San Francisco, California, USA.
Clin Infect Dis. 2023 Feb 8;76(3):461-468. doi: 10.1093/cid/ciac731.
The impact of adopting a race-free estimated glomerular filtration rate (eGFR) creatinine (eGFRcr) equation on racial differences in chronic kidney disease (CKD) progression among people with human immunodeficiency virus (PWH) is unknown.
We defined eGFR stages using the original race-adjusted Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) eGFRcr equation and the new race-free CKD-EPI eGFRcr equation. We then estimated 5-year probabilities of transitioning from baseline kidney function to more advanced eGFR stages and examined the association of race (black vs white) with rates of CKD progression using Markov models.
With the race-adjusted eGFRcr equation, black participants (n = 31 298) had a lower risk of progressing from eGFR stage 1 to 2 (hazard ratio [HR], 0.77; 95% confidence interval [CI], .73-.82), an equal risk of progressing from stage 2 to 3 (1.00; .92-.07) and a 3-fold risk of progressing from stage 3 to 4 or 5 (3.06; 2.60-3.62), compared with white participants (n = 27 542). When we used the race-free eGFRcr equation, 16% of black participants were reclassified into a more severe eGFR stage at baseline. The reclassified black individuals had a higher prevalence of CKD risk factors than black PWH who were not reclassified. With the race-free eGFRcr equation, black participants had a higher risk of disease progression across all eGFR stages than white participants.
The original eGFRcr equation systematically masked a subgroup of black PWH who are at high-risk of CKD progression. The new race-free eGFRcr equation unmasks these individuals and may allow for earlier detection and management of CKD.
采用无种族估算肾小球滤过率(eGFR)肌酐(eGFRcr)方程对艾滋病毒(HIV)感染者(PWH)慢性肾脏病(CKD)进展中种族差异的影响尚不清楚。
我们使用原始种族调整的慢性肾脏病流行病学合作(CKD-EPI)eGFRcr 方程和新的无种族的 CKD-EPI eGFRcr 方程来定义 eGFR 分期。然后,我们估计了从基线肾功能到更严重的 eGFR 分期的 5 年转移概率,并使用马尔可夫模型检查了种族(黑人与白人)与 CKD 进展速度的关系。
使用种族调整的 eGFRcr 方程,黑人参与者(n = 31298)从 eGFR 阶段 1 进展到 2 的风险较低(风险比 [HR],0.77;95%置信区间 [CI],0.73-0.82),从阶段 2 进展到 3 的风险相等(1.00;0.92-0.07),从阶段 3 进展到 4 或 5 的风险增加 3 倍(3.06;2.60-3.62),与白人参与者(n = 27542)相比。当我们使用无种族的 eGFRcr 方程时,16%的黑人参与者在基线时被重新分类为更严重的 eGFR 阶段。重新分类的黑人个体比未重新分类的黑人 HIV 感染者具有更高的 CKD 危险因素患病率。使用无种族的 eGFRcr 方程,黑人参与者在所有 eGFR 阶段的疾病进展风险均高于白人参与者。
原始的 eGFRcr 方程系统地掩盖了一组黑人 HIV 感染者中 CKD 进展风险较高的亚组。新的无种族的 eGFRcr 方程揭示了这些个体,可能有助于更早地发现和管理 CKD。