Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
Department of Gastroenterology, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2022 May 13;17(5):e0268478. doi: 10.1371/journal.pone.0268478. eCollection 2022.
Direct-acting antivirals (DAA) are highly effective at treating Hepatitis C virus (HCV) infection, with a cure rate >95%. However, the effect of DAAs on kidney function remains debated.
We analyzed electronic health record data for DAA-naive patients with chronic HCV infection engaged in HCV care at Boston Medical Center between 2014 and 2018. We compared the following hypothetical interventions using causal inference methods: 1) initiation of DAA and 2) no DAA initiation. For patients with normal kidney function at baseline (eGFR>90 ml/min/1.73m2), we estimated and compared the risk for reaching Stage 3 chronic kidney disease (CKD) (eGFR≤60 ml/min/1.73m2) under each intervention. For patients with baseline CKD Stages 2-4 (15<eGFR≤90 ml/min/1.73m2), we estimated and compared the mean change in eGFR at 2 years after baseline under each intervention. We used the parametric g-formula to adjust our estimates for baseline and time-varying confounders.
First, among 1390 patients with normal kidney function at baseline the estimated 2-year risk difference (95% CI) of reaching Stage 3 CKD for DAA initiation versus no DAA was -1% (-3, 2). Second, among 733 patients with CKD Stage 2-4 at baseline the estimated 2-year mean difference in change in eGFR for DAA initiation versus no DAA therapy was -3 ml/min/1.73m2 (-8, 2).
We found no effect of DAA initiation on kidney function, independent of baseline renal status. This suggests that DAAs may not be nephrotoxic; furthermore, in the short-term, HCV clearance may not improve CKD.
直接作用抗病毒药物(DAA)在治疗丙型肝炎病毒(HCV)感染方面非常有效,治愈率>95%。然而,DAA 对肾功能的影响仍存在争议。
我们分析了 2014 年至 2018 年间在波士顿医疗中心接受 HCV 治疗的 DAA 初治慢性 HCV 感染患者的电子健康记录数据。我们使用因果推理方法比较了以下两种假设干预措施:1)开始使用 DAA 和 2)不开始使用 DAA。对于基线时肾功能正常的患者(eGFR>90ml/min/1.73m2),我们分别估计并比较了两种干预措施下达到慢性肾脏病(CKD)第 3 期(eGFR≤60ml/min/1.73m2)的风险。对于基线 CKD 第 2-4 期的患者(15<eGFR≤90ml/min/1.73m2),我们分别估计并比较了两种干预措施下基线后 2 年 eGFR 的平均变化。我们使用参数 g 公式调整了我们对基线和随时间变化的混杂因素的估计。
首先,在 1390 名基线肾功能正常的患者中,与不使用 DAA 相比,开始使用 DAA 的 2 年风险差异(95%CI)为-1%(-3,2)。其次,在 733 名基线 CKD 第 2-4 期的患者中,与不使用 DAA 相比,开始使用 DAA 的 2 年 eGFR 变化的平均差异为-3ml/min/1.73m2(-8,2)。
我们发现无论基线肾脏状况如何,开始使用 DAA 对肾功能均无影响。这表明 DAA 可能没有肾毒性;此外,在短期内,HCV 清除可能不会改善 CKD。