Division of Public Health Sciences, Washington University in St Louis, St Louis, Missouri, USA.
Division of Public Health Sciences, Washington University in St Louis, St Louis, Missouri, USA; Division of Nephrology, Washington University in St Louis, St Louis, Missouri, USA.
Am J Transplant. 2023 May;23(5):629-635. doi: 10.1016/j.ajt.2022.11.005. Epub 2023 Jan 12.
To determine the effect of donor hepatitis C virus (HCV) infection on kidney transplant (KT) outcomes in the era of direct-acting antiviral (DAA) medications, we examined 68,087 HCV-negative KT recipients from a deceased donor between March 2015 and May 2021. A Cox regression analysis was used to estimate adjusted hazard ratios (aHRs) of KT failure, incorporating inverse probability of treatment weighting to control for patient selection to receive an HCV-positive kidney (either nucleic acid amplification test positive [NAT+, n = 2331] or antibody positive (Ab+)/NAT- [n = 1826]) based on recipient characteristics. Compared with kidney from HCV-negative donors, those from Ab+/NAT- (aHR = 0.91; 95% confidence interval [CI], 0.75-1.10) and HCV NAT+ (aHR = 0.89; 95% CI, 0.73-1.08) donors were not associated with an increased risk of KT failure over 3 years after transplant. Moreover, HCV NAT+ kidneys were associated with a higher 1-year estimated glomerular filtration (63.0 vs 61.0 mL/min/1.73 m, P = .007) and lower risk of delayed graft function (aOR = 0.76; 95% CI, 0.68-0.84) compared with HCV-negative kidneys. Our findings suggest that donor HCV positivity is not associated with an elevated risk of graft failure. The inclusion of donor HCV status in the Kidney Donor Risk Index may no longer be appropriate in contemporary practice.
为了确定在直接作用抗病毒(DAA)药物时代供体丙型肝炎病毒(HCV)感染对肾移植(KT)结局的影响,我们检查了 2015 年 3 月至 2021 年 5 月期间来自已故供体的 68087 例 HCV 阴性 KT 受者。使用 Cox 回归分析估计 KT 失败的调整后的危险比(aHR),采用逆概率治疗加权来控制基于受者特征选择接受 HCV 阳性肾脏(核酸扩增试验阳性 [NAT+,n = 2331]或抗体阳性(Ab+)/NAT- [n = 1826])的患者。与 HCV 阴性供体的肾脏相比,Ab+/NAT-(aHR = 0.91;95%置信区间 [CI],0.75-1.10)和 HCV NAT+(aHR = 0.89;95% CI,0.73-1.08)供体的肾脏在移植后 3 年内与 KT 失败的风险增加无关。此外,与 HCV 阴性肾脏相比,HCV NAT+肾脏的 1 年估算肾小球滤过率(63.0 与 61.0 mL/min/1.73 m,P =.007)更高,且延迟移植物功能障碍的风险较低(aOR = 0.76;95% CI,0.68-0.84)。我们的研究结果表明,供体 HCV 阳性与移植物失败的风险增加无关。在当代实践中,供体 HCV 状态纳入肾脏供体风险指数可能不再合适。