Houston VA HSR&D Center for Innovations in Quality, Effectiveness and Safety, Michael E DeBakey VA Medical Center, Houston, Texas.
Department of Medicine, Baylor College of Medicine, Houston, Texas.
Aliment Pharmacol Ther. 2019 Jun;49(11):1442-1447. doi: 10.1111/apt.15240. Epub 2019 Apr 1.
Direct-acting anti-viral (DAA) therapy may have a beneficial role in extrahepatic manifestations of hepatitis C virus (HCV) infection. However, the available data are limited.
To examine the effects of DAA treatment on the risk of several extrahepatic manifestations of HCV.
We conducted a retrospective cohort study of patients from the US Department of Veterans Affairs Corporate Data Warehouse who had a positive HCV RNA test and received first course of DAAs between 2012 and 2016. We calculated incidence rates by sustained virological response (SVR) status for six extrahepatic manifestations, and effect of SVR on these conditions was evaluated in adjusted Cox regression models.
Of the 45 260 patients treated with DAA with mean follow-up of 2.01 years, 41 711 (92.2%) experienced SVR. Incidence rates ranged from 0.17/1000 PY for porphyria cutanea tarda to 21.04/1000 PY for diabetes in the SVR group and 0.51/1000 PY for porphyria cutanea tarda to 23.11/1000 PY for diabetes in the no SVR group. The risk was reduced with SVR for mixed cryoglobulinaemia (adjusted HR (aHR) = 0.23; 95% CI 0.10-0.56), glomerulonephritis (aHR = 0.61; 95% CI 0.41-0.90) and lichen planus (aHR = 0.46; 95% CI 0.30-0.70), but not for non-Hodgkin's lymphoma (aHR = 0.86; 95% CI 0.52-1.43) or diabetes (aHR = 0.98; 95% CI 0.81-1.19). Non significant risk reduction was seen for porphyria cutanea tarda (aHR = 0.33; 95% CI 0.11-1.03).
Successful DAA treatment resulting in SVR was associated with significant reductions in the risk of mixed cryoglobulinaemia, glomerulonephritis, lichen planus and possibly porphyria cutanea tarda, but not non-Hodgkin's lymphoma or diabetes.
直接作用抗病毒 (DAA) 治疗可能对丙型肝炎病毒 (HCV) 感染的肝外表现具有有益作用。然而,现有数据有限。
研究 DAA 治疗对 HCV 几种肝外表现的风险的影响。
我们对美国退伍军人事务部公司数据仓库中接受 HCV RNA 检测呈阳性且在 2012 年至 2016 年期间接受首次 DAA 治疗的患者进行了回顾性队列研究。我们按持续病毒学应答 (SVR) 状态计算了六种肝外表现的发病率,并通过调整后的 Cox 回归模型评估了 SVR 对这些疾病的影响。
在接受 DAA 治疗的 45260 名患者中,中位随访时间为 2.01 年,41711 名(92.2%)患者获得 SVR。SVR 组的发病率范围为 0.17/1000 人年的迟发性皮肤卟啉症到 21.04/1000 人年的糖尿病,而无 SVR 组的发病率范围为 0.51/1000 人年的迟发性皮肤卟啉症到 23.11/1000 人年的糖尿病。SVR 与混合性冷球蛋白血症(调整后的 HR[aHR]0.23;95%CI0.10-0.56)、肾小球肾炎(aHR0.61;95%CI0.41-0.90)和扁平苔藓(aHR0.46;95%CI0.30-0.70)的风险降低相关,但与非霍奇金淋巴瘤(aHR0.86;95%CI0.52-1.43)或糖尿病(aHR0.98;95%CI0.81-1.19)无关。迟发性皮肤卟啉症(aHR0.33;95%CI0.11-1.03)的风险降低不具有统计学意义。
导致 SVR 的成功 DAA 治疗与混合性冷球蛋白血症、肾小球肾炎、扁平苔藓和可能的迟发性皮肤卟啉症风险显著降低相关,但与非霍奇金淋巴瘤或糖尿病无关。