The effects of sustained virological response to direct‐acting anti‐viral therapy on the risk of extrahepatic manifestations of hepatitis C infection

医学 迟发性皮肤卟啉症 内科学 胃肠病学 入射(几何) 丙型肝炎 糖尿病 丙型肝炎病毒 回顾性队列研究 比例危险模型 队列 免疫学 病毒 内分泌学 物理 光学
作者
Hashem B. El‐Serag,Israel C. Christie,Amy Puenpatom,Diana Castillo,Fasiha Kanwal,Jennifer R. Kramer
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:49 (11): 1442-1447 被引量:59
标识
DOI:10.1111/apt.15240
摘要

Summary Background 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. Aim To examine the effects of DAA treatment on the risk of several extrahepatic manifestations of HCV. Methods 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. Results 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). Conclusions 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.

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