British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada; School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
J Hepatol. 2019 Dec;71(6):1116-1125. doi: 10.1016/j.jhep.2019.07.021. Epub 2019 Aug 6.
BACKGROUND & AIMS: HCV infection is associated with several extrahepatic manifestations (EHMs). We evaluated the impact of sustained virological response (SVR) on the risk of 7 EHMs that contribute to the burden of extrahepatic disease: type 2 diabetes mellitus, chronic kidney disease or end-stage renal disease, stroke, ischemic heart disease, major adverse cardiac events, mood and anxiety disorders, and rheumatoid arthritis.
A longitudinal cohort study was conducted using data from the British Columbia Hepatitis Testers Cohort, which included ~1.3 million individuals screened for HCV. We identified all HCV-infected individuals who were treated with interferon-based therapies between 1999 and 2014. SVR was defined as a negative HCV RNA test ≥24 weeks post-treatment or after end-of-treatment, if unavailable. We computed adjusted subdistribution hazard ratios (asHR) for the effect of SVR on each EHM using competing risk proportional hazard models. Subgroup analyses by birth cohort, sex, injection drug exposure and genotype were also performed.
Overall, 10,264 HCV-infected individuals were treated with interferon, of whom 6,023 (59%) achieved SVR. Compared to those that failed treatment, EHM risk was significantly reduced among patients with SVR for type 2 diabetes mellitus (asHR 0.65; 95%CI 0.55-0.77), chronic kidney disease or end-stage renal disease (asHR 0.53; 95% CI 0.43-0.65), ischemic or hemorrhagic stroke (asHR 0.73; 95%CI 0.49-1.09), and mood and anxiety disorders (asHR 0.82; 95%CI 0.71-0.95), but not for ischemic heart disease (asHR 1.23; 95%CI 1.03-1.47), major adverse cardiac events (asHR 0.93; 95%CI 0.79-1.11) or rheumatoid arthritis (asHR 1.09; 95% CI 0.73-1.64).
SVR was associated with a reduction in the risk of several EHMs. Increased uptake of antiviral therapy may reduce the growing burden of EHMs in this population.
We estimated the rates of chronic comorbidities other than liver disease between those who were cured and those who failed treatment for hepatitis C virus (HCV) infection. Our findings showed that the rates of these non-liver diseases were largely reduced for those who were cured with interferon-based treatments. Early HCV treatments could provide many benefits in the prevention of various HCV complications beyond liver disease.
HCV 感染与多种肝外表现(EHMs)相关。我们评估了持续病毒学应答(SVR)对 7 种导致肝外疾病负担的 EHMs 的风险的影响:2 型糖尿病、慢性肾脏病或终末期肾病、中风、缺血性心脏病、主要不良心脏事件、情绪和焦虑障碍以及类风湿关节炎。
使用不列颠哥伦比亚省肝炎检测者队列的数据进行了一项纵向队列研究,该队列包括约 130 万例筛查 HCV 的个体。我们确定了所有在 1999 年至 2014 年期间接受基于干扰素治疗的 HCV 感染个体。SVR 定义为治疗后 24 周或治疗结束后 HCV RNA 检测阴性≥24 周,如不可用。我们使用竞争风险比例风险模型计算了 SVR 对每种 EHM 的影响的调整亚分布危险比(asHR)。还进行了按出生队列、性别、注射药物暴露和基因型进行的亚组分析。
总体而言,有 10264 例 HCV 感染个体接受了干扰素治疗,其中 6023 例(59%)达到 SVR。与治疗失败的个体相比,SVR 患者的 2 型糖尿病(asHR 0.65;95%CI 0.55-0.77)、慢性肾脏病或终末期肾病(asHR 0.53;95%CI 0.43-0.65)、缺血性或出血性中风(asHR 0.73;95%CI 0.49-1.09)和情绪和焦虑障碍(asHR 0.82;95%CI 0.71-0.95)的 EHM 风险显著降低,但缺血性心脏病(asHR 1.23;95%CI 1.03-1.47)、主要不良心脏事件(asHR 0.93;95%CI 0.79-1.11)或类风湿关节炎(asHR 1.09;95%CI 0.73-1.64)的风险无显著降低。
SVR 与降低几种 EHM 的风险相关。增加抗病毒治疗的使用率可能会降低该人群中 EHM 的不断增长的负担。
我们估计了治愈组和治疗失败组 HCV 感染者除肝脏疾病以外的慢性合并症的发生率。我们的研究结果表明,对于那些接受基于干扰素的治疗而治愈的患者,这些非肝脏疾病的发生率大幅降低。早期 HCV 治疗可能会在预防除肝脏疾病以外的各种 HCV 并发症方面带来许多益处。