Abstract

BackgroundHepatitis C virus (HCV)-infected patients with chronic kidney disease (CKD) have rarely been studied because they rarely accept interferon-based therapy (IBT) and have been difficult to follow up. We investigated long-term outcomes of IBT on the population.MethodsThis population-based cohort study used the Taiwan National Health Insurance Research Database as its data source. HCV patients diagnosed with CKD between Jan. 1, 2003, and Dec. 31, 2013, were selected. They were then divided into two groups based on whether they had undergone IBT. All-cause mortality, acute myocardial infarction (AMI), ischemic stroke (IS), hemorrhagic stroke, and new-onset dialysis were evaluated using a Cox proportional hazard regression analysis after propensity score matching.ResultsWe enrolled 9872 HCV patients with CKD: 1684 patients in the treated cohort and 8188 patients in the untreated cohort. The annual incidence of all-cause mortality (19.00 vs. 42.89 events per 1000 person-years; p < 0.001) and the incidences of hemorrhagic stroke (1.21 vs. 4.19 events per 1000 person-years; p = 0.006) were lower in the treated cohort. New-onset dialysis was also lower in the treated cohort (aHR: 0.31; 95% CI: 0.20–0.48; p < 0.001).ConclusionAntiviral therapy might provide protective benefits on all-cause mortality, hemorrhagic stroke, and new-onset dialysis in HCV-infected patients with CKD.

Highlights

  • Hepatitis C virus (HCV)-infected patients with chronic kidney disease (CKD) have rarely been studied because they rarely accept interferon-based therapy (IBT) and have been difficult to follow up

  • Baseline characteristics of the study population We identified 17,792 HCV-infected patients with CKD among the 242,568 patients diagnosed with HCV

  • The pre-propensity score matching (PSM) treated HCV patients had a higher prevalence of diabetes and hypertension and they tended to receive oral hypoglycemia agents and Angiotensin converting enzyme inhibitor (ACEi)/Angiotensin receptor blocker (ARB) other than CCB

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Summary

Introduction

Hepatitis C virus (HCV)-infected patients with chronic kidney disease (CKD) have rarely been studied because they rarely accept interferon-based therapy (IBT) and have been difficult to follow up. Hepatitis C virus (HCV), which has a 2.8 ~ 3.0% prevalence worldwide, is strongly associated with major liver decompensation [1]. Chronic hepatitis C viral infection (CHC) is strongly associated with end-stage renal disease (ESRD) [2] via extrahepatic metabovascular and immunological complications such as vasculitis, cryoglobulinemia, and glomerulonephritis [3]. Pegylated interferon-based therapy (IBT), a combination of pegylated interferon plus ribavirin, protected HCV patients against liver cirrhosis and hepatocellular carcinoma (HCC) [7], and successful viral eradication reduced cardiovascular events and late dialysis in HCV patients without CKD [8, 9].

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