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Eradication of hepatitis C virus and non‐liver‐related non–acquired immune deficiency syndrome–related events in human immunodeficiency virus/hepatitis C virus coinfection

机译:消除人类免疫缺陷病毒/丙型肝炎病毒合并感染中的丙型肝炎病毒和非肝相关性非获得性免疫缺陷综合症相关事件

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摘要

We assessed non‐liver‐related non–acquired immunodeficiency syndrome (AIDS)‐related (NLR‐NAR) events and mortality in a cohort of human immunodeficiency virus (HIV)/hepatitis C virus (HCV)–coinfected patients treated with interferon (IFN) and ribavirin (RBV), between 2000 and 2008. The censoring date was May 31, 2014. Cox regression analysis was performed to assess the adjusted hazard rate (HR) of overall death in responders and nonresponders. Fine and Gray regression analysis was conducted to determine the adjusted subhazard rate (sHR) of NLR deaths and NLR‐NAR events considering death as the competing risk. The NLR‐NAR events analyzed included diabetes mellitus, chronic renal failure, cardiovascular events, NLR‐NAR cancer, bone events, and non‐AIDS‐related infections. The variables for adjustment were age, sex, past AIDS, HIV transmission category, nadir CD4+ T‐cell count, antiretroviral therapy, HIV RNA, liver fibrosis, HCV genotype, and exposure to specific anti‐HIV drugs. Of the 1,625 patients included, 592 (36%) had a sustained viral response (SVR). After a median 5‐year follow‐up, SVR was found to be associated with a significant decrease in the hazard of diabetes mellitus (sHR, 0.57; 95% confidence interval [CI], 0.35‐0.93; P = 0.024) and decline in the hazard of chronic renal failure close to the threshold of significance (sHR, 0.43; 95% CI, 0.17‐1.09; P = 0.075). Conclusion: Our data suggest that eradication of HCV in coinfected patients is associated not only with a reduction in the frequency of death, HIV progression, and liver‐related events, but also with a reduced hazard of diabetes mellitus and possibly of chronic renal failure. These findings argue for the prescription of HCV therapy in coinfected patients regardless of fibrosis stage. (Hepatology 2017;66:344–356).
机译:我们评估了一组人类免疫缺陷病毒(HIV)/丙型肝炎病毒(HCV)合并感染的干扰素(IFN)治疗患者的非肝相关性非获得性免疫缺陷综合症(AIDS)相关性(NLR-NAR)事件和死亡率)和利巴韦林(RBV)之间的比较,检查日期为2014年5月31日。检查时间为2014年5月31日。进行了Cox回归分析,以评估调整后的反应者和未反应者的总体死亡危险率(HR)。进行了精细和灰色回归分析,以确定将死亡作为竞争风险的NLR死亡和NLR-NAR事件的调整后亚危险率(sHR)。分析的NLR-NAR事件包括糖尿病,慢性肾功能衰竭,心血管事件,NLR-NAR癌症,骨骼事件和非艾滋病相关感染。调整变量包括年龄,性别,以前的艾滋病,HIV传播类别,最低点CD4 + T细胞计数,抗逆转录病毒疗法,HIV RNA,肝纤维化,HCV基因型以及接触特定抗HIV药物毒品。在纳入的1,625名患者中,有592名(36%)持续病毒反应(SVR)。在进行了5年的中位随访后,发现SVR与糖尿病风险的显着降低有关(sHR,0.57; 95%置信区间[CI],0.35-0.93; P = 0.024),而SVR下降。慢性肾功能衰竭的危险接近显着性阈值(sHR,0.43; 95%CI,0.17-1.09; P = 0.075)。结论:我们的数据表明,在合并感染的患者中根除HCV不仅与减少死亡,HIV进展和肝相关事件的发生有关,而且与降低糖尿病和可能的慢性肾衰竭的危险有关。这些发现表明,无论纤维化分期如何,在合并感染患者中均应开具HCV治疗处方。 (肝病2017; 66:344-356)。

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