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Baseline Amino Acid Substitutions in the NS5A ISDR and PKR Binding Domain of Hepatitis C and Different Fibrosis Levels and Levels of Development of Hepatocellular Carcinoma in Patients Treated with DAAs

机译:DAA治疗的丙型肝炎的NS5A ISDR和PKR结合域中的基线氨基酸取代以及不同的纤维化水平和肝细胞癌的发展水平

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摘要

Variations in the interferon sensitivity-determining region (ISDR) within the NS5A region were related to the development of hepatocellular carcinoma (HCC) in patients infected with hepatitis C virus (HCV). The aim of the study was to investigate a relationship between ISDR/PKR substitutions and their association with liver fibrosis or HCC development. A total of 316 patients infected with HCV and treated with DAAs were evaluated. HCV RNA was quantified and sequenced before treatment. The liver fibrosis stage was assessed by transient elastography and equalized to METAVIR scores. Multivariate analysis showed that ≥3 substitutions in ISDR and ≥6 in PKR-bd were significantly associated with advanced fibrosis. Advanced fibrosis was observed in patients with higher substitutions in ISDR and PKR-bd. A higher correlation between advanced fibrosis and a high frequency of ≥3 substitutions in ISDR and ≥6 in PKR-bd was observed in patients infected with genotype 2c. In addition, in a higher proportion of HCC patients, advanced fibrosis (40.4% vs. 88.2%; < 0.001) and ≥6 substitutions in PKR-bd (15.4% vs. 41.2%; = 0.01) was observed. In conclusion, a higher number of substitutions in ISDR and PKR-bd were associated with advanced liver fibrosis, suggesting a use of like predictors for progression in the liver damage. A significantly higher number of PKR-bd substitutions was observed in HCC patients; in particular, in patients infected with HCV genotype 2c.
机译:NS5A区域内干扰素敏感性决定区(ISDR)的变化与感染丙型肝炎病毒(HCV)的患者肝细胞癌(HCC)的发生有关。这项研究的目的是调查ISDR / PKR替代与肝纤维化或HCC形成之间的关系。总共评估了316例HCV感染和DAA治疗的患者。治疗前对HCV RNA进行定量和测序。通过瞬时弹性成像评估肝纤维化阶段,并等于METAVIR评分。多变量分析表明,ISDR≥3取代和PKR-bd≥6与晚期纤维化显着相关。在ISDR和PKR-bd替代较高的患者中观察到晚期纤维化。在基因型2c感染的患者中,观察到晚期纤维化与ISDR≥3的高频率替代和PKR-bd≥6的高频率相关。此外,在较高比例的肝癌患者中,观察到晚期纤维化(40.4%比88.2%; <0.001)和PKR-bd≥6替代(15.4%比41.2%; = 0.01)。总而言之,ISDR和PKR-bd中更多的取代与晚期肝纤维化有关,表明使用类似的预测因子来预测肝损伤的进展。在HCC患者中观察到大量的PKR-bd替代;特别是在感染HCV基因型2c的患者中。

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