Thyroid Diseases and Hepatitis C Chronic Infection

Aless, R. Antonelli
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引用次数: 2

Abstract

More than 185 million subjects worldwide are infected by Hepatitis C virus (HCV), and about 20% of patients chronically infected with HCV progress to cirrhosis and 1-2% to hepatocarcinoma [1]. HCV chronic infection is also associated with extrahepatic manifestations in up to 74% of patients (mixed cryoglobulinemia, lymphomas, rheumatic disorders, type 2 diabetes, and thyroid disorders) [2]. For about two decades combination therapy with PEGylated-interferon-α [3] and ribavirin has been the standard of care for patients with HCV chronic infection; however, interferon had limited effectiveness and was associated with important adverse side effects. More recently, advances in understanding the molecular pathways associated with HCV life cycle, and the complex inflammatory network involving cytokines and chemokines associated with HCV chronic hepatitis, have led to important advancements in therapy [4]. In the last years, direct-acting antivirals (DAAs) (as protease inhibitors, polymerase inhibitors, or NS5A inhibitors) have been used to treat HCV chronic infection, resulting in shorter treatment duration, better efficacy and tolerance, and are able to eradicate HCV [5,6].
甲状腺疾病和慢性丙型肝炎感染
全世界有超过1.85亿人感染丙型肝炎病毒(HCV),约20%的慢性丙型肝炎病毒感染患者发展为肝硬化,1-2%发展为肝癌。在高达74%的患者(混合性冷球蛋白血症、淋巴瘤、风湿性疾病、2型糖尿病和甲状腺疾病)中,HCV慢性感染也与肝外表现相关。二十年来,聚乙二醇干扰素-α[3]和利巴韦林联合治疗一直是HCV慢性感染患者的标准治疗方案;然而,干扰素的有效性有限,并伴有严重的副作用。最近,在了解与HCV生命周期相关的分子途径以及与HCV慢性肝炎相关的细胞因子和趋化因子的复杂炎症网络方面的进展,导致了治疗bbb的重要进展。近年来,直接作用抗病毒药物(DAAs)(如蛋白酶抑制剂、聚合酶抑制剂或NS5A抑制剂)已被用于治疗HCV慢性感染,治疗时间更短,疗效更好,耐受性更好,并且能够根除HCV[5,6]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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