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[慢性丙型肝炎:轻度疾病患者]

[Chronic hepatitis C: patients with mild disease].

作者信息

Quer Juan Carlos, Diago Moisés, Crespo Javier, García-Samaniego Javier, Morillas Rosa, Andrade Raúl, Ángel Simón Miguel

机构信息

Servicio de Aparato Digestivo, Hospital Universitario Joan XXIII, Tarragona, España.

Servicio de Aparato Digestivo, Hospital General, Valencia, España.

出版信息

Gastroenterol Hepatol. 2014 Jul;37 Suppl 1:3-12. doi: 10.1016/S0210-5705(15)30002-9.

Abstract

Chronic hepatitis C virus infection is usually asymptomatic. The severity of the hepatic lesion in these patients at diagnosis varies and, from the histopathologic point of view, most have mild disease. A series of factors have been described that correlate with the progression of fibrosis in patients with mild fibrosis: age at diagnosis, the duration of the infection, male sex, HIV coinfection, transaminase levels during follow-up, alcohol consumption, metabolic factors such as diabetes and overweight, necroinflammatory activity in the initial biopsy, and the degree of steatosis. In patients with genotype 1 hepatitis C infection, the standard treatment has been pegylated interferon and ribavirin. However, response rates are markedly increased by concomitant use of first-generation protease inhibitors, boceprevir or telaprevir. In patients with moderate fibrosis, these drugs are well tolerated, in addition to being effective. Currently, dual therapy should be reserved for patients with good baseline predictive factors of response and/or contraindications for treatment with telaprevir or boceprevir. In patients with genotypes other than genotype 1, the standard treatment continues to be the combination of pegylated interferon and ribavirin, although the development of new direct-acting antiviral agents such as sofosbuvir and simeprevir will change the strategies used in these patients. The decision to wait for the new treatments is complex because their release date is unknown; likewise, their high cost will limit the possibilities for their use.

摘要

慢性丙型肝炎病毒感染通常无症状。这些患者在诊断时肝脏病变的严重程度各不相同,从组织病理学角度来看,大多数患者病情较轻。已描述了一系列与轻度纤维化患者纤维化进展相关的因素:诊断时的年龄、感染持续时间、男性、合并感染HIV、随访期间的转氨酶水平、饮酒量、糖尿病和超重等代谢因素、初次活检时的坏死性炎症活动以及脂肪变性程度。对于基因型1丙型肝炎感染患者,标准治疗方法一直是聚乙二醇化干扰素和利巴韦林。然而,同时使用第一代蛋白酶抑制剂博赛匹韦或特拉匹韦可显著提高应答率。对于中度纤维化患者,这些药物耐受性良好,且疗效显著。目前,双联疗法应仅用于具有良好基线应答预测因素和/或有使用特拉匹韦或博赛匹韦治疗禁忌证的患者。对于基因型1以外的其他基因型患者,标准治疗仍然是聚乙二醇化干扰素和利巴韦林联合使用,尽管索磷布韦和西米普明等新型直接抗病毒药物的出现将改变这些患者的治疗策略。等待新疗法的决定很复杂,因为其发布日期未知;同样,其高昂的成本也将限制其使用可能性。

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