Institut de Veille Sanitaire, Saint-Maurice, France.
J Med Virol. 2010 Oct;82(10):1647-54. doi: 10.1002/jmv.21850.
Although risk factors for cirrhosis in chronic hepatitis C virus (HCV) infection have been identified, the role of HCV-genotype 3 remains controversial, and limited data are available in drug users. The aim of the study was to assess risk factors for severe liver disease (cirrhosis/hepatocellular carcinoma) in HCV-infected drug users between 2001 and 2007 in France. Patients who reported drug use and who had been referred for HCV infection to hepatology centers from a national surveillance system were identified. The severity of liver disease was assessed clinically and histologically (Metavir score). Factors associated with severe liver disease were analyzed after estimating missing values by multiple imputation (MI). Of the 4,065 drug users naive to anti-HCV treatment who were referred to the 26 participating centers, 8.0% had severe liver disease, 25.7% were infected with HCV-genotype 3. Factors associated independently with an increased risk of severe liver disease were HCV-genotype 3 (adjusted odds ratio, multiple imputation (aOR(MI)) = 1.6, [95% confidence interval, 95% CI: 1.2-2.1]), HIV infection (aOR(MI) = 1.8, [1.2-2.8]), male sex (aOR(MI) = 2.0, [1.4-2.8]), age over 40 years (aOR(MI) = 2.1, [1.6-2.9]), history of excessive alcohol consumption (aOR(MI) = 2.8, [2.1-3.7]), and duration of infection ≥18 years (aOR(MI) = 2.9, [2.0-4.3]). This analysis shows that HCV-genotype 3 is associated with severe liver disease in drug users, independently of age, sex, duration of infection, alcohol consumption, and co-infection with HIV. These results are in favor of earlier treatment for drug users infected with HCV- genotype 3 and confirm the need for concomitant care for excessive alcohol consumption.
尽管已经确定了慢性丙型肝炎病毒 (HCV) 感染导致肝硬化的危险因素,但 HCV 基因型 3 的作用仍存在争议,且在吸毒者中可用的数据有限。本研究旨在评估 2001 年至 2007 年期间法国 HCV 感染吸毒者发生严重肝脏疾病(肝硬化/肝细胞癌)的危险因素。从国家监测系统中报告吸毒且被转介至肝病中心的患者被确定为研究对象。通过多变量插补(MI)估计缺失值后,评估肝脏疾病的严重程度。在临床和组织学上(Metavir 评分)评估了严重肝脏疾病。采用多变量插补(MI)分析与严重肝脏疾病相关的因素。在被转介至 26 个参与中心的 4065 名初治抗 HCV 治疗的吸毒者中,8.0%患有严重肝脏疾病,25.7%感染 HCV 基因型 3。与严重肝脏疾病风险增加独立相关的因素包括 HCV 基因型 3(调整后比值比,多变量插补(MI)(aOR(MI))=1.6,95%置信区间,95%CI:1.2-2.1)、HIV 感染(aOR(MI)=1.8,[1.2-2.8])、男性(aOR(MI)=2.0,[1.4-2.8])、年龄>40 岁(aOR(MI)=2.1,[1.6-2.9])、过量饮酒史(aOR(MI)=2.8,[2.1-3.7])和感染时间≥18 年(aOR(MI)=2.9,[2.0-4.3])。该分析表明,HCV 基因型 3 与吸毒者的严重肝脏疾病独立相关,与年龄、性别、感染持续时间、饮酒和 HIV 合并感染无关。这些结果支持对感染 HCV 基因型 3 的吸毒者进行早期治疗,并证实需要同时治疗过量饮酒。