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Impact of Alcohol on the Histological and Clinical Progression of Hepatitis C Infection.

Hepatology(1998)SCI 1区

Univ Illinois

Cited 475|Views23
Abstract
In patients infected with the hepatitis C virus (HCV), 20% to 30% will progress to cirrhosis in over two to three decades. Viral and host factors that are important in the clinical and histologic progression of HCV infection are not entirely certain. It has been suggested that liver disease is worse in alcoholics infected with HCV. In the present retrospective study, we examined the effect of moderate alcohol intake on the histologic and clinical progression of HCV infection and assessed whether other variables such as gender, length of exposure, mode of exposure, HCV RNA levels, and ferritin levels also independently impacted disease progression. Liver biopsies were analyzed for the degree of fibrosis, presence of cirrhosis, and histologic activity by using the Histologic Activity Index of Knodell. Patients were divided into two groups based on whether their alcohol intake was significant or not significant. Significant alcohol intake was defined as > 40 g alcohol/day in women and > 60 g of alcohol/day in men for > 5 years. Groups were further divided based on the decades of exposure to HCV. There was no difference in the age or length of exposure to HCV in the alcohol and the alcohol-free group. HCV RNA serum levels, ferritin levels, and viral genotypes were similar in both groups. There was a two- to threefold greater risk of liver cirrhosis and decompensated liver disease in the alcohol group. Also, the rate to which subjects developed cirrhosis was faster in the alcohol group with 58% being cirrhotic by the second decade as opposed to 10% being cirrhotic in the nonalcohol group by the second decade. The histologic and clinical acceleration of liver disease was independent of the mode of exposure or sex. In summary, alcohol intake is an independent risk factor in the clinical and histologic progression of HCV infection.
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要点】:本文研究了酒精摄入对丙型肝炎病毒(HCV)感染患者病理和临床进展的影响,发现酒精摄入是HCV感染临床和病理进展的独立风险因素。

方法】:通过回顾性研究,分析患者肝活检结果,使用Knodell的病理活动指数评估纤维化程度、肝硬化情况和病理活动性。

实验】:将患者分为酒精摄入显著组和非显著组,定义标准为女性每日酒精摄入量超过40克,男性超过60克,且持续超过5年。两组在年龄、HCV暴露时长、HCV RNA血清水平、铁蛋白水平和病毒基因型方面相似。实验结果显示,酒精摄入组的肝硬化和失代偿性肝病风险增加了两到三倍,且肝硬化发展速度更快,第二个十年结束时肝硬化比例达到58%,而非酒精组仅为10%。病理和临床进展的加速与暴露方式或性别无关。