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丙型肝炎病毒准种的多样性程度与肝脏疾病的进展

Degree of diversity of hepatitis C virus quasispecies and progression of liver disease.

作者信息

Honda M, Kaneko S, Sakai A, Unoura M, Murakami S, Kobayashi K

机构信息

First Department of Internal Medicine, Kanazawa University, Japan.

出版信息

Hepatology. 1994 Nov;20(5):1144-51.

PMID:7927245
Abstract

We examined the quasispecies of the hepatitis C virus genome in 28 patients with liver disease of varying severity. Nucleotide sequences of the hepatitis C virus genome spanning the region from the core to envelope were used to calculate the nucleotide diversity: 0.58% +/- 0.88% in 5 patients with acute hepatitis, 0.85% +/- 0.62% in 5 patients with chronic persistent hepatitis, 1.79% +/- 0.92% in 11 patients with chronic active hepatitis, 3.05% +/- 1.26% in 4 patients with cirrhosis and 2.71% +/- 1.47% in 3 patients with cirrhosis complicated by hepatocellular carcinoma. Thus the intrapatient variation in nucleotides increased significantly with severity of liver disease (p < 0.01), except in those cases of cirrhosis complicated by hepatocellular carcinoma. Multivariate analysis including the histology, duration of infection, age, sex, history of blood transfusion and serum level of ALT at diagnosis as variables showed that the histological finding was the strongest independent factor of the nucleotide diversity (p = 0.003). Serial analysis of the genome in three patients demonstrated that the intra-patient variation in nucleotides increased with the progression of liver disease. The magnitude of the intrapatient variation in nucleotides deduced from the observed changes in the patients was correlated with the mean serum levels of ALT. These findings suggest that the degree of diversity of HCV quasispecies is related to the progression of liver disease.

摘要

我们检测了28例不同严重程度肝病患者丙型肝炎病毒基因组的准种。采用丙型肝炎病毒基因组从核心区到包膜区的核苷酸序列计算核苷酸多样性:5例急性肝炎患者为0.58%±0.88%,5例慢性持续性肝炎患者为0.85%±0.62%,11例慢性活动性肝炎患者为1.79%±0.92%,4例肝硬化患者为3.05%±1.26%,3例合并肝细胞癌的肝硬化患者为2.71%±1.47%。因此,除合并肝细胞癌的肝硬化病例外,患者体内核苷酸变异随肝病严重程度显著增加(p<0.01)。将组织学、感染持续时间、年龄、性别、输血史及诊断时血清ALT水平作为变量进行多因素分析,结果显示组织学表现是核苷酸多样性的最强独立因素(p = 0.003)。对3例患者的基因组进行序列分析表明,患者体内核苷酸变异随肝病进展而增加。根据患者观察到的变化推断的患者体内核苷酸变异程度与ALT平均血清水平相关。这些发现提示丙型肝炎病毒准种的多样性程度与肝病进展有关。

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