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乙型肝炎X基因区域的突变:慢性乙型肝炎与肝硬化

Mutations in Hepatitis-B X-Gene Region: Chronic Hepatitis-B versus Cirrhosis.

作者信息

Salarnia Farzaneh, Besharat Sima, Zhand Sare, Javid Naeme, Khodabakhshi Behnaz, Moradi Abdolvahab

机构信息

Researcher, Infectious Disease Research Center, Golestan University of Medical Sciences, Gorgan, Golestan, Iran.

Assistant Professor, PhD, Golestan Research Center of Gastroentrology and Hepatology, Golestan University of Medical Sciences, Gorgan, Golestan, Iran.

出版信息

J Clin Diagn Res. 2017 Mar;11(3):OC31-OC34. doi: 10.7860/JCDR/2017/22570.9498. Epub 2017 Mar 1.

Abstract

INTRODUCTION

Specific mutations in Hepatitis-B Virus (HBV) genome would proceed the development of chronic hepatitis B to more serious consequences like cirrhosis and end-stage liver disease.

AIM

This study was designed to detect deletion and insertion mutational patterns in the X-gene region in a population of chronic HBV and related cirrhosis patients.

MATERIALS AND METHODS

Sixty eight chronic HBV patients and 34 HBV-related cirrhotics were recruited from the eligible cases (N=50) referred to the academic hospitals of Gorgan city, Northeast of Iran, between Jan 2011 to Dec 2013. The HBx region was amplified by semi-nested PCR using serum samples and analyzed by sequencing.

RESULTS

Our findings showed deletions and insertions in the C-terminal of HBx of the cirrhotic group and 8 bp found in two chronic HBV cases (2.9%). We detected 15 types of deletions in cirrhotic cases such as 1762-1768, 1763-1770, 1769-1773 and T1771/A1775.

CONCLUSION

We found that the frequencies of deletion and insertion mutations in C-terminal of X-gene were more seen in cirrhotic patients comparing to chronic HBV cases in our area of study.

摘要

引言

乙型肝炎病毒(HBV)基因组中的特定突变会使慢性乙型肝炎发展为更严重的后果,如肝硬化和终末期肝病。

目的

本研究旨在检测慢性HBV患者及相关肝硬化患者群体中X基因区域的缺失和插入突变模式。

材料与方法

2011年1月至2013年12月期间,从伊朗东北部戈尔甘市学术医院转诊的符合条件的病例(N = 50)中招募了68例慢性HBV患者和34例HBV相关肝硬化患者。使用血清样本通过半巢式PCR扩增HBx区域,并进行测序分析。

结果

我们的研究结果显示,肝硬化组HBx的C末端存在缺失和插入,在两例慢性HBV病例(2.9%)中发现了8个碱基对的插入。我们在肝硬化病例中检测到15种类型的缺失,如1762 - 1768、1763 - 1770、1769 - 1773和T1771/A1775。

结论

我们发现,在我们的研究区域,与慢性HBV病例相比,肝硬化患者中X基因C末端的缺失和插入突变频率更高。

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[Associations between hepatitis B virus x gene mutations and hepatocellular carcinoma].[乙型肝炎病毒X基因变异与肝细胞癌之间的关联]
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