肝脏疾病进展与乙型肝炎病毒前 C/C 区突变  被引量:3

Clinical significance of hepatitis B virus (HBV) precore and core promoter mutations affecting HBV e-antigen expression and their association with liver disease progression

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作  者:付丽娟[1] 陈颖[1] 张怡[2] 滕旭[3] 张亚男[1] 杨志伟[1] 

机构地区:[1]黑龙江省医院感染内科,哈尔滨150036 [2]黑龙江省中医药大学附属第一医院 [3]哈尔滨医科大学微生物教研室

出  处:《中国医师杂志》2014年第6期721-723,共3页Journal of Chinese Physician

基  金:国家自然科学基金青年科学基金(31100077);黑龙江省卫生厅课题(2006435)

摘  要:目的:研究慢性乙型肝炎患者前C/C区突变位点与肝脏疾病进展的临床意义。方法应用实时荧光定量PCR及直接测序法检测HBeAg阴性慢性乙型肝炎30例、HBeAg阳性慢性乙型肝炎20例,分析前C/C区变异位点与患者病情进展的相关性。结果肝硬化组前C/C区变异位点T1762/A1764、A1896发生率(86.3%,54.5%)明显高于慢性肝炎组(32.1%,35.7%),差异均有统计学意义( P <0.05)。慢性肝炎组与肝硬化组HBV载量差异无统计学意义( P >0.05);HBeAg阴性患者T1762/A1764,T1766/A1768,A1896变异位点发生率较HBeAg阳性患者显著增高( P <0.05)。结论 T1762/A1764,A1896突变率的增加会促使肝脏疾病进展至肝硬化;HBeAg阴患者T1762/A1764,T1766/A1768,A1896变异位点的频率增加会促进肝脏疾病的进展。Objective To investigate the association of hepatitis B virus ( HBV) precore ( preC) /C mutations with the pro-gression of liver disease .Methods The HBV genes of 50 chronic hepatitis B , including 30 HBV e-antigen ( HBeAg)-negative and 20 HBeAg-positive patients, were detected with real-time quantification polymerase chain reaction (RT-PCR) and the direct sequencing method.Results The mutations T1762/A176, T1766/A1768, A1896 , and the levels of HBV viral loads significantly correlated with the disease progression .The HBeAg-negative patients had a higher frequency of mutations at T 1762/A1764 , T1766/A1768 , and A 1896 relative to HBeAg-positive patients .Conclusions Patients with advanced liver diseases and with HBeAg-negativity possibly had multi-mutations at T1762/A1764, T1766/A1768, and A1896 in HBV genomes.

关 键 词:肝炎病毒 乙型 遗传学 点突变 肝疾病 

分 类 号:R512.62[医药卫生—内科学]

 

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