首页> 中文期刊> 《浙江医学》 >金华地区慢性乙型肝炎患者HBV基因型及耐药基因位点突变类型分析

金华地区慢性乙型肝炎患者HBV基因型及耐药基因位点突变类型分析

         

摘要

目的 分析金华地区慢性乙型肝炎患者HBV基因型分布特征及HBV耐药基因位点突变情况,并探讨两者的关系.方法 选取1 04例经核苷(酸)类似物治疗的慢性乙型肝炎患者为研究对象,采用Sanger双脱氧法测序技术检测患者血清HBV的基因型和10种常见的HBV P区耐药基因位点突变情况,并分析两者关系.结果 本组慢性乙型肝炎患者中,HBV B基因型占46.15%,C基因型占53.85%,未发现其他基因型.检测出发生耐药基因位点突变61例,突变率为58.65%,其中C基因型占65.57%,B基因型占34.43%.HBV P区耐药基因位点突变率最高的为M204V/I(73.85%),其次为L180M(36.92%)和A181V/T(23.08%).HBV P区耐药基因发生单位点突变的占50.82%,其中M204I突变类型最多(29.51%);发生多位点突变的占49.18%;以M204I和M204V/I“180M两种突变类型最常见.HBV C基因型的患者耐药基因突变率高于B基因型的患者(71.43% vs 43.75%,P<0.05),其中C基因型的患者A181V/T位点突变率高于B基因型的患者(14.29% vs 2.08%,P<0.05).结论 金华地区慢性乙型肝炎患者HBV基因型以B、C基因型为主;HBV P区耐药基因位点突变类型以M204I和M204V/I+L180M两种类型最常见;HBV C基因型的患者比B基因型的患者更易发生耐药突变,且更易发生A181V/T位点突变.%Objective To analyze genotypes and mutation patterns of HBV gene in chronic hepatitis B patients in Jinhua.Methods One hundred and four patients with chronic hepatitis B who were treated with nucleoside analogues,were enrolled in the study.Sanger sequence analysis of HBV genotypes and 10 common sites of HBV P region were performed.Results There were 46.15% cases of B genotype and 53.85% of C genotype among 104 chronic hepatitis B patients.Other genotypes were no detected.HBV P gene mutation were detected in 61 cases (58.65%);there was 65.57% in HBV C genotype and 34.43% in B genotype.M204V/I was the most common site of HBV P gene mutation (73.85%),followed by L180M (36.92%) and A181V/T (23.08%).50.82% cases had single site mutation and the most mutation pattern was M204I (29.51%);and 49.18% had multiple sites mutation;the most common mutation patterns were M204I and M204V/I+L180M.The resistance mutation rate in C genotype was higher than that in B genotype(71.43% vs 43.75%,P<0.05) and the mutation rate of A181V/T in C genotype cases was higher than that in B genotype cases (14.29% vs 2.08%,P<0.05).Conclusion Genotype B and C are the main genotypes of HBV in this study.The most common mutation patterns of HBV P gene were M204I and M204V/I+L180M.Genotype C patients had more mutations than genotype B and the A181V/T mutation pattern was more common in genotype C.

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