乙型肝炎病毒基因型对乙型肝炎病毒变异的影响  

Effect of hepatitis B virus genotypes on mutations of hepatitis B virus precore and basic core promotor

作　　者：肖扬[1] 朱冰星[1] 周岳进[1] 张文静[1] 胡侠[1] 胡操寒[1] 谢庆荣[1] 王开鉴[1] 

机构地区：[1]浙江温州解放军第一一八医院肝病科,325000

出　　处：《肝脏》2006年第2期89-91,共3页Chinese Hepatology

摘　　要：目的探讨乙型肝炎病毒(HBV)基因型对病毒前核心区(前C区,nt1896)及基本核心启动子(BCP,nt1762/1764)变异的影响。方法416例血清HBsAg阳性、HBVDNA定量大于1.0×104拷贝/ml的患者,采用微流基因芯片检测HBV基因型、前C区及BCP变异。结果416例HBV感染者中406例有基因分型结果:B型20.9%、C型65.9%、BC混合型10.8%,10例患者未分出基因型。302例为HBeAg(-)且HBVDNA(+)患者,其中248例(82.12%)有前C区或BCP变异,41.06%为前C区变异,31.12%BCP变异,2种同时变异为9.94%。B型患者前C区变异率为22.9%(20/87),与C型患者前C区变异率39.4%(108/274)及B、C混合型变异率40.0%相比均有显著差异(P<0.01)。在BCP变异及双变异,C型患者变异率均大于B型患者,但差异无统计学意义(P>0.05)。B、C混合型患者前C区及BCP变异率与C型相似。结论HBV基因型可影响病毒前C区及BCP变异,以C型为著。Objective % study the effect of hepatitis B virus（HBV） genotypes on mutations of HBV precore and basic core promotor （BCP）. Methods Serum samples of 416 patients with chronic hepatitis B（CHB） were determined for precore and BCP mutations by microfluidic chip. Results Among frona 416 cases, tile genotype of HBV have been determined in 406 cases. The rate of genotype B was 20.9%, genotype C was 65.9%, B and C mix-type was 10.8%, 10 patients＇ s genotypes were not identified. Among 302 HBeAg negative cases, 248 （82.12% ）had mutations of preeore or/and BCP, The rates of cases with precore tnutant BCP mutant and double mutant were 41.06% ,31.02% and 9.94%, respectively. The rate of precore mutant in the patients with genotype B was 22.9 %, which was significant dittbrence （ P 〈 0.01 ）eornpared with that in patients with genotype C or B and C mix-type（39.4% and 40.0% ,lespectively）. The rates of BCP mutant arut two mutants in patients with genotype C were. higher than those in patients with genotype B, but no significantly different （ P 〉 0.05）. The rates of preeore and/or BCP mutants in patients with B and C mix-type were similar to that in patients with genotype C. Conclusion Hepatitis B virus genotypes may have effect on mutations of precore and/or BCP,especially genotype C.

关 键 词：乙型肝炎病毒 基因型 前核心区 基本核心启动子 变异 

分 类 号：R512.62[医药卫生—内科学] R373.21[医药卫生—临床医学]