摘要
目的调查广州地区乙型肝炎病毒(HBV)基因亚型分布情况,并探讨其与HBV感染疾病谱的关系。方法采用直接测序法测定S基因序列并构建基于S基因进化树,对424例HBV感染者进行研究,随机选择慢性乙型肝炎(CHB)137例,HBV相关慢加急性肝衰竭(HB-ACLF)90例,肝硬化(LC)90例和肝细胞癌(HCC)107例,应用SPSS 13.0软件进行x^2检验、方差分析和多元Logistic回归分析。结果在424例HBV感染者中,B2亚型269例(63.44%),C1亚型117例(27.59%),C2亚型36例(8.49%),C5亚型2例(0.47%),未发现其他亚型;CHB患者感染HBV B2亚型、C1亚型、C2亚型和C5亚型分别为70.1%、24.09%、5.11%和0.73%;HB-ACLF患者感染HBV B2亚型、C1亚型和C2亚型分别为87.78%、7.78%、4.44%,其中HBV B2基因亚型显著高于CHB(x^2=9.641,P=0.002)、LC(x^2=19.565,P=0.000)、HCC患者(x^2=26.789,P=0.000);LC患者感染HBV B2亚型、C1亚型和C2亚型分别为50.00%、36.67%、13.33%,其中HBV C1和C2亚型显著高于CHB患者(x^2=6.262,P=0.012;x^2=4.790,P=0.029)或HB-ACLF患者(x^2=25.894,P=0.000;x^2=4.390,P=0.036);HCC患者感染HBV B2亚型、C1亚型、C2亚型和C5亚型分别为45.79%、41.12%、12.15%、0.93%,其中HBV C1和C2亚型也显著高于CHB患者(x^2=11.264,P=0.001;x^2=3.957,P=0.047)或HB-ACLF患者(x^2=28.327,P=0.000;x^2=3.904,P=0.048);LC和HCC患者HBV C1和C2基因亚型无明显差异(x^2=0.429,P=0.512;x^2=0.804,P=0.833);多因素Logistic回归分析提示B2亚型是HB-ACLF发生的危险因素(OR=2.597,95%CI=1.145~5.891,P=0.022),C型是HCC发生的危险因素(OR=3.257,95%CI=1.49~7.194,P=0.003)。结论广州地区HBV基因亚型主要由B2、C1和C2亚型构成,同时也存在C5亚型;广州地区B2亚型感染者可能更易发生HBV相关慢加急性肝衰竭,而C1和C2亚型感染者可能更易进展为肝硬化和肝细胞癌。
Objective To investigate hepatitis B virus (HBV) subgenotypes distribution and its implication in patients with chronic hepatitis B in Guangzhou. Methods 424 patients were enrolled in this study,including 137 with chronic hepatitis B (CHB),90 with HBV-related acute-on-chronic liver failure (HB-ACLF),90 with 1iver cirrhosis (LC) and 107 with hepatocellular carcinoma (HCC). HBV subgenotypes were determined by direct sequencing of HBV S gene and the phylogenetic tree was constructed. The data was compared by x2 test,one way ANOVA and Logistic regression analysis. Results Out of 424 patients with HBV infection, 269 (63.44%) were infected with HBV B2,117 (27.59% with HBV C1,36 (8.49%) with HBV C2 and 2 (0.47%) with C5; the HBV B2,C1,C2 and C5 Infection in patients with CHB were 70.1%,24.09%,5.11%,0.73%;the HBV B2,C1 and C2 in patients with HB-ACLF were 87.78%,7.78%,4.44%,with HBV B2 subgenotpe significantly higher than in patients with CHB(x2=9.641,P=0.002),with LC(x2=19.565,P=0.000) or with HCC (x2=26.789,P =0.000);the subgenotypes of HBV B2,C1 and C2 in patients with LC were 50.00%,36.67%,13.33%,with HBV C1 and C2 subgenotpes significantly higher than in patients with CHB(x2=6.262,P=0.012,x2=4.790,P=0.029) or in patients with HB-ACLF(x2=25.894 P=0.000,x2=4.390, P=0.036);the subgenotypes of HBV B2,C1,C2 and C5 in HCC patients were 45.79%,41.12%,12.15%,0.93,with HBV C1 and C2 subgenotypes significantly higher than in patients with CHB (x2=11.264,P=0.001,x2=3.957,P=0.047) or in patients with HB-ACLF (x2=28.327,P=0.000,x2=3.904,P=0.048);there was no significant difference between HCC patients with HBV C1 and C2 subgenotype infection and LC patients;Logistic regression analysis showed that HBV B2 subgenotype was the independent risk factor for HB-ACLF occurrence, and HBV C genotype was the independent risk factor for HCC occurrence. Conclusion HBV B2,C1,C2 are the most frequent HBV subgenotypes in Guangzhou. The HBV B2 subgenotpe is prevalent in patients with HB-ACLF and HBV C1 and C2 is frequent in patients with LC and HCC.
出处
《实用肝脏病杂志》
CAS
2016年第5期528-531,共4页
Journal of Practical Hepatology
基金
广州市科技计划项目(编号:2014Y2-00079)