Gao Guo-sheng, Xu Xiao-zhen, Hu Yao-ren, Yan Hua-dong
Liver Diseases Branch of Ningbo No.2 Hospital,Ningbo 315010, China. Email:
Zhonghua Nei Ke Za Zhi. 2013 Dec;52(12):1009-12.
To investigate the efficacy of polyethylene glycol (PEG)-interferon α (PEG-IFNα) in treating HBeAg-positive chronic hepatitis B (CHB) and explore the relationship between hepatitis B virus (HBV) genotypes and the effect of interferon α (IFNα) therapy.
A total of 199 CHB patients with known genotypes were given subcutaneous injection of PEG-IFNα-2a or PEG-IFNα-2b once a week for 48 weeks, with another 24 weeks follow up. The seroconversion of HBeAg influenced by HBV genotypes were analyzed after discontinuation of treatment.
In local area, genotype C was the major genotype [64.32% (128/199) ]. Except serum ALT and AST level, the differences in gender, age, liver inflammation, degree of liver fibrosis, HBeAg level and HBV DNA level between genotype B and C were not statistically significant (all P > 0.05). The seroconversion rate of HBeAg in patients with genotype B at early stage of therapy (3 months) was significantly higher than that of patients with genotype C [26.76% (19/71) vs 10.16% (13/128), χ(2) = 9.330, P = 0.002]. While at the end of follow-up, seroconversion rate of HBeAg in patients with genotype B (followed up for 6 months) was higher than that of patients with genotype C [39.44% (28/71) vs 30.47% (39/128)], but the difference was not statistically significant (χ(2) = 1.645, P = 0.200). By univariate analysis based on log-rank test, the time of HBeAg seroconversion in patients with genotype B was much earlier than that of genotype C [(13.99 ± 0.67) months vs (15.47 ± 0.41) months], but the difference was not statistically significant (P = 0.150).
The seroconversion rate of HBeAg in patients with genotype B treated with PEG-IFNα was significantly higher than that of genotype C in early stage of therapy (3 months), while similar at the end of therapy.
探讨聚乙二醇(PEG)干扰素α(PEG-IFNα)治疗HBeAg阳性慢性乙型肝炎(CHB)的疗效,并探讨乙型肝炎病毒(HBV)基因型与干扰素α(IFNα)治疗效果之间的关系。
对199例已知基因型的CHB患者皮下注射PEG-IFNα-2a或PEG-IFNα-2b,每周1次,共48周,随后进行24周随访。停药后分析受HBV基因型影响的HBeAg血清学转换情况。
在本地区,C基因型是主要基因型[64.32%(128/199)]。除血清ALT和AST水平外,B基因型和C基因型患者在性别、年龄、肝脏炎症、肝纤维化程度、HBeAg水平和HBV DNA水平方面的差异无统计学意义(均P>0.05)。治疗早期(3个月)B基因型患者的HBeAg血清学转换率显著高于C基因型患者[26.76%(19/71)对10.16%(13/128),χ(2)=9.330,P=0.002]。而在随访结束时,B基因型患者(随访6个月)的HBeAg血清学转换率高于C基因型患者[39.44%(28/71)对30.47%(39/128)],但差异无统计学意义(χ(2)=1.645,P=0.200)。基于对数秩检验的单因素分析显示,B基因型患者的HBeAg血清学转换时间早于C基因型患者[(13.99±0.67)个月对(15.47±0.41)个月],但差异无统计学意义(P=0.150)。
PEG-IFNα治疗的B基因型患者在治疗早期(3个月)的HBeAg血清学转换率显著高于C基因型患者,而在治疗结束时相似。