[HBV genotype and liver histology effect of peginterferon alpha treatment of HBeAg-position chronic hepatitis B].

中华实验和临床病毒学杂志 Pub Date : 2013-06-01
Chuan-Tong Lu, Guo-Sheng Gao, Hua-Dong Yan, Yao-Ren Hu
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Abstract

Objective: To investigate the efficacy of PEG-interferon alpha (PEG-IFN alpha) treatment of HBeAg-positive chronic hepatitis B and HBV genotypes and liver tissues effect of HBeAg seroconversion.

Methods: 54 cases confirmed by liver biopsy, genotype clear HBeAg positive chronic hepatitis B (CHB) patients according to body weight, respectively, subcutaneous injection of PEG-IFN-alpha2a 135 microg or 180 microg, or PEG-IFN-alpha2b 50 microg, 80 microg or 100 microg once weekly treatment for 48 weeks and followed for 24 weeks after discontinuation. Statistics of HBeAg seroconvertion, HBV genoty pes and liver histology e antigen seroconversion after the end of treatment.

Results: 54 patients were followed up at the end of HBeAg seroconversion rate was 29.63% (16/54). Genotype B patients with HBeAg seroconversion rate was 35.29%, 27.03% higher than the C-type patients, but the difference was not statistically significant (chi2 = 0.382, P = 0.537). Inflammation of the liver activity highter ( > G2) , the degree of fibrosis heavier ( > S1) HBeAg seroconversion rate (50.00% vs. 25.00%, 40.90% vs. 21.88%), but were not statistically significant (chi2 = 1.391, 1.444, P = 0.238, 0.229). Activity of HBV genotype, liver inflammation, liver fibrosis and other factors by multivariate Logistic regression analysis, only liver inflammation activity of the important factors of HBeAg seroconversion.

Conclusion: Important factors, liver inflammation activity of PEG-interferon alpha treatment of HBeAg-position chronic hepatitis B patients and HBV genotypes and liver fibrosis may be of little significance.

[聚乙二醇干扰素α治疗hbeag位点慢性乙型肝炎的HBV基因型和肝脏组织学影响]。
目的:探讨聚乙二醇-干扰素α (PEG-IFN α)治疗HBeAg阳性慢性乙型肝炎和HBV基因型的疗效及HBeAg血清转化对肝组织的影响。方法:54例经肝活检证实,基因型明确HBeAg阳性的慢性乙型肝炎(CHB)患者根据体重,分别皮下注射PEG-IFN-alpha2a 135 μ g或180 μ g,或PEG-IFN-alpha2b 50 μ g、80 μ g或100 μ g,每周1次治疗48周,停药后随访24周。治疗结束后HBeAg血清转化、HBV基因型及肝脏组织学e抗原血清转化的统计。结果:54例患者随访结束时HBeAg血清转化率为29.63%(16/54)。基因型B患者HBeAg血清转化率为35.29%,比c型患者高27.03%,但差异无统计学意义(χ 2 = 0.382, P = 0.537)。肝脏炎症活动度较高(> G2),纤维化程度较重(> S1), HBeAg血清转化率(50.00% vs. 25.00%, 40.90% vs. 21.88%),但差异无统计学意义(χ 2 = 1.391, 1.444, P = 0.238, 0.229)。HBV基因型活性、肝脏炎症、肝纤维化等因素经多因素Logistic回归分析,只有肝脏炎症活性是影响HBeAg血清转化的重要因素。结论:肝炎症活性的重要因素peg -干扰素α治疗hbeag位点慢性乙型肝炎患者与HBV基因型及肝纤维化的关系可能意义不大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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