干扰素β启动子刺激因子1基因多态性与HBeAg阳性慢性乙型肝炎患者聚乙二醇干扰素α治疗应答的关系

吴海清; 赵钢德; 李凤棣; 刘柯慧; 徐玉敏; 林兰意; 谢青; 王晖

doi:10.3969/j.issn.1001-5256.2014.08.015

干扰素β启动子刺激因子1基因多态性与HBeAg阳性慢性乙型肝炎患者聚乙二醇干扰素α治疗应答的关系

DOI: 10.3969/j.issn.1001-5256.2014.08.015

1. 上海交通大学医学院附属瑞金医院感染科
2. 上海交通大学附属上海市第一人民医院心内科

基金项目:

国家自然科学基金(81070334)；上海市科学技术委员会科技支撑项目(13401902900)；上海市公共卫生优秀学科带头人培养计划(GWDTR201202)；十二五“艾滋病和病毒性肝炎等重大传染病防治”科技重大专项课题(2012ZX10005004-002)；上海市卫生和计划生育委员会重点课题(20134004)；

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中图分类号: R512.62
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出版历程
- 收稿日期: 2013-10-09
- 出版日期: 2014-08-20

Association between IPS- 1 polymorphisms and PEG- IFN treatment response in patients with HBeAg- positive chronic hepatitis B

Department of Infectious Diseases, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University

Research funding:

摘要

摘要: 目的探讨干扰素β启动子刺激因子（IPS）-1基因多态性与HBeAg阳性慢性乙型肝炎患者聚乙二醇干扰素（PEGIFN）α治疗应答的关系。方法收集2008年1月-2012年12月在上海瑞金医院感染科就诊的212例接受PEG-IFN单药治疗48周的HBeAg阳性慢性乙型肝炎患者,采集其外周血,提取基因组DNA,并应用时间飞行质谱技术（MassARRAY）检测IPS-1基因的10个Tag-SNP位点多态性。运用卡方检验对2组等位基因频率和基因型分布情况进行分析,应用非条件性二元Logistic回归分析方法分析SNP位点、单体型与PEG-IFN疗效的关系。结果 212例患者中,应答率为34.9%（74例）,其中HBV基因C型117例,B型95例。研究发现有4个SNP位点（rs2326369、rs2464、rs6515831、rs16989000）的基因型分布在2组之间差异有统计学意义（P<0.05）。在多因素分析中,校正了性别、年龄、HBV基因型、家族史、基线HBV DNA水平及基线ALT水平后,发现3个SNP位点（rs2326369、rs6515831、rs2464）与PEG-IFN应答...
- 多态性,单核苷酸 /
- 肝炎,乙型,慢性 /
- 干扰素类
Abstract: Objective To investigate whether interferon- β promoter stimulator 1 (IPS- 1) gene polymorphisms could affect the treatment response to peginterferon alpha (PEG- IFN) in patients with HBeAg- positive chronic hepatitis B (CHB) .Methods A total of 212HBeAg- positive CHB patients treated with PEG- IFN monotherapy for 48 weeks were enrolled from the department of infectious diseases of Ruijin hospital in this study from January 2008 to December 2012.We collected peripheral blood from patients and extracted total genomic DNA.Genotype analysis was performed for 10 tag single nucleotide polymorphisms (SNPs) in IPS- 1 gene using the Sequenom MassArray system.Response was defined as cases showing hepatitis B virus (HBV) DNA level < 200 IU /ml, HBeAg seroconversion, and normal aminotransferase (ALT) levels after 48- week PEG- IFN therapy.The chi- square test was conducted to analyze the allele frequency and genotype distribution of IPS- 1 in both the response (R) and non- response (NR) groups.Binary logistic regression modeling was used to analyze the association of SNPs and haplotypes of IPS- 1 with treatment response.Results Of all the 212 patients, 95 (44.8%) were infected with HBV genotype B and 117 (55.2%) with HBV genotype C.There was a total response rate of 34.9% (74 /212) .Significant differences in genotype distributions of four SNPs (rs2326369, rs2464, rs6515831, and rs16989000) were observed between the R and NR groups (P < 0.05) .In multivariate analysis, three SNPs (rs2326369, rs6515831, and rs2464) were found to be independently associated with PEG- IFN efficacy after adjustment for sex, age, HBV genotype, family history, and baseline levels of HBV DNA and ALT: (1) rs2326369 CC genotype was independently associated with NR (OR = 0.51, 95% CI:0.28- 0.92, P = 0.026) ; (2) rs6515831 TT genotype was independently associated with R (OR = 2.08, 95% CI:1.12- 3.86, P = 0.020) ; (3) rs2464 CC genotype was independently associated with R (OR = 2.33, 95% CI:1.24- 4.37, P = 0.009) .Furthermore, two blocks were identified in this study, with block 1formed by rs16989000 and rs6515831 and block 2 formed by rs7272495, rs16989022, and rs2464.In multivariate analysis, haplotype AAC of block 2 was independently associated with R (OR = 2.05, 95% CI:1.09- 3.87, P = 0.026) .Conclusion Our study suggested that genetic variations in IPS- 1 are associated with the treatment response to PEG- IFN in HBeAg- positive CHB patients.For CHB patients treated with PEG- IFN, IPS- 1 genotyping may have a certain predictive value for curative effect.
- polymorphism, single nucleotide /
- hepatitis B, chronic /
- interferons

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