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KIF1B 是与 HBV 相关的肝细胞癌易感性基因,但与慢性乙型肝炎的发展无关。

HBV-related hepatocellular carcinoma susceptibility gene KIF1B is not associated with development of chronic hepatitis B.

机构信息

Education Key Laboratory of Environment and Health, Department of Epidemiology and Biostatistics and Ministry, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

出版信息

PLoS One. 2012;7(2):e28839. doi: 10.1371/journal.pone.0028839. Epub 2012 Feb 21.

Abstract

BACKGROUND

A recent genome-wide association study has identified a new susceptibility locus, kinesin family member 1B gene (KIF1B), strongly associated with progression from chronic hepatitis B (CHB) to hepatitis B virus-related hepatocellular carcinoma (HCC) in Chinese population, this study was carried out to explore the role of the genetic variants in KIF1B in the development of chronic hepatitis B.

METHODOLOGY/PRINCIPAL FINDINGS: Three KIF1B polymorphisms (rs8019, rs17401924, and rs17401966) were selected and genotyped in 473 CHB patients and 580 controls with no history of CHB. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by logistic regression model. None of these three SNPs showed association with CHBs after adjusting for age and gender. Equivalence-based method analysis confirmed the absence of association. In the further haplotype analysis, three common haplotypes were observed in this study population, but no significant effect was also found for haplotypes in the progression to CHB.

CONCLUSIONS/SIGNIFICANCE: This study showed the new locus identified for HCC, KIF1B, was not associated with progression to CHB, implying distinct genetic susceptibility factor contributes to the progression from hepatitis B virus infection to HCC. Nevertheless, further comprehensive analyses are warranted to dissect the mechanism.

摘要

背景

最近的全基因组关联研究发现了一个新的易感基因座,驱动蛋白家族成员 1B 基因(KIF1B),与中国人群从慢性乙型肝炎(CHB)向乙型肝炎病毒相关肝细胞癌(HCC)的进展密切相关,本研究旨在探讨 KIF1B 基因遗传变异在慢性乙型肝炎发病机制中的作用。

方法/主要发现:选择三个 KIF1B 多态性(rs8019、rs17401924 和 rs17401966),在 473 例 CHB 患者和 580 例无 CHB 病史的对照中进行基因分型。采用 logistic 回归模型计算比值比(OR)和 95%置信区间(CI)。在调整年龄和性别后,这三个 SNP 均与 CHB 无关。等效性检验分析也证实了这一点。在进一步的单体型分析中,在本研究人群中观察到三个常见单体型,但单体型与 CHB 进展也没有显著相关性。

结论/意义:本研究表明,新发现的 HCC 易感基因座 KIF1B 与 CHB 进展无关,这表明不同的遗传易感因素可能导致乙型肝炎病毒感染向 HCC 的进展。然而,需要进一步的综合分析来阐明其机制。

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