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ADH1B Arg47His 多态性与高发亚洲人群食管癌风险相关:来自荟萃分析的证据。

ADH1B Arg47His polymorphism is associated with esophageal cancer risk in high-incidence Asian population: evidence from a meta-analysis.

机构信息

Department of Pathology, Shantou University Medical College, Shantou, China.

出版信息

PLoS One. 2010 Oct 27;5(10):e13679. doi: 10.1371/journal.pone.0013679.

Abstract

BACKGROUND AND OBJECTIVES

Incidence of Esophageal squamous cell carcinoma (ESCC) is prevalent in Asian populations, especially in the ones from the "Asian esophageal cancer belt" along the Silk Road and the ones from East Asia (including Japan). Silk Road and Eastern Asia population genetics are relevant to the ancient population migration from central China. The Arg47His (rs1229984) polymorphism of ADH1B is the highest in East Asians, and ancient migrations along the Silk Road were thought to be contributive to a frequent ADH1B*47His allele in Central Asians. This polymorphism was identified as responsible for susceptibility in the first large-scale genome-wide association study of ESCC and that's explained by its modulation of alcohol oxidization capability. To investigate the association of ADH1B Arg47His with ESCC in Asian populations under a common ancestry scenario of the susceptibility loci, we combined all available studies into a meta-analysis.

METHODS

A dataset composed of 4,220 cases and 8,946 controls from twelve studies of Asian populations was analyzed for ADH1B Arg47His association with ESCC and its interactions with alcohol drinking and ALDH2 Glu504Lys. Heterogeneity among studies and their publication bias were also tested.

RESULTS

The ADH1B*47Arg allele was found to be associated to increased risk of ESCC, with the odds ratios (OR) being 1.62 (95% CI: 1.49-1.76) and 3.86 (2.96-5.03) for the His/Arg and the Arg/Arg genotypes, respectively. When compared with the His/His genotype of non-drinkers, the Arg/Arg genotype can interact with alcohol drinking and greatly increase the risk of ESCC (OR = 20.69, 95%CI: 5.09-84.13). Statistical tests also showed gene-gene interaction of ADH1B Arg+ with ALDH2 Lys+ can bring more risk to ESCC (OR  = 13.46, 95% CI: 2.32-78.07).

CONCLUSION

Revealed by this meta-analysis, ADH1B47Arg as a common ancestral allele can significantly increase the risk of ESCC in Asians, especially when coupled with alcohol drinking or the ALDH2504Lys allele.

摘要

背景与目的

食管鳞状细胞癌(ESCC)的发病率在亚洲人群中较为普遍,尤其是丝绸之路沿线和东亚地区(包括日本)的人群。丝绸之路和东亚地区的人口遗传学与从中原地区发生的古代人口迁移有关。ADH1B 基因的 Arg47His(rs1229984)多态性在东亚人群中最高,而古代沿丝绸之路的迁移被认为是中亚人群中频繁出现 ADH1B*47His 等位基因的原因。该多态性被确定为导致 ESCC 的第一个大规模全基因组关联研究的易感性的原因,这可以通过其对酒精氧化能力的调节来解释。为了在易感性基因座的共同祖先背景下研究 ADH1B Arg47His 与 ESCC 在亚洲人群中的关联,我们将所有可用的研究合并为一项荟萃分析。

方法

对来自亚洲人群的 12 项研究中的 4220 例病例和 8946 例对照组成的数据集进行分析,以研究 ADH1B Arg47His 与 ESCC 的关联及其与饮酒和 ALDH2 Glu504Lys 的相互作用。还测试了研究之间的异质性及其发表偏倚。

结果

ADH1B*47Arg 等位基因与 ESCC 风险增加相关,His/Arg 和 Arg/Arg 基因型的优势比(OR)分别为 1.62(95%CI:1.49-1.76)和 3.86(2.96-5.03)。与非饮酒者的 His/His 基因型相比,Arg/Arg 基因型可与饮酒相互作用,大大增加 ESCC 的风险(OR=20.69,95%CI:5.09-84.13)。统计检验还表明,ADH1B Arg+与 ALDH2 Lys+的基因-基因相互作用可使 ESCC 的风险增加更多(OR=13.46,95%CI:2.32-78.07)。

结论

本荟萃分析表明,ADH1B47Arg 作为一个共同的祖先等位基因,可显著增加亚洲人患 ESCC 的风险,尤其是当与饮酒或 ALDH2504Lys 等位基因相结合时。

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