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XPD Asp312Asn基因多态性与食管癌易感性的关联:一项荟萃分析。

Association between XPD Asp312Asn polymorphism and esophageal cancer susceptibility: a meta-analysis.

作者信息

Duan Xiao-Li, Gong Heng, Zeng Xian-Tao, Ni Xiao-Bing, Yan Yan, Chen Wen, Liu Guo-Lei

机构信息

Department of Digestion Medcine, Taihe Hospital, Hubei University of Medcine, Shiyan, Hubei Province, China.

出版信息

Asian Pac J Cancer Prev. 2012;13(7):3299-303. doi: 10.7314/apjcp.2012.13.7.3299.

DOI:10.7314/apjcp.2012.13.7.3299
PMID:22994751
Abstract

OBJECTIVE

To investigate the association between xeroderma pigmentosum group D (XPD) Asp312Asn polymorphism and esophageal cancer (EC) susceptibility by meta-analysis.

METHODS

We searched PubMed up to April 9th, 2012, to identify relevant papers, and 8 published case-control studies including 2165 EC patients and 3141 healthy controls were yielded. Odds ratios (ORs) with relevant 95% confidence intervals (CIs) were applied to assess the association between XPD Asp312Asn polymorphism and EC susceptibility with the Comprehensive Meta-Analysis software, version 2.2.

RESULTS

Overall, the meta-analysis results suggested the XPD Asp312Asn polymorphism to be significantly associated with EC susceptibility [(Asn/Asn+Asp/Asn) vs. Asp/Asp: OR=1.20, 95%CI=1.05-1.36, p=0.01; and Asp/Asn vs. Asp/Asp: OR=1.15, 95%CI=1.01-1.31, p=0.04]. In the subgroup analysis by ethnicity and cancer type, significantly associations were found for Caucasian populations [(Asn/Asn+Asp/Asn) vs. Asp/Asp: OR=1.26, 95%CI=1.08-1.47, p<0.001; Asp/Asn vs. Asp/Asp: OR=1.19, 95%CI=1.02- 1.40, p=0.03] and esophageal squamous cell carcinoma [(Asn/Asn+Asp/Asn) vs. Asp/Asp: OR=1.19, 95%CI=1.01-1.41, p=0.04]. There was no heterogeneity and no publication bias existed.

CONCLUSIONS

This meta-analysis shows that the XPD Asp312Asn polymorphism may be a risk factor for developing EC, especially for Caucasian populations and esophageal squamous cell carcinoma.

摘要

目的

通过荟萃分析研究着色性干皮病D组(XPD)Asp312Asn多态性与食管癌(EC)易感性之间的关联。

方法

检索截至2012年4月9日的PubMed以确定相关论文,共获得8项已发表的病例对照研究,包括2165例EC患者和3141例健康对照。使用综合荟萃分析软件2.2版应用比值比(OR)及相关的95%置信区间(CI)来评估XPD Asp312Asn多态性与EC易感性之间的关联。

结果

总体而言,荟萃分析结果表明XPD Asp312Asn多态性与EC易感性显著相关[(Asn/Asn + Asp/Asn)与Asp/Asp相比:OR = 1.20,95%CI = 1.05 - 1.36,p = 0.01;Asp/Asn与Asp/Asp相比:OR = 1.15,95%CI = 1.01 - 1.31,p = 0.04]。在按种族和癌症类型进行的亚组分析中,发现白种人群[(Asn/Asn + Asp/Asn)与Asp/Asp相比:OR = 1.26,95%CI = 1.08 - 1.47,p < 0.001;Asp/Asn与Asp/Asp相比:OR = 1.19,95%CI = 1.02 - 1.40,p = 0.03]和食管鳞状细胞癌[(Asn/Asn + Asp/Asn)与Asp/Asp相比:OR = 1.19,95%CI = 1.01 - 1.41,p = 0.04]存在显著关联。不存在异质性和发表偏倚。

结论

这项荟萃分析表明,XPD Asp312Asn多态性可能是发生EC的一个危险因素,尤其是对白种人群和食管鳞状细胞癌而言。

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