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LEPR G1n223Arg多态性对不同种族人群中乳腺癌危险性影响的meta分析
引用本文:许晔琼,李瑞,高天翼,顾玲,聂珍琳,陈丽萍,宋国齐,王书奎.LEPR G1n223Arg多态性对不同种族人群中乳腺癌危险性影响的meta分析[J].医疗设备信息,2012(11):26-30,13.
作者姓名:许晔琼  李瑞  高天翼  顾玲  聂珍琳  陈丽萍  宋国齐  王书奎
作者单位:南京医科大学附属南京第一医院中心实验室,江苏南京210006
基金项目:国家自然科学基金(81172141).
摘    要:瘦素和瘦素受体参与了乳腺癌的发生发展过程。在瘦素受体基因(LEPR)6号外显子上第223个密码子A到G的转变可以导致谷氨酸到精氨酸的替换(Gln223Arg)。许多已发表的病例对照研究评价了LEPRGln223Arg多态性与乳腺癌的关系。然而,却未得出一致的结论。本篇meta分析囊括了8篇文献来评价LEPRGln223Arg多态性与乳腺癌的联系。用总体合并OR值作为研究共显性模型、隐性模型、显性模型的指标。结果显示总体研究中隐性模型(OR=1.32,95%CI:1.03~1.69)和Arg/Gln vs Gin/Gin基因型(OR=1.16,95%CI:1.01~1.34)显著提高了乳腺癌的危险性。种族分层分析中发现,非洲人群的以下几个基因型会提高患乳腺癌的危险性:Arg/Arg vs 8Gln/Gln(OR=1.86,95%CI:1.28-2.71),Arg/Gln vs GIn/Gln(OR=1.48,95%CI:1.10—1.99),显性模型(OR=1.60,95%CI:1.21~2.11)和隐性模型(OR=1.48,95%cI:1.07~2.05);亚洲人群中,Arg/ArgvsGin/Gin基因型(OR=6.79,95%CI:3.42~13.47)和显性模型(OR=2.03,95%CI:1.42~2.90)提高了患乳腺癌的危险性。在欧洲人群中任何基因模型都没有发现能显著提高乳腺癌的危险性。总而言之,LEPR223Arg是乳腺癌发展的低风险因素,特别是在非洲女性中。

关 键 词:LEPR  乳腺癌  meta分析  分子流行病学

meta Analysis of Effect ofLEPR G1n223Arg Polymorphism on Breast Cancer Risk in Different Ethnic Populations
XU Ye-qiong,LI Rui,GAO Tian-yi,GU Ling,NIE Zhen-lin,CHEN Li-ping,SONG Guo-qi,WANG Shu-kui.meta Analysis of Effect ofLEPR G1n223Arg Polymorphism on Breast Cancer Risk in Different Ethnic Populations[J].Information of Medical Equipment,2012(11):26-30,13.
Authors:XU Ye-qiong  LI Rui  GAO Tian-yi  GU Ling  NIE Zhen-lin  CHEN Li-ping  SONG Guo-qi  WANG Shu-kui
Institution:(Central Laboratory, Nanjing First Hospital, Nanj-ng Medical University, Nanjing Jiangsu 210006, China)
Abstract:Leptin and leptin receptor have been implicated in processes of breast cancer. An A to G transition of codon 223^th in exon 6 of leptin receptor gene (LEPR) can result in the substitution from glutamine to arginine (Gln223Arg). A variety of case--control papers have been published to evaluate the association between LEPR Gln223Arg polymorphism and breast cancer. However, they have got contradictory conclusions. This meta analysis enrolls 8 papers to evaluate the connection of them. The pooled ORs are took for codominant model, recessive model, dominant model. The result shows that recessive model (OR=1.32, 95%CI: 1.03-1.69) and genotype Arg/Gln vs Gln/Gln (OR=1.16, 95%CI: 1.01-1.34) significantly improve breast cancer risk in overall study. In racial stratified analysis, some genotypes among Africans would significantly increase the risk: Arg/Arg vs Gln/Gln(OR=I.86, 95%CI: 1.28-2.71), Arg/GIn vs Gln/GIn(OR=l.48, 95%CI: 1.10-1.99), dominant model(OR=l.60, 95%CI: 1.21-2.11) and recessive model(OR=1.48, 95%CI: 1.07-2.05); for Asians, Arg/Arg vs GIn/GIn(OR=6.79, 95%C1: 3.42-13.47) and dominant model(OR=2.03, 95%CI: 1.42-2.90). However, no genetic models are found among Europeans which significantly increase cancer risk. In conclusion, the L1EPR 223Arg is a low risk factor for developing breast cancer, especially for African women.
Keywords:leptin receptor gene  breast cancer  meta analysis  molecular epidemiotogy
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