Suppr超能文献

TP53基因密码子72多态性与急性髓系白血病易感性的关联:基于荟萃分析的证据

Association Between TP53 Gene Codon 72 Polymorphism and Acute Myeloid Leukemia Susceptibility: Evidence Based on a Meta-Analysis.

作者信息

Ruan Xiao-Lan, Li Sheng, Geng Peiliang, Zeng Xian-Tao, Yu Guo-Zheng, Meng Xiang-Yu, Gao Qing-Ping, Ao Xu-Bin

机构信息

Department of Hematology, Targeted Biotherapy Key Laboratory of Ministry of Education, Renmin Hospital of Wuhan University, Wuhan, Hubei, China (mainland).

Center for Evidence-Based and Translational Medicine, Zhongnan Hospital, Wuhan University, Wuhan, Hubei, China (mainland).

出版信息

Med Sci Monit. 2015 Oct 9;21:3048-53. doi: 10.12659/MSM.894625.

Abstract

BACKGROUND

Many studies have reported that the p53 codon 72 polymorphism is associated with acute myeloid leukemia (AML) susceptibility; however, the conclusions are inconsistent. Therefore, we performed this meta-analysis to obtain a more precise result.

MATERIAL AND METHODS

We searched PubMed to identify relevant studies, and 6 published case-control studies were retrieved, including 924 AML patients and 3832 controls. Odds ratio (OR) with corresponding 95% confidence interval (95%CI) was applied to assess the association between p53 codon 72 polymorphism and AML susceptibility. The meta-analysis was performed with Comprehensive Meta-Analysis software, version 2.2.

RESULTS

Overall, no significant association between p53 codon 72 polymorphism and AML susceptibility was found in this meta-analysis (Pro vs. Arg: OR=0.94, 95%CI=0.81-1.10; Pro/Pro vs. Arg/Arg: OR=0.93, 95%CI=0.71-1.22; Arg/Pro vs. Arg/Arg: OR=0.79, 95%CI=0.55-1.13; (Pro/Pro + Arg/Pro) vs. Arg/Arg: OR=0.84, 95%CI=0.62-1.13; Pro/Pro vs. (Arg/Arg + Arg/Pro): OR=1.06, 95%CI=0.83-1.35). Similar results were also found in stratified analysis according to ethnicity and source of controls.

CONCLUSIONS

Our meta-analysis demonstrates that p53 codon 72 polymorphism may not be a risk factor for AML, which should be verified in future studies.

摘要

背景

许多研究报告称,p53基因第72位密码子多态性与急性髓系白血病(AML)易感性相关;然而,结论并不一致。因此,我们进行了这项荟萃分析以获得更精确的结果。

材料与方法

我们检索了PubMed以确定相关研究,共检索到6项已发表的病例对照研究,包括924例AML患者和3832例对照。采用比值比(OR)及相应的95%置信区间(95%CI)来评估p53基因第72位密码子多态性与AML易感性之间的关联。使用Comprehensive Meta-Analysis软件2.2版进行荟萃分析。

结果

总体而言,在这项荟萃分析中未发现p53基因第72位密码子多态性与AML易感性之间存在显著关联(脯氨酸(Pro)与精氨酸(Arg):OR = 0.94,95%CI = 0.81 - 1.10;Pro/Pro与Arg/Arg:OR = 0.93,95%CI = 0.71 - 1.22;Arg/Pro与Arg/Arg:OR = 0.79,95%CI = 0.55 - 1.13;(Pro/Pro + Arg/Pro)与Arg/Arg:OR = 0.84,95%CI = 0.62 - 1.13;Pro/Pro与(Arg/Arg + Arg/Pro):OR = 1.06,95%CI = 0.83 - 1.35)。根据种族和对照来源进行的分层分析也得到了类似结果。

结论

我们的荟萃分析表明,p53基因第72位密码子多态性可能不是AML的危险因素,这一点有待未来研究加以验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2165/4603608/8db49d091257/medscimonit-21-3048-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验