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HOGG1 rs1052133 多态性与前列腺癌风险:一项中国病例对照研究和荟萃分析。

hOGG1 rs1052133 Polymorphism and Prostate Cancer Risk: A Chinese Case-Control Study and Meta-Analysis.

机构信息

Department of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China (mainland).

Institute of Urology, Anhui Medical University, Hefei, Anhui, China (mainland).

出版信息

Med Sci Monit. 2022 Oct 31;28:e938012. doi: 10.12659/MSM.938012.

Abstract

BACKGROUND We performed a case-control study and an updated meta-analysis to assess the relationship between the hOGG1 rs1052133 polymorphism and prostate cancer (PCa) risk. MATERIAL AND METHODS We recruited 160 PCa cases and 243 healthy controls. For the meta-analysis, relevant studies were recruited from diverse databases up to April 2022. Genetic risk was evaluated by using an odds ratio (OR) with a corresponding 95% confidence interval (95% CI). The genotypes of this polymorphism were genotyped via the SNaPshot genotyping method. RESULTS In the case-control study, we failed to identify any association between the hOGG1 rs1052133 polymorphism and PCa risk. Negative results were also obtained when stratified analyses were performed based on the patient's prostatic-specific antigen (PSA) level and Gleason score, as well as tumor, node, and metastasis (TNM) stage. To enlarge the sample size, we performed a restricted updated meta-analysis by recruiting 10 case-control studies (including the current one), and the results suggested that genotypes of rs1052133 polymorphism were significantly associated with an elevated risk of PCa in 2 genetic models - the heterozygote and dominant models. In the stratification analysis by population ethnicity, a significant association of this polymorphism with susceptibility to PCa was found both in the Asian populations and White populations. CONCLUSIONS Our case-control and updated meta-analysis study suggest that the hOGG1 rs1052133 polymorphism is a susceptibility factor for PCa, but still needs to be further verified in the Chinese population.

摘要

背景

我们进行了病例对照研究和更新的荟萃分析,以评估 hOGG1 rs1052133 多态性与前列腺癌(PCa)风险之间的关系。

材料与方法

我们招募了 160 例 PCa 病例和 243 例健康对照。为了进行荟萃分析,我们从不同的数据库中招募了截至 2022 年 4 月的相关研究。使用比值比(OR)及其相应的 95%置信区间(95%CI)来评估遗传风险。该多态性的基因型通过 SNaPshot 基因分型方法进行基因分型。

结果

在病例对照研究中,我们未能发现 hOGG1 rs1052133 多态性与 PCa 风险之间存在任何关联。当根据患者的前列腺特异性抗原(PSA)水平和 Gleason 评分以及肿瘤、淋巴结和转移(TNM)分期进行分层分析时,也得到了阴性结果。为了扩大样本量,我们通过招募 10 项病例对照研究(包括本次研究)进行了受限更新的荟萃分析,结果表明,rs1052133 多态性的基因型与 2 种遗传模型(杂合子和显性模型)下 PCa 的风险升高显著相关。在按人群种族进行的分层分析中,发现该多态性与 PCa 的易感性在亚洲人群和白人人群中均存在显著关联。

结论

我们的病例对照和更新的荟萃分析研究表明,hOGG1 rs1052133 多态性是 PCa 的易感因素,但仍需要在中国人群中进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f797/9635216/10bd2429ffd4/medscimonit-28-e938012-g001.jpg

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