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帕金森病与胃肠道癌症风险:一项两样本孟德尔随机化研究

Parkinson's disease and the risk of gastrointestinal cancers: a two-sample Mendelian randomization study.

作者信息

Liu Zijin, Cui Lili

机构信息

Department of Gastroenterology and Hepatology, Xuanwu Hospital, Capital Medical University, Beijing, China.

Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.

出版信息

J Gastrointest Oncol. 2024 Aug 31;15(4):1475-1486. doi: 10.21037/jgo-24-106. Epub 2024 Aug 5.

Abstract

BACKGROUND

The association between Parkinson's disease (PD) and gastrointestinal (GI) cancers remains unknown. This study aims to assess the causal effect of PD on colon cancer (CC), gastric cancer (GC), esophageal cancer (EC), and rectal cancer (RC) using the two-sample Mendelian randomization (MR) method.

METHODS

Five pairs of summary datasets of genome-wide association studies (GWAS) from publicly available studies [Integrative Epidemiology Unit (IEU) OpenGWAS project, FinnGen, and GWAS Catalog database] were enrolled. The inverse variance weighted (IVW) method was used as the primary outcome for MR analysis. Cochran Q-derived, MR-Egger intercept test, MR-Pleiotropy Residual Sum and Outlier (MR-PRESSO) methods, and leave-one-out analysis were used to test heterogeneity and directional pleiotropy.

RESULTS

For the European population, no significant causal effect of PD on the risk of CC was found [odds ratio (OR) =0.9; 95%, confidence interval (CI): 1.00-1.11; P=0.42]. The same applied to the East Asian population (OR =1.05; 95% CI: 0.66-1.66; P=0.63). As for GC, no causal effect was found (OR =0.94, 95% CI: 0.89-0.99; P=0.22). Moreover, the genetic liability for PD was not associated with EC (OR =1.00; 95% CI: 0.99-1.00; P=0.32). Finally, no evidence was found for any causal effect of genetic liability for PD on an increased risk of RC (OR =1.00; 95% CI: 0.99-1.00; P=0.71).

CONCLUSIONS

There is no causal effect of genetic liability for PD on an increased risk of GI cancer.

摘要

背景

帕金森病(PD)与胃肠道(GI)癌症之间的关联尚不清楚。本研究旨在使用两样本孟德尔随机化(MR)方法评估PD对结肠癌(CC)、胃癌(GC)、食管癌(EC)和直肠癌(RC)的因果效应。

方法

纳入了来自公开研究[综合流行病学单位(IEU)OpenGWAS项目、芬兰基因研究和GWAS目录数据库]的五对全基因组关联研究(GWAS)汇总数据集。逆方差加权(IVW)方法用作MR分析的主要结果。采用Cochran Q检验、MR-Egger截距检验、MR-多效性残差和异常值(MR-PRESSO)方法以及逐一剔除分析来检验异质性和定向多效性。

结果

对于欧洲人群,未发现PD对CC风险有显著因果效应[比值比(OR)=0.9;95%,置信区间(CI):1.00-1.11;P=0.42]。东亚人群情况相同(OR =1.05;95%CI:0.66-1.66;P=0.63)。对于GC,未发现因果效应(OR =0.94,95%CI:0.89-0.99;P=0.22)。此外,PD的遗传易感性与EC无关(OR =1.00;95%CI:0.99-1.00;P=0.32)。最后,未发现有证据表明PD的遗传易感性对RC风险增加有任何因果效应(OR =1.00;95%CI:0.99-1.00;P=0.71)。

结论

PD的遗传易感性对胃肠道癌症风险增加没有因果效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb4a/11399876/15a7b5e6fd44/jgo-15-04-1475-f1.jpg

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