A multi-level investigation of the genetic relationship between gastroesophageal reflux disease and lung cancer.

IF 4 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2024-09-30 Epub Date: 2024-09-24 DOI:10.21037/tlcr-24-345
Dongsheng Wu, Jian Zhou, Lujia Song, Quan Zheng, Tengyong Wang, Zhizhen Ren, Yuchen Huang, Shuqiao Liu, Lunxu Liu
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引用次数: 0

Abstract

Background: Observational studies have revealed a potential association between gastroesophageal reflux disease (GERD) and lung cancer (LC), but the genetic role in their comorbidity have not been fully elucidated. This study aimed to comprehensively dissect the genetic link underlying GERD and LC.

Methods: Using large-scale genome-wide association study (GWAS) data, we investigated shared genetic architecture between GERD and LC. Our analyses encompassed genetic correlation, cross-trait meta-analysis, transcriptome-wide association studies (TWASs), and the evaluation of the causality though a bidirectional Mendelian randomization (MR) analysis with sufficient sensitivities.

Results: We identified a significant genome-wide genetic correlation between GERD and overall LC (rg =0.33, P=1.58×10-14), as well as across other subtype-specific LC (rg ranging from 0.19 to 0.39). After separating the whole genome into approximately 2,353 independent regions, 5 specific regions demonstrated significant local genetic correlation, with most significant region located at 9q33.3. Cross-trait meta-analysis revealed 22 pleiotropic loci between GERD and LC, including 3 novel loci (rs537160, rs10156445, and rs17391694). TWASs discovered a total of 49 genes shared in multiple tissues, such as lung tissues, esophagus muscularis, esophagus mucosa, and esophagus gastroesophageal junction. MR analysis suggested a significantly causal relationship between GERD and overall LC [odds ratio (OR) =1.34, 95% confidence interval (CI): 1.19-1.51], as well as other subtype-specific LC (OR ranging from 1.25 to 1.76). No evidence supports a significant causal effect of LC on GERD.

Conclusions: Our findings suggest intrinsic genetic correlation underlying GERD and LC, which provides valuable insights for screening and management of LC in individuals with GERD.

胃食管反流病与肺癌遗传关系的多层次调查。
背景:观察性研究揭示了胃食管反流病(GERD)与肺癌(LC)之间的潜在关联,但二者的遗传作用尚未完全阐明。本研究旨在全面剖析胃食管反流病和肺癌的遗传关联:方法:利用大规模全基因组关联研究(GWAS)数据,我们研究了胃食管反流病和低血糖之间的共同遗传结构。我们的分析包括遗传相关性、跨性状荟萃分析、转录组关联研究(TWAS),并通过具有足够敏感性的双向孟德尔随机化(MR)分析对因果关系进行了评估:我们发现胃食管反流病与总体低血糖之间存在显著的全基因组遗传相关性(rg =0.33,P=1.58×10-14),在其他亚型特异性低血糖之间也存在显著的相关性(rg 在 0.19 至 0.39 之间)。将全基因组分离成约 2,353 个独立区域后,有 5 个特定区域显示出显著的局部遗传相关性,其中最显著的区域位于 9q33.3。跨性状荟萃分析揭示了胃食管反流病与低血糖之间的 22 个多效应位点,其中包括 3 个新位点(rs537160、rs10156445 和 rs17391694)。TWAS在肺组织、食管肌层、食管粘膜和食管胃食管交界处等多个组织中共发现了49个共有基因。磁共振分析表明,胃食管反流病与总体低密度脂蛋白血症之间存在显著的因果关系[几率比(OR)=1.34,95% 置信区间(CI):1.19-1.51],与其他亚型特异性低密度脂蛋白血症之间也存在显著的因果关系(OR 从 1.25 到 1.76 不等)。没有证据表明低密度脂蛋白胆固醇对胃食管反流病有明显的因果关系:我们的研究结果表明,胃食管反流病与低血糖之间存在内在的遗传相关性,这为胃食管反流病患者低血糖的筛查和管理提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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