胃肠道疾病和肾结石疾病之间的遗传联系:来自全基因组交叉性状分析的见解。

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Kidney360 Pub Date : 2025-01-03 DOI:10.34067/KID.0000000689
Yicun Wang, Zhiyi Zhao, Runyi Wang, Xiaopeng Hu
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引用次数: 0

摘要

背景:肾结石疾病(KSD)与胃肠道疾病之间的流行病学关联已被报道,肠道内稳态在结石形成中起关键作用。然而,潜在的内在联系并没有得到充分的理解。本研究旨在探讨这两种疾病之间的遗传关联。方法:我们获得了KSD与胃肠道疾病的大规模全基因组关联研究的汇总统计数据,包括胃食管反流病(GERD)、消化性溃疡病、炎症性肠病及其亚型、肠易激综合征(IBS)和憩室病(N = 311,254 ~ 720,199)。首先估计了它们的总体遗传相关性。然后,我们通过交叉性状分析检测了共享的遗传结构,包括多效单核苷酸多态性(snp)、位点、基因和生物过程。此外,进行双向孟德尔随机化(MR)分析以寻找其因果关系。结果:KSD与5种胃肠道疾病均有显著正相关。交叉性状分析鉴定出3184个潜在的多效性snp,其中33个是两种疾病共有的多效性位点。基因水平分析揭示了8个多效性致病基因,主要富集于离子稳态和维生素d反应的生物学途径中。在MR分析中,我们发现了从胃食管反流、肠易激综合征和克罗恩病到KSD的因果关系,但没有观察到反向因果关系。结论:我们的研究证明了KSD与胃肠道疾病之间的正遗传联系,并报道了多效变异、位点和基因,暗示了结石疾病发病机制的潜在生物学机制。这些发现进一步支持了肠肾轴的作用,并为这些疾病的预防、协同调节和治疗提供了遗传基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Links Between Gastrointestinal Disorders and Kidney Stone Disease: Insights from Genome-Wide Cross-Trait Analysis.

Background: Epidemiological associations between kidney stone disease (KSD) and gastrointestinal disorders have been reported, and intestinal homeostasis plays a critical role in stone formation. However, the underlying intrinsic link is not adequately understood. This study aims to investigate the genetic associations between these two types of diseases.

Methods: We obtained summary statistics from large-scale genome-wide association studies of KSD and gastrointestinal diseases, including gastroesophageal reflux disease (GERD), peptic ulcer disease, inflammatory bowel disease and its subtypes, irritable bowel syndrome (IBS) and diverticular disease (N = 311,254 to 720,199). Their overall genetic correlations were first estimated. We then detected the shared genetic architecture, including pleiotropic single nucleotide polymorphisms (SNPs), loci, genes and biological processes, through cross-trait analyses. In addition, bidirectional Mendelian randomization (MR) analysis was performed to look for their causal relationships.

Results: We found significantly positive genetic correlations between KSD and all five gastrointestinal diseases. The cross-trait analysis identified 3184 potential pleiotropic SNPs, and 33 of which were pleiotropic loci shared by the two disorders. Gene-level analyses revealed 8 pleiotropic causal genes, primarily enriched in biological pathways involving ion homeostasis and response to vitamin D. In the MR analysis, we detected causal effects from GERD, IBS and Crohn's disease to KSD, while no reverse causality was observed.

Conclusions: Our study demonstrated the positive genetic links between KSD and gastrointestinal diseases and reported pleiotropic variants, loci, and genes, implicating potential biological mechanisms in the pathogenesis of stone disease. These findings further support the role of the gut-kidney axis and provide a genetic basis for the prevention, coregulation and treatment of these diseases.

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Kidney360
Kidney360 UROLOGY & NEPHROLOGY-
CiteScore
3.90
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