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与炎症性肠病、缺血性心脏病以及心房颤动和心房扑动相关的共享基因位点的鉴定。

Identification of Shared Genetic Loci Associated With Inflammatory Bowel Disease, Ischemic Heart Disease, and Atrial Fibrillation and Flutter.

作者信息

Chen Guojian, Luo Qinghua, Wu Chengcheng, Xie Mingjun

机构信息

Department of Gastrointestinal Surgery, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.

Clinical Medical College, Jiangxi University of Chinese Medicine, Nanchang, China.

出版信息

Clin Genet. 2025 Sep;108(3):302-312. doi: 10.1111/cge.14749. Epub 2025 May 8.

Abstract

The occurrence of ischemic heart disease (IHD), atrial fibrillation, and flutter demonstrates certain associations with inflammatory bowel disease (IBD), warranting further exploration at the genetic architecture level. This study focused on genome-wide association study (GWAS) data of IHD, atrial fibrillation and flutter, and IBD, analyzing from two dimensions: genetic correlation and shared locus identification. Initially, linkage disequilibrium score regression and genetic covariance analyzer were utilized to assess the overall genetic correlations. Subsequently, the association patterns of local genomic regions were determined using Local Ancestry Variance Association (LAVA) analysis. Mendelian randomization (MR) was employed to assess causal effects. The genetic overlap among different traits was analyzed based on the statistical framework of conditional/conjunctional false discovery rate (cond/conjFDR). Finally, shared loci across these traits were identified by integrating conjFDR analysis with GWAS multi-trait analysis (MTAG). At the genomic level, significant overall correlations were observed among IHD, atrial fibrillation and flutter, and IBD and Crohn's disease (CD), while associations with ulcerative colitis appeared less pronounced. At the local level, IHD and IBD (including subtypes) showed significant associations in multiple regions. However, atrial fibrillation and flutter exhibited local associations only in the context of CD. Through conjFDR analysis, the genetic overlap across these diseases was validated. Additionally, several shared genetic loci were identified by integrating conjFDR and MTAG analyses, with genes confirmed in both IHD and IBD (including subtypes), such as SMAD3, PLCG2, ZNF831, PTPN22, RP11-136O12.2, and RP11-449I17.5. Moreover, six common genes were identified in the analysis between atrial fibrillation and flutter and IBD (including subtypes), such as ZMIZ1, MTHFS, ERAP2, GNA12, and RP1-15D23.2. This study offers empirical evidence of the genetic association between IHD, atrial fibrillation and flutter, and IBD comorbidity, providing new insights for cases where IBD co-occurs with IHD or atrial fibrillation and flutter.

摘要

缺血性心脏病(IHD)、心房颤动和扑动的发生与炎症性肠病(IBD)存在一定关联,这值得在基因结构层面进行进一步探索。本研究聚焦于IHD、心房颤动和扑动以及IBD的全基因组关联研究(GWAS)数据,从两个维度进行分析:遗传相关性和共享基因座识别。首先,利用连锁不平衡评分回归和遗传协方差分析器来评估总体遗传相关性。随后,使用局部祖先方差关联(LAVA)分析来确定局部基因组区域的关联模式。采用孟德尔随机化(MR)来评估因果效应。基于条件/联合错误发现率(cond/conjFDR)的统计框架分析不同性状之间的遗传重叠。最后,通过将conjFDR分析与GWAS多性状分析(MTAG)相结合,识别这些性状之间的共享基因座。在基因组水平上,观察到IHD、心房颤动和扑动以及IBD与克罗恩病(CD)之间存在显著的总体相关性,而与溃疡性结肠炎的关联似乎不太明显。在局部水平上,IHD与IBD(包括各亚型)在多个区域表现出显著关联。然而,心房颤动和扑动仅在CD背景下表现出局部关联。通过conjFDR分析,验证了这些疾病之间的遗传重叠。此外,通过整合conjFDR和MTAG分析,识别出了几个共享遗传基因座,在IHD和IBD(包括各亚型)中均得到确认的基因,如SMAD3、PLCG2、ZNF831、PTPN22、RP11 - 136O12.2和RP11 - 449I17.5。此外,在心房颤动和扑动与IBD(包括各亚型)的分析中识别出六个共同基因,如ZMIZ1、MTHFS、ERAP2、GNA12和RP1 - 15D23.2。本研究为IHD、心房颤动和扑动与IBD合并症之间的遗传关联提供了实证依据,为IBD与IHD或心房颤动和扑动同时发生的情况提供了新的见解。

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