与炎症性肠病、缺血性心脏病、心房颤动和扑动相关的共享基因位点的鉴定

IF 2.3 3区 医学 Q2 GENETICS & HEREDITY
Guojian Chen, Qinghua Luo, Chengcheng Wu, Mingjun Xie
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引用次数: 0

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)有一定的关联,值得在遗传结构水平上进一步探索。本研究针对IHD、心房颤动和扑动、IBD的全基因组关联研究(GWAS)数据,从遗传相关性和共享位点鉴定两个维度进行分析。首先,利用连锁不平衡评分回归和遗传协方差分析来评估总体遗传相关性。随后,利用局部祖先变异关联(local Ancestry Variance association, LAVA)分析确定了局部基因组区域的关联模式。采用孟德尔随机化(MR)评估因果效应。基于条件/联合错误发现率(cond/conjFDR)统计框架,分析了不同性状间的遗传重叠。最后,通过结合共轭fdr分析和GWAS多性状分析(MTAG),确定了这些性状之间的共享位点。在基因组水平上,在IHD、心房颤动和扑动、IBD和克罗恩病(CD)之间观察到显著的总体相关性,而与溃疡性结肠炎的相关性似乎不太明显。在地方层面,IHD和IBD(包括亚型)在多个地区显示出显著的相关性。然而,心房颤动和扑动仅在CD背景下表现出局部关联。通过共轭fdr分析,证实了这些疾病之间的遗传重叠。此外,通过整合共轭fdr和MTAG分析,确定了几个共享的遗传位点,这些基因在IHD和IBD(包括亚型)中都得到了证实,如SMAD3、PLCG2、ZNF831、PTPN22、RP11-136O12.2和RP11-449I17.5。此外,在心房颤动和扑动与IBD(包括亚型)之间的分析中发现了6个共同基因,如ZMIZ1、MTHFS、ERAP2、GNA12和RP1-15D23.2。本研究为IHD、心房颤动和扑动以及IBD合并症之间的遗传关联提供了经验证据,为IBD合并IHD或心房颤动和扑动的病例提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Shared Genetic Loci Associated With Inflammatory Bowel Disease, Ischemic Heart Disease, and Atrial Fibrillation and Flutter

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.

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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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