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从自身免疫性疾病的角度探索炎症性肠病的遗传成分和多组学来源。

Exploring the genetic components and multi-omics sources of inflammatory bowel disease from the perspective of autoimmune disorders.

作者信息

Wang Zhonghai, Chen Xin, Zhang Quan-Bo, Wang Han

机构信息

Department of Geriatrics, North Sichuan Medical College, Nanchong, Sichuan, China.

Department of Cardiology, The Third People'S Hospital of Chengdu, Chengdu, Sichuan, China.

出版信息

Clin Rheumatol. 2025 Apr 10. doi: 10.1007/s10067-025-07422-y.

Abstract

BACKGROUND

Inflammatory bowel disease (IBD) and autoimmune disorders result from immune system dysregulation. However, the genetic overlap between them remains unclear. Our study aimed to investigate the genetic mechanisms and structure of IBD from the perspective of autoimmune disorders.

METHODS

The genetic correlation (rg) between traits can provide valuable information about the shared underlying biological mechanisms. Utilizing summary statistics from genome-wide association studies, we delved into the genetic correlation, shared inheritance, and potential causality of IBD (N = 34,652) with autoimmune disorders (N = 1,755,610). We performed transcriptomics at the gene level, multi-marker analyses of genome annotations, and enrichment analyses of biological pathways to highlight shared and diverse perspectives.

RESULTS

There were significant genetic correlations between IBD and ankylosing spondylitis (rg = 0.327), rheumatoid arthritis (rg = 0.242), type 1 diabetes (rg = - 0.061), psoriasis (rg = 0.246), and ankylosing spondylitis (rg = 0.308). We identified 110 unique regions (including 5p33.3, 10q25.3, and 22q13.31) after a consistent study at the gene levels. By implementing transcriptomics techniques, we discovered potential common biological mechanisms in several tissues, including blood, spleen, thyroid, and pancreas, revealing potential common biological mechanisms involving lincRNA, protein-coding, and pseudogenes.

CONCLUSION

Our study demonstrated hypothesized pleiotropic genomic regions that provide important clues to delve into the genetic basis of IBD and autoimmune disorders on the basis of multi-omics. Moreover, we have identified shared pathogenic processes and potential common therapeutic targets among these diseases. Key Points • The finding provides a new perspective on the genetic basis of inflammatory bowel disease and autoimmune disease across multi-omics platforms. • Fine mapping of functional summary-based imputation and causal genomes has identified hypothesized pleiotropic genomic regions. • The identified genes and pathways may offer innovative targets for the prevention of immune-related diseases.

摘要

背景

炎症性肠病(IBD)和自身免疫性疾病是由免疫系统失调引起的。然而,它们之间的遗传重叠尚不清楚。我们的研究旨在从自身免疫性疾病的角度研究IBD的遗传机制和结构。

方法

性状之间的遗传相关性(rg)可以提供有关共同潜在生物学机制的有价值信息。利用全基因组关联研究的汇总统计数据,我们深入研究了IBD(N = 34,652)与自身免疫性疾病(N = 1,755,610)之间的遗传相关性、共同遗传和潜在因果关系。我们在基因水平上进行了转录组学分析、基因组注释的多标记分析以及生物途径的富集分析,以突出共同和不同的观点。

结果

IBD与强直性脊柱炎(rg = 0.327)、类风湿性关节炎(rg = 0.242)、1型糖尿病(rg = -0.061)、银屑病(rg = 0.246)和强直性脊柱炎(rg = 0.308)之间存在显著的遗传相关性。在基因水平进行一致性研究后,我们确定了110个独特区域(包括5p33.3、10q25.3和22q13.31)。通过实施转录组学技术,我们在包括血液、脾脏、甲状腺和胰腺在内的多个组织中发现了潜在的共同生物学机制,揭示了涉及长链非编码RNA、蛋白质编码和假基因的潜在共同生物学机制。

结论

我们的研究证明了假设的多效性基因组区域,这些区域为在多组学基础上深入研究IBD和自身免疫性疾病的遗传基础提供了重要线索。此外,我们已经确定了这些疾病之间共同的致病过程和潜在的共同治疗靶点。要点• 这一发现为跨多组学平台的炎症性肠病和自身免疫性疾病的遗传基础提供了新的视角。• 基于功能汇总的归因和因果基因组的精细定位确定了假设的多效性基因组区域。• 确定的基因和途径可能为免疫相关疾病的预防提供创新靶点。

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