Novel Susceptibility Genes for Sepsis Revealed by a Cross-Tissue Transcriptome-Wide Association Study.

IF 2.9 3区 医学 Q2 CRITICAL CARE MEDICINE
SHOCK Pub Date : 2025-07-23 DOI:10.1097/SHK.0000000000002652
Linfeng Tao, Ning Zhu, Yue Zhu, Chao Li, Yiyuan Pan, Yan Chen, Jun Liu
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引用次数: 0

Abstract

Background: Sepsis, a life-threatening syndrome triggered by a dysregulated host response to infection, continues to impose a substantial global health burden. Advances in genomics and transcriptomics now enable systematic exploration of sepsis pathogenesis at the genetic level. The integration of genome-wide association studies (GWAS) and transcriptome-wide association studies (TWAS) offers a powerful framework to identify causal genetic variants and delineate molecular mechanisms underlying sepsis susceptibility and clinical outcomes.

Methods: A cross-tissue TWAS was implemented using UTMOST to integrate sepsis GWAS summary statistics with transcriptomic data from the Genotype-Tissue Expression version 8 (GTEx v8) project. Candidate genes were validated through complementary approaches: FUSION, FOCUS, and MAGMA. Tissue-specific and pathway enrichment analyses were applied to prioritize sepsis-associated genes and characterize their functional roles in disease-relevant biological processes. Bayesian colocalization and two-sample Mendelian randomization (MR) analyses were employed to infer putative causal relationships between prioritized genes and sepsis risk.

Results: Four genes-ZCCHC4, PDGFB, C18orf54, and ATG4B-demonstrated significant associations with sepsis susceptibility in cross-tissue analyses. Two-sample MR provided evidence for causal effects of genetically regulated expression of these genes on sepsis risk. Bayesian colocalization identified shared causal variants between sepsis-associated loci and expression quantitative trait loci (eQTLs), implicating dysregulation of inflammatory and autophagy pathways in sepsis pathogenesis.

Conclusion: Our results highlight the efficacy of cross-tissue TWAS in mapping sepsis-associated loci and elucidating the genetic architecture underlying sepsis susceptibility. These prioritized loci constitute compelling targets for functional validation and represent actionable candidates for therapeutic intervention in sepsis.

跨组织转录组关联研究揭示了脓毒症的新易感基因。
背景:败血症是一种由宿主对感染反应失调引发的危及生命的综合征,继续给全球健康造成重大负担。基因组学和转录组学的进步使得在遗传水平上对败血症发病机制进行系统的探索成为可能。全基因组关联研究(GWAS)和转录组关联研究(TWAS)的整合提供了一个强大的框架来识别因果遗传变异,并描述脓毒症易感性和临床结果的分子机制。方法:使用extreme将败血症GWAS汇总统计数据与来自基因型-组织表达版本8 (GTEx v8)项目的转录组学数据相结合,实施跨组织TWAS。候选基因通过互补的方法进行验证:FUSION、FOCUS和MAGMA。组织特异性和途径富集分析应用于脓毒症相关基因的优先排序,并表征其在疾病相关生物学过程中的功能作用。采用贝叶斯共定位和双样本孟德尔随机化(MR)分析来推断优先基因与脓毒症风险之间的推定因果关系。结果:4个基因zcchc4、PDGFB、C18orf54和atg4b在跨组织分析中显示出与脓毒症易感性的显著相关性。双样本MR为这些基因的基因调控表达对败血症风险的因果效应提供了证据。贝叶斯共定位确定了脓毒症相关位点和表达数量性状位点(eqtl)之间的共同因果变异,暗示了脓毒症发病机制中炎症和自噬途径的失调。结论:我们的研究结果强调了跨组织TWAS在定位败血症相关位点和阐明败血症易感性遗传结构方面的有效性。这些优先的基因座构成了功能验证的引人注目的靶点,并代表了脓毒症治疗干预的可行候选者。
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来源期刊
SHOCK
SHOCK 医学-外科
CiteScore
6.20
自引率
3.20%
发文量
199
审稿时长
1 months
期刊介绍: SHOCK®: Injury, Inflammation, and Sepsis: Laboratory and Clinical Approaches includes studies of novel therapeutic approaches, such as immunomodulation, gene therapy, nutrition, and others. The mission of the Journal is to foster and promote multidisciplinary studies, both experimental and clinical in nature, that critically examine the etiology, mechanisms and novel therapeutics of shock-related pathophysiological conditions. Its purpose is to excel as a vehicle for timely publication in the areas of basic and clinical studies of shock, trauma, sepsis, inflammation, ischemia, and related pathobiological states, with particular emphasis on the biologic mechanisms that determine the response to such injury. Making such information available will ultimately facilitate improved care of the traumatized or septic individual.
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