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通过多性状全基因组关联研究分析探索与新冠病毒疾病严重程度和免疫反应相关的基因位点。

Exploring genetic loci linked to COVID-19 severity and immune response through multi-trait GWAS analyses.

作者信息

Meng Ziang, Zhang Chumeng, Liu Shuai, Li Wen, Wang Yue, Zhang Qingyi, Peng Bichen, Ye Weiyi, Jiang Yue, Song Yingchao, Guo Miao, Chang Xiao, Shao Lei

机构信息

Department of Infectious Disease, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

The Second School of Clinical Medicine of Shandong First Medical University, Tai'an, Shandong, China.

出版信息

Front Genet. 2025 Feb 17;16:1502839. doi: 10.3389/fgene.2025.1502839. eCollection 2025.

Abstract

INTRODUCTION

COVID-19 severity has been linked to immune factors, with excessive immune responses like cytokine storms contributing to mortality. However, the genetic basis of these immune responses is not well understood. This study aimed to explore the genetic connection between COVID-19 severity and blood cell traits, given their close relationship with immunity.

MATERIALS AND METHODS

GWAS summary statistics for COVID-19 and blood cell counts were analyzed using Linkage Disequilibrium Score Regression (LDSC) to estimate genetic correlations and heritabilities. For traits with significant correlations, a Multi-Trait GWAS Analysis (MTAG) was performed to identify pleiotropic loci shared between COVID-19 and blood cell counts.

RESULTS

Our MTAG analysis identified four pleiotropic loci associated with COVID-19 severity, five loci linked to hospitalized cases, and one locus related to general patients. Among these, two novel loci were identified in the high-risk population, with rs55779981 located near and rs73009538 near . In hospitalized patients, two previously unrecognized loci were detected, namely, rs115545251 near and rs3181049 near , while in general patients, rs11065822 near emerged as a newly identified locus. We also identified potential target genes, including those involved in inflammation signaling (), endothelial dysfunction (), and antiviral immune response (), which may require further investigation.

CONCLUSION

Our study offers insights into the genetic overlap between COVID-19 and immune factors, suggesting potential directions for future research and clinical exploration.

摘要

引言

新冠病毒病(COVID-19)的严重程度与免疫因素有关,细胞因子风暴等过度免疫反应会导致死亡。然而,这些免疫反应的遗传基础尚不清楚。鉴于血细胞特征与免疫力密切相关,本研究旨在探讨COVID-19严重程度与血细胞特征之间的遗传联系。

材料与方法

使用连锁不平衡评分回归(LDSC)分析COVID-19和血细胞计数的全基因组关联研究(GWAS)汇总统计数据,以估计遗传相关性和遗传力。对于具有显著相关性的性状,进行多性状GWAS分析(MTAG),以识别COVID-19和血细胞计数之间共享的多效性位点。

结果

我们的MTAG分析确定了4个与COVID-19严重程度相关的多效性位点、5个与住院病例相关的位点和1个与普通患者相关的位点。其中,在高危人群中发现了2个新位点,rs55779981位于 附近,rs73009538位于 附近。在住院患者中,检测到2个以前未被识别的位点,即 附近的rs115545251和 附近的rs3181049,而在普通患者中, 附近的rs11065822是一个新发现的位点。我们还确定了潜在的靶基因,包括参与炎症信号传导()、内皮功能障碍()和抗病毒免疫反应()的基因,这些基因可能需要进一步研究。

结论

我们的研究揭示了COVID-19与免疫因素之间的遗传重叠,为未来的研究和临床探索提供了潜在的方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4536/11873281/ecb6d71488a5/fgene-16-1502839-g001.jpg

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