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A Chinese host genetic study discovered IFNs and causality of laboratory traits on COVID-19 severity

The COVID-19 pandemic has caused over 220 million infections and 4.5 million deaths worldwide. Current risk factor cannot fully explain the diversity in disease severity. Here, we present a comprehensive analysis of a broad range of patients' laboratory and clinical assessments to investigate t...

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Detalles Bibliográficos
Autores principales: Zhu, Huanhuan, Zheng, Fang, Li, Linxuan, Jin, Yan, Luo, Yuxue, Li, Zhen, Zeng, Jingyu, Tang, Ling, Li, Zilong, Xia, Ningyu, Liu, Panhong, Han, Dan, Shan, Ying, Zhu, Xiaoying, Liu, Siyang, Xie, Rong, Chen, Yilin, Liu, Wen, Liu, Longqi, Xu, Xun, Wang, Jian, Yang, Huanming, Shen, Xia, Jin, Xin, Cheng, Fanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481128/
https://www.ncbi.nlm.nih.gov/pubmed/34608450
http://dx.doi.org/10.1016/j.isci.2021.103186
Descripción
Sumario:The COVID-19 pandemic has caused over 220 million infections and 4.5 million deaths worldwide. Current risk factor cannot fully explain the diversity in disease severity. Here, we present a comprehensive analysis of a broad range of patients' laboratory and clinical assessments to investigate the genetic contributions to COVID-19 severity. By performing GWAS analysis, we discovered several concrete associations for laboratory traits and used Mendelian randomization (MR) analysis to further investigate the causality of traits on disease severity. Two causal traits, WBC counts and cholesterol levels, were identified based on MR study, and their functional genes are located at genes MHC complex and ApoE, respectively. Our gene-based analysis and GSEA revealed four interferon pathways, including type I interferon receptor binding and SARS coronavirus and innate immunity. We hope that our work will contribute to studying the genetic mechanisms of disease and serve as a useful reference for COVID-19 diagnosis and treatment.