Comprehensive analysis of immunogenic cell death-related gene and construction of prediction model based on WGCNA and multiple machine learning in severe COVID-19

Author:

Li Chunyu1,wu ke1,yang rui2,Liao Minghua1,Li Jun1,Zhu Qian1,Zhang Jiayi1,Zhang Xianming1

Affiliation:

1. Affiliated Hospital of Guizhou Medical University

2. The First People's Hospital of Guiyang

Abstract

Abstract Severe Acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) is a highly transmissible and pathogenic coronavirus that emerged in late 2019 and has caused a pandemic of acute respiratory disease with a high mortality rate. The death of coronavirus disease 2019 (COVID-19) is primarily due to from critically ill patients, especially from ARDS complications caused by SARS-CoV-2. Therefore, it is essential to contribute an in-depth understanding of the pathogenesis of the disease and to identify biomarkers for predicting critically ill patients at the molecular level, and thereby reduce COVID-19 mortality. Immunogenic cell death (ICD), as a specific variant of regulatory cell death driven by stress, can induce adaptive immune responses against cell death antigens in the host. Studies have confirmed that both innate and adaptive immune pathways are involved in the pathogenesis of SARS-CoV-2 infection. In severe COVID-19 patients, a large number of inflammatory mediators are released and cell death occurs, which leads to immune disorders. However, the role of ICD in the pathogenesis of severe COVID-19 has rarely been explored. In this study, we systematically evaluated the role of ICD-related genes in COVID-19. The differential expression of ICD-related genes in COVID-19 samples and healthy control samples, as well in ICU samples and Non-ICU samples were respectively explored. We conducted consensus clustering, immune infiltration analysis, and functional enrichment analysis based on ICD differentially expressed genes. The results showed that immune infiltration characteristics were altered in severe and non-severe COVID-19. In addition, we used multiple machine learning methods to screen for five risk genes (KLF5, BICDL1, APH1B, GRB10, and OLAH), which are used to predict COVID-19 severity. Finally, we constructed a nomogram to predict the risk of severe COVID-19 based on the classification and recognition model, and validated the model with external data sets. This study provides a valuable direction for the exploration of the pathogenesis and progress of COVID-19, and helps in the early identification of severe cases of COVID-19 to reduce mortality.

Publisher

Research Square Platform LLC

Reference47 articles.

1. World Health Organization (WHO). (2023) Coronavirus disease (COVID-19) Weekly Epidemiological Updates and Monthly Operational Updates.https://www.who.int/emergencies/diseases/novel-coronavirus-2019/ situation-reports. Accessed 16th March 2023.

2. Clinical course and predictors of 60-day mortality in 239 critically ill patients with COVID-19: a multicenter retrospective study from Wuhan, China;Xu J;Crit Care,2020

3. Gao Y. COVID-19: Risk factors for critical illness. EClinicalMedicine. 2020. 25: 100507.

4. Factors associated with hospital admission and critical illness among 5279 people with coronavirus disease 2019 in New York City: prospective cohort study;Petrilli CM;BMJ,2020

5. Postmortem examination of COVID-19 patients reveals diffuse alveolar damage with severe capillary congestion and variegated findings in lungs and other organs suggesting vascular dysfunction;Menter T;Histopathology,2020

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3