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Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming

BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global pandemic. Previous studies have reported dyslipidemia in patients with COVID-19. Herein, we conducted a retrospective study and a bioinformatics analysis to evaluate the essential data of the lipid profile as well as the possible mechanism...

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Autores principales: Zhao, Tie, Wang, Chunhui, Duan, Biyan, Yang, Peipei, Wu, Jianguo, Zhang, Qiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133671/
https://www.ncbi.nlm.nih.gov/pubmed/35633693
http://dx.doi.org/10.3389/fmicb.2022.863802
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author Zhao, Tie
Wang, Chunhui
Duan, Biyan
Yang, Peipei
Wu, Jianguo
Zhang, Qiwei
author_facet Zhao, Tie
Wang, Chunhui
Duan, Biyan
Yang, Peipei
Wu, Jianguo
Zhang, Qiwei
author_sort Zhao, Tie
collection PubMed
description BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global pandemic. Previous studies have reported dyslipidemia in patients with COVID-19. Herein, we conducted a retrospective study and a bioinformatics analysis to evaluate the essential data of the lipid profile as well as the possible mechanism in patients with COVID-19. METHODS: First of all, the retrospective study included three cohorts: patients with COVID-19, a healthy population, and patients with chronic obstructive pulmonary disease (COPD). For each subject, serum lipid profiles in the biochemical data were compared, including triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C). Furthermore, bioinformatics analyses were performed for exploring the biological or immunological mechanisms. RESULTS: In line with the biochemical data of the three cohorts, the statistical result displayed that patients with COVID-19 were more likely to have lower levels of TC and HDL-C as compared with healthy individuals. The differential proteins associated with COVID-19 are involved in the lipid pathway and can target and regulate cytokines and immune cells. Additionally, a heatmap revealed that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections were possibly involved in lipid metabolic reprogramming. The viral proteins, such as spike (S) and non-structural protein 2 (Nsp2) of SARS-CoV-2, may be involved in metabolic reprogramming. CONCLUSION: The metabolic reprogramming after SARS-CoV-2 infections is probably associated with the immune and clinical phenotype of patients. Hence, metabolic reprogramming may be targeted for developing antivirals against COVID-19.
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spelling pubmed-91336712022-05-27 Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming Zhao, Tie Wang, Chunhui Duan, Biyan Yang, Peipei Wu, Jianguo Zhang, Qiwei Front Microbiol Microbiology BACKGROUND: Coronavirus disease 2019 (COVID-19) is a global pandemic. Previous studies have reported dyslipidemia in patients with COVID-19. Herein, we conducted a retrospective study and a bioinformatics analysis to evaluate the essential data of the lipid profile as well as the possible mechanism in patients with COVID-19. METHODS: First of all, the retrospective study included three cohorts: patients with COVID-19, a healthy population, and patients with chronic obstructive pulmonary disease (COPD). For each subject, serum lipid profiles in the biochemical data were compared, including triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C). Furthermore, bioinformatics analyses were performed for exploring the biological or immunological mechanisms. RESULTS: In line with the biochemical data of the three cohorts, the statistical result displayed that patients with COVID-19 were more likely to have lower levels of TC and HDL-C as compared with healthy individuals. The differential proteins associated with COVID-19 are involved in the lipid pathway and can target and regulate cytokines and immune cells. Additionally, a heatmap revealed that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections were possibly involved in lipid metabolic reprogramming. The viral proteins, such as spike (S) and non-structural protein 2 (Nsp2) of SARS-CoV-2, may be involved in metabolic reprogramming. CONCLUSION: The metabolic reprogramming after SARS-CoV-2 infections is probably associated with the immune and clinical phenotype of patients. Hence, metabolic reprogramming may be targeted for developing antivirals against COVID-19. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9133671/ /pubmed/35633693 http://dx.doi.org/10.3389/fmicb.2022.863802 Text en Copyright © 2022 Zhao, Wang, Duan, Yang, Wu and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhao, Tie
Wang, Chunhui
Duan, Biyan
Yang, Peipei
Wu, Jianguo
Zhang, Qiwei
Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title_full Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title_fullStr Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title_full_unstemmed Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title_short Altered Lipid Profile in COVID-19 Patients and Metabolic Reprogramming
title_sort altered lipid profile in covid-19 patients and metabolic reprogramming
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133671/
https://www.ncbi.nlm.nih.gov/pubmed/35633693
http://dx.doi.org/10.3389/fmicb.2022.863802
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