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Identification of novel drug targets for the risk and prognosis of COVID-19

BACKGROUND: Since the epidemic continues, there is a pressing need to improve our understanding of coronavirus disease 2019 (COVID-19). Mendelian randomization (MR) studies provide us with a method to explore the causality between circulating proteins and COVID-19 susceptibility and severity. We aim...

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Autores principales: Gan, Yi-Han, Ou, Ya-Nan, Yang, Yu-Xiang, Deng, Yue-Ting, Liu, Yi, Tan, Lan, Yu, Jin-Tai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263786/
https://www.ncbi.nlm.nih.gov/pubmed/35813330
http://dx.doi.org/10.21037/atm-21-6612
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author Gan, Yi-Han
Ou, Ya-Nan
Yang, Yu-Xiang
Deng, Yue-Ting
Liu, Yi
Tan, Lan
Yu, Jin-Tai
author_facet Gan, Yi-Han
Ou, Ya-Nan
Yang, Yu-Xiang
Deng, Yue-Ting
Liu, Yi
Tan, Lan
Yu, Jin-Tai
author_sort Gan, Yi-Han
collection PubMed
description BACKGROUND: Since the epidemic continues, there is a pressing need to improve our understanding of coronavirus disease 2019 (COVID-19). Mendelian randomization (MR) studies provide us with a method to explore the causality between circulating proteins and COVID-19 susceptibility and severity. We aim to find new perspectives on the pathological mechanism of the disease and possible drug targets for treatment based on this study. METHODS: We conducted a phenome-wide MR study to prioritize circulating proteins causally associated with COVID-19 susceptibility, which was defined as “patients tested positive for COVID-19 vs. population controls”, and severity, which was defined as “patients hospitalized with COVID-19 vs. population controls”. And we repeated the analysis for different definition of COVID-19 susceptibility, severity and control groups. RESULTS: Association of three circulating proteins with COVID-19 susceptibility and severity were demonstrated via our study. C-C motif chemokine 4 (OR =1.887, 95% CI: 1.608–2.165, P=8.04×10(−6)) and 2'-5'-oligoadenylate synthase 1 (OR =0.511, 95% CI: 0.266–0.757, P=8.51×10(−8)) were found respectively positively and negatively correlated with increased COVID-19 severity. Tissue factor, contrary to previous studies, was found associated with decreased COVID-19 susceptibility (OR =0.667, 95% CI: 0.484–0.850, P=1.47×10(−5)) and decreased COVID-19 severity (OR =0.459, 95% CI: 0.132–0.786, P=3.01×10(−6)). CONCLUSIONS: Genetic evidence supports C-C motif chemokine 4 as a risk factor for COVID-19 severity, and 2'-5'-oligoadenylate synthase 1 as a protective factor for COVID-19 severity. The causal association between tissue factor and COVID-19 is contrary to the previous studies, needing further analyses. Further research is warranted to assess the viability of C-C motif chemokine 4 and 2'-5'-oligoadenylate synthase 1 as well as their downstream pathways as drug targets for anti-inflammatory and anti-virus treatment in severe cases.
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spelling pubmed-92637862022-07-09 Identification of novel drug targets for the risk and prognosis of COVID-19 Gan, Yi-Han Ou, Ya-Nan Yang, Yu-Xiang Deng, Yue-Ting Liu, Yi Tan, Lan Yu, Jin-Tai Ann Transl Med Original Article BACKGROUND: Since the epidemic continues, there is a pressing need to improve our understanding of coronavirus disease 2019 (COVID-19). Mendelian randomization (MR) studies provide us with a method to explore the causality between circulating proteins and COVID-19 susceptibility and severity. We aim to find new perspectives on the pathological mechanism of the disease and possible drug targets for treatment based on this study. METHODS: We conducted a phenome-wide MR study to prioritize circulating proteins causally associated with COVID-19 susceptibility, which was defined as “patients tested positive for COVID-19 vs. population controls”, and severity, which was defined as “patients hospitalized with COVID-19 vs. population controls”. And we repeated the analysis for different definition of COVID-19 susceptibility, severity and control groups. RESULTS: Association of three circulating proteins with COVID-19 susceptibility and severity were demonstrated via our study. C-C motif chemokine 4 (OR =1.887, 95% CI: 1.608–2.165, P=8.04×10(−6)) and 2'-5'-oligoadenylate synthase 1 (OR =0.511, 95% CI: 0.266–0.757, P=8.51×10(−8)) were found respectively positively and negatively correlated with increased COVID-19 severity. Tissue factor, contrary to previous studies, was found associated with decreased COVID-19 susceptibility (OR =0.667, 95% CI: 0.484–0.850, P=1.47×10(−5)) and decreased COVID-19 severity (OR =0.459, 95% CI: 0.132–0.786, P=3.01×10(−6)). CONCLUSIONS: Genetic evidence supports C-C motif chemokine 4 as a risk factor for COVID-19 severity, and 2'-5'-oligoadenylate synthase 1 as a protective factor for COVID-19 severity. The causal association between tissue factor and COVID-19 is contrary to the previous studies, needing further analyses. Further research is warranted to assess the viability of C-C motif chemokine 4 and 2'-5'-oligoadenylate synthase 1 as well as their downstream pathways as drug targets for anti-inflammatory and anti-virus treatment in severe cases. AME Publishing Company 2022-06 /pmc/articles/PMC9263786/ /pubmed/35813330 http://dx.doi.org/10.21037/atm-21-6612 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Gan, Yi-Han
Ou, Ya-Nan
Yang, Yu-Xiang
Deng, Yue-Ting
Liu, Yi
Tan, Lan
Yu, Jin-Tai
Identification of novel drug targets for the risk and prognosis of COVID-19
title Identification of novel drug targets for the risk and prognosis of COVID-19
title_full Identification of novel drug targets for the risk and prognosis of COVID-19
title_fullStr Identification of novel drug targets for the risk and prognosis of COVID-19
title_full_unstemmed Identification of novel drug targets for the risk and prognosis of COVID-19
title_short Identification of novel drug targets for the risk and prognosis of COVID-19
title_sort identification of novel drug targets for the risk and prognosis of covid-19
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9263786/
https://www.ncbi.nlm.nih.gov/pubmed/35813330
http://dx.doi.org/10.21037/atm-21-6612
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