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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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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. |
format | Online Article Text |
id | pubmed-9263786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
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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