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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.
  • Gan YH; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Ou YN; Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
  • Yang YX; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Deng YT; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Liu Y; Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
  • Tan L; Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
  • Yu JT; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Ann Transl Med ; 10(11): 624, 2022 Jun.
Article in English | MEDLINE | ID: covidwho-1918239
ABSTRACT

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.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Etiology study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Ann Transl Med Year: 2022 Document Type: Article Affiliation country: Atm-21-6612

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Etiology study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal: Ann Transl Med Year: 2022 Document Type: Article Affiliation country: Atm-21-6612