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Investigation of the Molecular Mechanism of Coagulopathy in Severe and Critical Patients With COVID-19.
- Source :
-
Frontiers in immunology [Front Immunol] 2021 Dec 16; Vol. 12, pp. 762782. Date of Electronic Publication: 2021 Dec 16 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- Coagulopathy is a frequently reported finding in the pathology of coronavirus disease 2019 (COVID-19); however, the molecular mechanism, the involved coagulation factors, and the role of regulatory proteins in homeostasis are not fully investigated. We explored the dynamic changes of nine coagulation tests in patients and controls to propose a molecular mechanism for COVID-19-associated coagulopathy. Coagulation tests including prothrombin time (PT), partial thromboplastin time (PTT), fibrinogen (FIB), lupus anticoagulant (LAC), proteins C and S, antithrombin III (ATIII), D-dimer, and fibrin degradation products (FDPs) were performed on plasma collected from 105 individuals (35 critical patients, 35 severe patients, and 35 healthy controls). There was a statically significant difference when the results of the critical (CRT) and/or severe (SVR) group for the following tests were compared to the control (CRL) group: PT <subscript>CRT</subscript> (15.014) and PT <subscript>SVR</subscript> (13.846) (PT <subscript>CRL</subscript>  = 13.383, p  < 0.001), PTT <subscript>CRT</subscript> (42.923) and PTT <subscript>SVR</subscript> (37.8) (PTT <subscript>CRL</subscript>  = 36.494, p  < 0.001), LAC <subscript>CRT</subscript> (49.414) and LAC <subscript>SVR</subscript> (47.046) (LAC <subscript>CRL</subscript>  = 40.763, p  < 0.001), FIB <subscript>CRT</subscript> (537.66) and FIB <subscript>SVR</subscript> (480.29) (FIB <subscript>CRL</subscript>  = 283.57, p  < 0.001), ProC <subscript>CRT</subscript> (85.57%) and ProC <subscript>SVR</subscript> (99.34%) (ProC <subscript>CRL</subscript>  = 94.31%, p  = 0.04), ProS <subscript>CRT</subscript> (62.91%) and ProS <subscript>SVR</subscript> (65.06%) (ProS <subscript>CRL</subscript>  = 75.03%, p  < 0.001), D-dimer ( p  < 0.0001, χ <superscript>2</superscript>  = 34.812), and FDP ( p  < 0.002, χ <superscript>2</superscript>  = 15.205). No significant association was found in the ATIII results in groups (ATIII <subscript>CRT</subscript>  = 95.71% and ATIII <subscript>SVR</subscript>  = 99.63%; ATIII <subscript>CRL</subscript>  = 98.74%, p  = 0.321). D-dimer, FIB, PT, PTT, LAC, protein S, FDP, and protein C (ordered according to p -values) have significance in the prognosis of patients. Disruptions in homeostasis in protein C (and S), VIII/VIIIa and V/Va axes, probably play a role in COVID-19-associated coagulopathy.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Elieh Ali Komi, Rahimi, Asghari, Jafari, Rasouli, Mohebalizadeh, Abbasi, Nejadrahim, Rezazadeh and Shafiei-Irannejad.)
- Subjects :
- Adult
Aged
Blood Coagulation Disorders complications
Blood Coagulation Disorders diagnosis
Blood Coagulation Factors metabolism
COVID-19 virology
Female
Fibrin metabolism
Fibrin Fibrinogen Degradation Products metabolism
Homeostasis
Humans
Male
Middle Aged
Partial Thromboplastin Time
Prognosis
Protein C metabolism
Prothrombin Time
SARS-CoV-2 genetics
SARS-CoV-2 physiology
Blood Coagulation
Blood Coagulation Disorders blood
Blood Coagulation Tests methods
COVID-19 complications
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 34975853
- Full Text :
- https://doi.org/10.3389/fimmu.2021.762782