Coagulation dysfunction in COVID-19: The interplay between inflammation, viral infection and the coagulation system.


Journal

Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558

Informations de publication

Date de publication:
03 2021
Historique:
received: 31 03 2020
revised: 14 08 2020
accepted: 19 08 2020
pubmed: 2 9 2020
medline: 18 3 2021
entrez: 2 9 2020
Statut: ppublish

Résumé

COVID-19 is a new pandemic, caused by Severe Acute Respiratory Syndrome-CoronaVirus-2 (SARS-Cov2) infection and characterized by a broad spectrum of clinical manifestations. Inflammation and the innate immune system have been recently recognized as pivotal players in the most severe forms, characterized by significantly elevated levels of pro-inflammatory cytokines. In this setting, several studies have also reported the presence of abnormalities in coagulation parameters and platelets count, possibly identifying a subgroup of patients with poor prognosis. Some reports of full-blown thromboembolic events are emerging. Among the possible mechanisms underlying coagulation dysfunction, the so-called "cytokine storm" seems to play a pivotal role. Other candidate factors include virus-specific mechanisms, related to the virus interaction with renin angiotensin system (RAS) and the fibrinolytic pathway, but also comorbidities affecting these patients. Coagulation dysfunction is therefore a candidate risk factor for adverse outcomes in COVID-19 and should be carefully addressed in clinical practice.

Identifiants

pubmed: 32868115
pii: S0268-960X(20)30095-3
doi: 10.1016/j.blre.2020.100745
pmc: PMC7444609
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

100745

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

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Auteurs

Maria Grazia Lazzaroni (MG)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy. Electronic address: mariagrazialazzaroni@gmail.com.

Silvia Piantoni (S)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy. Electronic address: slv.piantoni@gmail.com.

Stefania Masneri (S)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy. Electronic address: stefania.masneri@libero.it.

Emirena Garrafa (E)

Department of Laboratory Diagnostics, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy. Electronic address: emirena.garrafa@unibs.it.

Giuliana Martini (G)

Hemostasis Central Laboratory, ASST Spedali Civili of Brescia, Brescia, Italy. Electronic address: giuliana.martini@asst-spedalicivili.it.

Angela Tincani (A)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy. Electronic address: angelatincani@gmail.com.

Laura Andreoli (L)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy. Electronic address: laura.andreoli@unibs.it.

Franco Franceschini (F)

Rheumatology and Clinical Immunology Unit, ASST Spedali Civili of Brescia, Brescia, Italy; Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy. Electronic address: franco.franceschini@unibs.it.

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Classifications MeSH