<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>116(4)</volume><submitter>Philippe A</submitter><funding>Agence Nationale de la Recherche</funding><funding>Fondation de France</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Coronavirus disease 2019 (COVID-19) is associated with an inflammatory cytokine burst and a prothrombotic coagulopathy. Platelets may contribute to microthrombosis, and constitute a therapeutic target in COVID-19 therapy.&lt;h4>Aim&lt;/h4>To assess if platelet activation influences mortality in COVID-19.&lt;h4>Methods&lt;/h4>We explored two cohorts of patients with COVID-19. Cohort A included 208 ambulatory and hospitalized patients with varying clinical severities and non-COVID patients as controls, in whom plasma concentrations of the soluble platelet activation biomarkers CD40 ligand (sCD40L) and P-selectin (sP-sel) were quantified within the first 48hours following hospitalization. Cohort B was a multicentre cohort of 2878 patients initially admitted to a medical ward. In both c</pubmed_abstract><journal>Archives of cardiovascular diseases</journal><pagination>183-191</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9925415</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Platelet activation and coronavirus disease 2019 mortality: Insights from coagulopathy, antiplatelet therapy and inflammation.</pubmed_title><pmcid>PMC9925415</pmcid><pubmed_authors>Sanchez O</pubmed_authors><pubmed_authors>Fauvel C</pubmed_authors><pubmed_authors>Planquette B</pubmed_authors><pubmed_authors>Mirault T</pubmed_authors><pubmed_authors>Smadja DM</pubmed_authors><pubmed_authors>Weizman O</pubmed_authors><pubmed_authors>Chocron R</pubmed_authors><pubmed_authors>Samama CM</pubmed_authors><pubmed_authors>Philippe A</pubmed_authors><pubmed_authors>Waldmann V</pubmed_authors><pubmed_authors>Cohen A</pubmed_authors><pubmed_authors>Gaussem P</pubmed_authors><pubmed_authors>Hadjadj J</pubmed_authors><pubmed_authors>Guerin CL</pubmed_authors><pubmed_authors>Gendron N</pubmed_authors><pubmed_authors>Terrier B</pubmed_authors><pubmed_authors>Bonnet G</pubmed_authors><pubmed_authors>Hauw-Berlemont C</pubmed_authors><pubmed_authors>Fontenay M</pubmed_authors><pubmed_authors>Sutter W</pubmed_authors><pubmed_authors>Yatim N</pubmed_authors><pubmed_authors>Diehl JL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Platelet activation and coronavirus disease 2019 mortality: Insights from coagulopathy, antiplatelet therapy and inflammation.</name><description>&lt;h4>Background&lt;/h4>Coronavirus disease 2019 (COVID-19) is associated with an inflammatory cytokine burst and a prothrombotic coagulopathy. Platelets may contribute to microthrombosis, and constitute a therapeutic target in COVID-19 therapy.&lt;h4>Aim&lt;/h4>To assess if platelet activation influences mortality in COVID-19.&lt;h4>Methods&lt;/h4>We explored two cohorts of patients with COVID-19. Cohort A included 208 ambulatory and hospitalized patients with varying clinical severities and non-COVID patients as controls, in whom plasma concentrations of the soluble platelet activation biomarkers CD40 ligand (sCD40L) and P-selectin (sP-sel) were quantified within the first 48hours following hospitalization. Cohort B was a multicentre cohort of 2878 patients initially admitted to a medical ward. In both c</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-05T11:43:37.792Z</modification><creation>2025-02-18T22:34:12.25Z</creation></dates><accession>S-EPMC9925415</accession><cross_references><pubmed>36858909</pubmed><doi>10.1016/j.acvd.2023.01.006</doi></cross_references></HashMap>