<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Morales-Ortiz J</submitter><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>2495-2505</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6284217</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>132(23)</volume><pubmed_abstract>Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) affect >200 000 individuals yearly with a 40% mortality rate. Although platelets are implicated in the progression of ALI/ARDS, their exact role remains undefined. Triggering receptor expressed in myeloid cells (TREM)-like transcript 1 (TLT-1) is found on platelets, binds fibrinogen, and mediates clot formation. We hypothesized that platelets use TLT-1 to manage the progression of ALI/ARDS. Here we retrospectively measure plasma levels of soluble TLT-1 (sTLT-1) from the ARDS Network clinical trial and show that patients whose sTLT-1 levels were >1200 pg/mL had nearly twice the mortality risk as those with &lt;1200 pg/mL (&lt;i>P&lt;/i> &lt; .001). After correcting for confounding factors such as creatinine levels, Acute Physiology </pubmed_abstract><journal>Blood</journal><pubmed_title>Platelet-derived TLT-1 is a prognostic indicator in ALI/ARDS and prevents tissue damage in the lungs in a mouse model.</pubmed_title><pmcid>PMC6284217</pmcid><funding_grant_id>SC2 GM081237</funding_grant_id><funding_grant_id>K01 GM103806</funding_grant_id><funding_grant_id>R01 HL090933</funding_grant_id><funding_grant_id>P20 GM103642</funding_grant_id><funding_grant_id>U54 MD007587</funding_grant_id><funding_grant_id>P20 GM103475</funding_grant_id><pubmed_authors>Ortiz-Zuazaga H</pubmed_authors><pubmed_authors>Rowley JW</pubmed_authors><pubmed_authors>Deal V</pubmed_authors><pubmed_authors>John AS</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Madera B</pubmed_authors><pubmed_authors>Maldonado-Martinez G</pubmed_authors><pubmed_authors>Croft C</pubmed_authors><pubmed_authors>Hunter R</pubmed_authors><pubmed_authors>Morales-Ortiz J</pubmed_authors><pubmed_authors>Reyes F</pubmed_authors><pubmed_authors>Ledesma N</pubmed_authors><pubmed_authors>Pacheco A</pubmed_authors><pubmed_authors>Lopez J</pubmed_authors><pubmed_authors>Rondina MT</pubmed_authors><pubmed_authors>Gibson A</pubmed_authors><pubmed_authors>Yost CC</pubmed_authors><pubmed_authors>Staback F</pubmed_authors><pubmed_authors>Washington AV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Platelet-derived TLT-1 is a prognostic indicator in ALI/ARDS and prevents tissue damage in the lungs in a mouse model.</name><description>Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) affect >200 000 individuals yearly with a 40% mortality rate. Although platelets are implicated in the progression of ALI/ARDS, their exact role remains undefined. Triggering receptor expressed in myeloid cells (TREM)-like transcript 1 (TLT-1) is found on platelets, binds fibrinogen, and mediates clot formation. We hypothesized that platelets use TLT-1 to manage the progression of ALI/ARDS. Here we retrospectively measure plasma levels of soluble TLT-1 (sTLT-1) from the ARDS Network clinical trial and show that patients whose sTLT-1 levels were >1200 pg/mL had nearly twice the mortality risk as those with &lt;1200 pg/mL (&lt;i>P&lt;/i> &lt; .001). After correcting for confounding factors such as creatinine levels, Acute Physiology </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Dec</publication><modification>2025-04-19T01:51:06.934Z</modification><creation>2021-02-20T20:03:56Z</creation></dates><accession>S-EPMC6284217</accession><cross_references><pubmed>30282800</pubmed><doi>10.1182/blood-2018-03-841593</doi></cross_references></HashMap>