<HashMap><database>biostudies-literature</database><scores/><additional><submitter>LaCroix IS</submitter><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>e1299-e1312</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10728352</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>278(6)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Advanced mass spectrometry methods were leveraged to analyze both proteomics and metabolomics signatures in plasma upon controlled tissue injury (TI) and hemorrhagic shock (HS)-isolated or combined-in a swine model, followed by correlation to viscoelastic measurements of coagulopathy via thrombelastography.&lt;h4>Background&lt;/h4>TI and HS cause distinct molecular changes in plasma in both animal models and trauma patients. However, the contribution to coagulopathy of trauma, the leading cause of preventable mortality in this patient population remains unclear. The recent development of a swine model for isolated or combined TI+HS facilitated the current study.&lt;h4>Methods&lt;/h4>Male swine (n=17) were randomized to either isolated or combined TI and HS. Coagulation status was ana</pubmed_abstract><journal>Annals of surgery</journal><pubmed_title>Omics Signatures of Tissue Injury and Hemorrhagic Shock in Swine.</pubmed_title><pmcid>PMC10728352</pmcid><funding_grant_id>R01 HL146442</funding_grant_id><funding_grant_id>T32 GM008315</funding_grant_id><funding_grant_id>R01 HL161004</funding_grant_id><funding_grant_id>R01 HL149714</funding_grant_id><funding_grant_id>R01 HL148151</funding_grant_id><funding_grant_id>RM1 GM131968</funding_grant_id><pubmed_authors>Silliman C</pubmed_authors><pubmed_authors>D'Alessandro A</pubmed_authors><pubmed_authors>Dzieciatkowska M</pubmed_authors><pubmed_authors>Cohen M</pubmed_authors><pubmed_authors>LaCroix IS</pubmed_authors><pubmed_authors>Moore EE</pubmed_authors><pubmed_authors>Cendali FI</pubmed_authors><pubmed_authors>Hom P</pubmed_authors><pubmed_authors>Hansen KC</pubmed_authors><pubmed_authors>Mitra S</pubmed_authors><pubmed_authors>Sauaia A</pubmed_authors><pubmed_authors>Cralley A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Omics Signatures of Tissue Injury and Hemorrhagic Shock in Swine.</name><description>&lt;h4>Objective&lt;/h4>Advanced mass spectrometry methods were leveraged to analyze both proteomics and metabolomics signatures in plasma upon controlled tissue injury (TI) and hemorrhagic shock (HS)-isolated or combined-in a swine model, followed by correlation to viscoelastic measurements of coagulopathy via thrombelastography.&lt;h4>Background&lt;/h4>TI and HS cause distinct molecular changes in plasma in both animal models and trauma patients. However, the contribution to coagulopathy of trauma, the leading cause of preventable mortality in this patient population remains unclear. The recent development of a swine model for isolated or combined TI+HS facilitated the current study.&lt;h4>Methods&lt;/h4>Male swine (n=17) were randomized to either isolated or combined TI and HS. Coagulation status was ana</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-18T16:51:59.825Z</modification><creation>2025-04-07T04:19:25.228Z</creation></dates><accession>S-EPMC10728352</accession><cross_references><pubmed>37334680</pubmed><doi>10.1097/SLA.0000000000005944</doi><doi>10.1097/sla.0000000000005944</doi></cross_references></HashMap>