<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Augustin B</submitter><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>431</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11667828</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Lipids play a critical role in defense against sepsis. We sought to investigate gene expression and lipidomic patterns of lipid dysregulation in sepsis.&lt;h4>Methods&lt;/h4>Data from four adult sepsis studies were analyzed and findings were investigated in two external datasets. Previously characterized lipid dysregulation subphenotypes of hypolipoprotein (HYPO; low lipoproteins, increased mortality) and normolipoprotein (NORMO; higher lipoproteins, lower mortality) were studied. Leukocytes collected within 24 h of sepsis underwent RNA sequencing (RNAseq) and shotgun plasma lipidomics was performed.&lt;h4>Results&lt;/h4>Of 288 included patients, 43% were HYPO and 57% were NORMO. HYPO patients exhibited higher median SOFA scores (9 vs 5, p = &lt; 0.001), vasopressor use (67% vs 34%, p </pubmed_abstract><journal>Critical care (London, England)</journal><pubmed_title>Multiomic molecular patterns of lipid dysregulation in a subphenotype of sepsis with higher shock incidence and mortality.</pubmed_title><pmcid>PMC11667828</pmcid><funding_grant_id>R01 GM133815</funding_grant_id><funding_grant_id>R35HL150784</funding_grant_id><funding_grant_id>R01HL162124</funding_grant_id><funding_grant_id>R01CA265907</funding_grant_id><funding_grant_id>K23 GM144802</funding_grant_id><funding_grant_id>K08GM151392</funding_grant_id><funding_grant_id>K12HL133304</funding_grant_id><funding_grant_id>K08 GM151392</funding_grant_id><funding_grant_id>R35 HL150784</funding_grant_id><funding_grant_id>R01GM133815</funding_grant_id><funding_grant_id>R01 HL162124</funding_grant_id><funding_grant_id>R01 CA265907</funding_grant_id><funding_grant_id>K12 HL133304</funding_grant_id><funding_grant_id>K23GM144802</funding_grant_id><pubmed_authors>Sulaiman D</pubmed_authors><pubmed_authors>Cagmat E</pubmed_authors><pubmed_authors>Hopson C</pubmed_authors><pubmed_authors>Labilloy G</pubmed_authors><pubmed_authors>Augustin B</pubmed_authors><pubmed_authors>Reddy ST</pubmed_authors><pubmed_authors>Wu D</pubmed_authors><pubmed_authors>Smith L</pubmed_authors><pubmed_authors>Graim K</pubmed_authors><pubmed_authors>Jacob V</pubmed_authors><pubmed_authors>Bertrand A</pubmed_authors><pubmed_authors>Hofmaenner DA</pubmed_authors><pubmed_authors>Datta S</pubmed_authors><pubmed_authors>Guirgis FW</pubmed_authors><pubmed_authors>Black LP</pubmed_authors><pubmed_authors>Shavit JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiomic molecular patterns of lipid dysregulation in a subphenotype of sepsis with higher shock incidence and mortality.</name><description>&lt;h4>Background&lt;/h4>Lipids play a critical role in defense against sepsis. We sought to investigate gene expression and lipidomic patterns of lipid dysregulation in sepsis.&lt;h4>Methods&lt;/h4>Data from four adult sepsis studies were analyzed and findings were investigated in two external datasets. Previously characterized lipid dysregulation subphenotypes of hypolipoprotein (HYPO; low lipoproteins, increased mortality) and normolipoprotein (NORMO; higher lipoproteins, lower mortality) were studied. Leukocytes collected within 24 h of sepsis underwent RNA sequencing (RNAseq) and shotgun plasma lipidomics was performed.&lt;h4>Results&lt;/h4>Of 288 included patients, 43% were HYPO and 57% were NORMO. HYPO patients exhibited higher median SOFA scores (9 vs 5, p = &lt; 0.001), vasopressor use (67% vs 34%, p </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-01T23:06:11.974Z</modification><creation>2025-04-06T17:36:08.327Z</creation></dates><accession>S-EPMC11667828</accession><cross_references><pubmed>39716214</pubmed><doi>10.1186/s13054-024-05216-3</doi></cross_references></HashMap>