The Plasma Lipidomic Landscape in Patients with Sepsis due to Community-acquired Pneumonia

dc.contributor.authorChouchane O.
dc.contributor.authorSchuurman A.R.
dc.contributor.authorReijnders T.D.Y.
dc.contributor.authorPeters-Sengers H.
dc.contributor.authorButler J.M.
dc.contributor.authorUhel F.
dc.contributor.authorSchultz M.J.
dc.contributor.authorBonten M.J.
dc.contributor.authorCremer O.L.
dc.contributor.authorCalfee C.S.
dc.contributor.authorMatthay M.A.
dc.contributor.authorLangley R.J.
dc.contributor.authorAlipanah-Lechner N.
dc.contributor.authorKingsmore S.F.
dc.contributor.authorRogers A.
dc.contributor.authorvan Weeghel M.
dc.contributor.authorVaz F.M.
dc.contributor.authorvan der Poll T.
dc.contributor.correspondenceChouchane O.
dc.contributor.otherMahidol University
dc.date.accessioned2024-04-25T18:14:21Z
dc.date.available2024-04-25T18:14:21Z
dc.date.issued2024-04-15
dc.description.abstractRationale: The plasma lipidome has the potential to reflect many facets of the host status during severe infection. Previous work is limited to specific lipid groups or was focused on lipids as prognosticators.Objectives: To map the plasma lipidome during sepsis due to community-acquired pneumonia (CAP) and determine the disease specificity and associations with clinical features.Methods: We analyzed 1,833 lipid species across 33 classes in 169 patients admitted to the ICU with sepsis due to CAP, 51 noninfected ICU patients, and 48 outpatient controls. In a paired analysis, we reanalyzed patients still in the ICU 4 days after admission (n = 82).Measurements and Main Results: A total of 58% of plasma lipids were significantly lower in patients with CAP-attributable sepsis compared with outpatient controls (6% higher, 36% not different). We found strong lipid class-specific associations with disease severity, validated across two external cohorts, and inflammatory biomarkers, in which triacylglycerols, cholesterol esters, and lysophospholipids exhibited the strongest associations. A total of 36% of lipids increased over time, and stratification by survival revealed diverging lipid recovery, which was confirmed in an external cohort; specifically, a 10% increase in cholesterol ester levels was related to a lower odds ratio (0.84; P = 0.006) for 30-day mortality (absolute mortality, 18 of 82). Comparison with noninfected ICU patients delineated a substantial common illness response (57.5%) and a distinct lipidomic signal for patients with CAP-attributable sepsis (37%).Conclusions: Patients with sepsis due to CAP exhibit a time-dependent and partially disease-specific shift in their plasma lipidome that correlates with disease severity and systemic inflammation and is associated with higher mortality.
dc.identifier.citationAmerican journal of respiratory and critical care medicine Vol.209 No.8 (2024) , 973-986
dc.identifier.doi10.1164/rccm.202308-1321OC
dc.identifier.eissn15354970
dc.identifier.pmid38240721
dc.identifier.scopus2-s2.0-85190754284
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/98102
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleThe Plasma Lipidomic Landscape in Patients with Sepsis due to Community-acquired Pneumonia
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85190754284&origin=inward
oaire.citation.endPage986
oaire.citation.issue8
oaire.citation.startPage973
oaire.citation.titleAmerican journal of respiratory and critical care medicine
oaire.citation.volume209
oairecerif.author.affiliationAmsterdam Gastroenterology Endocrinology Metabolism
oairecerif.author.affiliationMahidol Oxford Tropical Medicine Research Unit
oairecerif.author.affiliationEmma Kinderziekenhuis
oairecerif.author.affiliationUniversity of South Alabama College of Medicine
oairecerif.author.affiliationUniversity Medical Center Utrecht
oairecerif.author.affiliationUniversity of California, San Francisco
oairecerif.author.affiliationAP-HP Assistance Publique - Hopitaux de Paris
oairecerif.author.affiliationCNRS Centre National de la Recherche Scientifique
oairecerif.author.affiliationRady Children's Hospital
oairecerif.author.affiliationCenter for Experimental and Molecular Medicine
oairecerif.author.affiliationJulius Center for Health Sciences and Primary Care
oairecerif.author.affiliationCore Facility Metabolomics
oairecerif.author.affiliationLaboratory of Experimental Intensive Care and Anesthesiology
oairecerif.author.affiliationDivision of Infectious Diseases
oairecerif.author.affiliationDivision of Pulmonary and Critical Care Medicine

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