A Genome-Wide Association Study of Serum Metabolite Profiles in Septic Shock Patients
CRITICAL CARE EXPLORATIONS(2024)
Abstract
OBJECTIVES:We sought to assess whether genetic associations with metabolite concentrations in septic shock patients could be used to identify pathways of potential importance for understanding sepsis pathophysiology.DESIGN:Retrospective multicenter cohort studies of septic shock patients.SETTING:All participants who were admitted to 27 participating hospital sites in three countries (Australia, New Zealand, and the United Kingdom) were eligible for inclusion.PATIENTS:Adult, critically ill, mechanically ventilated patients with septic shock (n = 230) who were a subset of the Adjunctive Corticosteroid Treatment in Critically Ill Patients with Septic Shock trial (ClinicalTrials.gov number: NCT01448109).INTERVENTIONS:None.MEASUREMENTS AND MAIN RESULTS:A genome-wide association study was conducted for a range of serum metabolite levels for participants. Genome-wide significant associations (p <= 5 x 10-8) were found for the two major ketone bodies (3-hydroxybutyrate [rs2456680] and acetoacetate [rs2213037] and creatinine (rs6851961). One of these single-nucleotide polymorphisms (SNPs) (rs2213037) was located in the alcohol dehydrogenase cluster of genes, which code for enzymes related to the metabolism of acetoacetate and, therefore, presents a plausible association for this metabolite. None of the three SNPs showed strong associations with risk of sepsis, 28- or 90-day mortality, or Acute Physiology and Chronic Health Evaluation score (a measure of sepsis severity).CONCLUSIONS:We suggest that the genetic associations with metabolites may reflect a starvation response rather than processes involved in sepsis pathophysiology. However, our results require further investigation and replication in both healthy and diseased cohorts including those of different ancestry.
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Key words
genetics,metabolomics,molecular biology,sepsis
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