Plasma Metabolites in Early Sepsis Identify Distinct Clusters Defined by Plasma Lipids. (29th July 2021)

• Record Type: Journal Article
• Authors: Rogers, Angela J.; Leligdowicz, Aleksandra; Contrepois, Kévin; Jauregui, Alejandra; Vessel, Kathryn; Deiss, Thomas J.; Belzer, Annika; Liu, Tom; Lippi, Matthew; Ke, Serena; Ross, Erin; Zhou, Hanjing; Hendrickson, Carolyn; Gomez, Antonio; Sinha, Pratik; Kangelaris, Kirsten N.; Liu, Kathleen D.; Calfee, Carolyn S.; Matthay, Michael A.
• Is Part Of: Critical care explorations. Volume 3:Number 8(2021)
• Page Start: e0478
• Publication Date: 2021-07-29
• Subjects: acute respiratory distress syndrome -- clustering -- metabolomics -- phenotype -- sepsis
• DOI: 10.1097/CCE.0000000000000478
• Languages: English
• ISSNs: 2639-8028

Abstract

Abstract : Supplemental Digital Content is available in the text. Abstract : OBJECTIVES: Unbiased global metabolomic profiling has not been used to identify distinct subclasses in patients with early sepsis and sepsis-associated acute respiratory distress syndrome. In this study, we examined whether the plasma metabolome reflects systemic illness in early sepsis and in acute respiratory distress syndrome. DESIGN: Plasma metabolites were measured in subjects with early sepsis. SETTING: Patients were admitted from the emergency department to the ICU in a plasma sample collected within 24 hours of ICU admission. Metabolic profiling of 970 metabolites was performed by Metabolon (Durham, NC). Hierarchical clustering and partial least squares discriminant clustering were used to identify distinct clusters among patients with early sepsis and sepsis-associated acute respiratory distress syndrome. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Among critically ill patients with early sepsis ( n = 197), three metabolically distinct subgroups were identified, with metabolic subtype driven by plasma lipids. Group 1, with 45 subjects (23% of cohort), had increased 60-day mortality (odds ratio, 2; 95% CI, 0.99–4.0; p = 0.04 for group 1 vs all others). This group also had higher rates of vasopressor-dependent shock, acute kidney injury, and met Berlin acute respiratory distress syndrome criteria more often (all p < 0.05). Conversely, metabolic group 3, with 76 subjects (39% of cohort), had the lowest risk of 60-day mortality (odds ratio, 0.44; 95% CI, 0.22–0.86; p = 0.01) and lower rates of organ dysfunction as reflected in a lower Simplified Acute Physiology Score II ( p < 0.001). In contrast, global metabolomic profiling did not separate patient with early sepsis with moderate-to-severe acute respiratory distress syndrome ( n = 78) from those with sepsis without acute respiratory distress syndrome ( n = 75). CONCLUSIONS: Plasma metabolomic profiling in patients with early sepsis identified three metabolically distinct groups that were characterized by different plasma lipid profiles, distinct clinical phenotypes, and 60-day mortality. Plasma metabolites did not distinguish patients with early sepsis who developed acute respiratory distress syndrome from those who did not.