Plasma lipidomic signatures reveal age-associated patterns of septic shock risk and immune dysregulation in sepsis
Bibliographic record
Abstract
Background: Sepsis is associated with significant lipidomic disturbances, but age-associated lipidomic patterns remain poorly characterized. Given the links between aging, immune dysfunction, and metabolic dysregulation, defining age-specific lipid profiles could improve sepsis risk assessment. This study investigates age-stratified lipidomic signatures in sepsis and identifies biomarkers for clinical severity. Methods: We prospectively enrolled 62 sepsis patients (21 <65 years, 41 ≥65 years) and 40 healthy controls. Plasma lipidomics was performed via untargeted LC-MS/MS, identifying 1,277 lipid species across 38 subclasses. Principal component analysis (PCA) and consensus clustering were used to assess lipidomic differences and define patient subtypes. Correlations between lipid subclasses, clinical severity (SOFA scores), and immune cell subsets were analyzed. An age-adjusted risk stratification model was developed to assess septic shock and mortality risk (AUC analysis). Results: Sepsis patients exhibited reduced phosphatidylcholine (PC), cholesteryl ester (CE), and lysophosphatidylcholine (LPC) levels (all P<0.05). Clustering revealed four lipidomic patterns, with Cluster 4 distinguishing two sepsis subtypes (C1, C2). Subtype C2 had higher septic shock incidence (57.1% vs. 14.8%, P = 0.0013) and downregulation of 92 lipids, 35 of which strongly correlated with SOFA scores. A risk stratification model incorporating six key lipids (LPC(19:0), PC(P-19:0), SM 32:3;2O(FA 16:3), PC(P-20:0), PC(O-18:1/20:3), CE(15:0)) and age accurately predicted septic shock (AUC: 0.87 training, 0.82 validation) and mortality risk in elderly patients. PC levels correlated with monocytes, while CE and LPC associated with complement proteins and CD8+ T cells. Conclusions: Our lipid-based model effectively predicts septic shock and mortality, particularly in elderly sepsis patients. Age-associated lipid alterations (PC, LPC, CE reduction) correlate with disease severity and immune dysregulation, suggesting distinct lipid-immune mechanisms in younger vs. elderly patients. These findings support lipidomics as a tool for sepsis risk stratification and personalized therapy.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.001 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.001 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".