Plasma Ceramides Levels in Severe COVID-19 Disease: Correlations with Survival

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Authors: Tri Pham, Andrea M Heredia Castillo, Andrew Atkinson, Linda R. Peterson, Cristina Vazquez Guillamet
Cited by: 0
References: 62

Abstract

Background: Dysregulated inflammatory processes have been associated with severe COVID-19 disease. Ceramides, bioactive lipids involved in inflammatory signaling, have been utilized to predict outcomes in chronic cardiometabolic diseases and pancreatic cancer, but their role in COVID-19 remains unknown. Methods: This observational study prospectively enrolled patients with COVID-19 disease who required intubation and mechanical ventilation at a Midwestern academic hospital between August 2020 and March 2021. Plasma ceramides 16:0 (C16), 22:0 (C22), and 24:0 (C24) and inflammatory markers (CRP, ESR, D-Dimer, and ferritin) were collected and organized weekly from symptom onset for up to 6 weeks. Patients were grouped by in-hospital mortality status. Linear mixed-effects models assessed temporal trends and associations between ceramides, inflammatory markers, and clinical outcomes. Results: = .04). C16, C22, and C24 followed similar temporal trajectories to each other, but demonstrated an inverse pattern when compared with other inflammatory markers. Nonsurvivors demonstrated higher plasma levels of all the ceramide species in the first week of illness, followed by lower levels compared with survivors in subsequent weeks. Conclusions: The synchronous trajectories of C16, C22, and C24 differ from patterns reported in chronic disease and suggest their behavior may vary with disease acuity. Their inverse trend with standard inflammatory markers resembles the behavior of negative acute-phase reactants. Further research into ceramide flux dynamics in the acute-to-subacute phase of disease is needed.

Fields of Study & Subjects

COVID-19 Clinical Research Studies Sphingolipid Metabolism and Signaling Sepsis Diagnosis and Treatment

Publication details

Journal / source
Open Forum Infectious Diseases
Volume
13
Issue
2
Pages
ofag052–ofag052
Publication date
1 February 2026
Language
EN