Intensive care medicine experimental · 2025
Unravelling the complex inflammatory landscape of COVID-19 infection: a pathway to biomarkers identification in infection-associated delirium in the ICU.
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Born Tristan, Perreau Matthieu, Axisa Pierre-Paul, Fenwick Craig, Pinto Andrea, Ben-Hamouda Nawfel, Rossetti Andrea O, Du Pasquier Renaud, Chiche Jean-Daniel, Bernard-Valnet Raphaël
Аннотация
BACKGROUND: Delirium is a serious complication in patients with COVID-19-related acute respiratory distress syndrome (ARDS) admitted to the intensive care unit (ICU). Although numerous clinical risk factors have been identified, the immunologic pathways underlying delirium remain unclear. In this retrospective cohort study, we investigated high-dimensional immune signatures in ICU patients to delineate peripheral immune markers associated with delirium. We also explored machine learning (ML) approaches to enhance biomarker discovery and strengthen predictive modelling through synthetic data generation.
METHODS: We studied a cohort of 62 COVID-19 ARDS patients admitted to the ICU at Lausanne University Hospital, Switzerland. The primary analysis compared patients within this cohort who developed delirium (n = 39) to those who remained delirium-free (n = 23). As a baseline for disease severity, we also compared the ICU cohort to 55 non-ICU COVID-19 patients and 450 healthy individuals. We performed high-dimensional immunophenotyping of cytokines, chemokines, and growth factors using multiplex beads assay, along with immune cell profiling via mass cytometry (CyTOF). Ridge regression has been employed to build classification models. We also generated synthetic samples using beta-variational autoencoders to improve sample size and subsequently model stability.
RESULTS: Delirious patients exhibited a distinctive immune signature, including elevated CXCL1, CCL11, CXCL13, HGF, and VEGF-A, coupled with reduced IL-1α, IL-21, and IL-22. Alterations in immune cell populations featured increased exhausted B cells and decreases in CXCR3 + CD4 + T cells, IgM + unswitched memory B cells, and HLA-DR + activated T cells. Leveraging these high-dimensional data, we trained ridge regression models to predict delirium. Incorporating synthetic data helped stabilize the models with a best-performing model achieving an area under the curve (AUC) of 0.95, with high sensitivity (93%) and specificity (86%), based on 12 identified markers.
CONCLUSION: Our findings demonstrate a distinct immune profile linked to ICU delirium and illustrate how ML can enhance biomarker discovery. Further prospective validation may refine these markers and guide precision-targeted interventions for mitigating delirium in critically ill populations.
METHODS: We studied a cohort of 62 COVID-19 ARDS patients admitted to the ICU at Lausanne University Hospital, Switzerland. The primary analysis compared patients within this cohort who developed delirium (n = 39) to those who remained delirium-free (n = 23). As a baseline for disease severity, we also compared the ICU cohort to 55 non-ICU COVID-19 patients and 450 healthy individuals. We performed high-dimensional immunophenotyping of cytokines, chemokines, and growth factors using multiplex beads assay, along with immune cell profiling via mass cytometry (CyTOF). Ridge regression has been employed to build classification models. We also generated synthetic samples using beta-variational autoencoders to improve sample size and subsequently model stability.
RESULTS: Delirious patients exhibited a distinctive immune signature, including elevated CXCL1, CCL11, CXCL13, HGF, and VEGF-A, coupled with reduced IL-1α, IL-21, and IL-22. Alterations in immune cell populations featured increased exhausted B cells and decreases in CXCR3 + CD4 + T cells, IgM + unswitched memory B cells, and HLA-DR + activated T cells. Leveraging these high-dimensional data, we trained ridge regression models to predict delirium. Incorporating synthetic data helped stabilize the models with a best-performing model achieving an area under the curve (AUC) of 0.95, with high sensitivity (93%) and specificity (86%), based on 12 identified markers.
CONCLUSION: Our findings demonstrate a distinct immune profile linked to ICU delirium and illustrate how ML can enhance biomarker discovery. Further prospective validation may refine these markers and guide precision-targeted interventions for mitigating delirium in critically ill populations.