Cellular microRNAs correlate with clinical parameters in multiple injury patients. Issue 4 (7th October 2022)

• Record Type: Journal Article
• Authors: Vicente, Diego A.; Schobel, Seth A.; Anfossi, Simone; Hensman, Hannah; Lisboa, Felipe; Robertson, Henry; Khatri, Vivek; Bradley, Matthew J.; Shimizu, Masayoshi; Buchman, Timothy G.; Davis, Thomas A.; Dente, Christopher J.; Kirk, Allan D.; Calin, George A.; Elster, Eric A.
• Is Part Of: Journal of trauma and acute care surgery. Volume 93:Issue 4(2022)
• Page Start: 427
• Page End: 438
• Publication Date: 2022-10-07
• Subjects: Trauma -- microRNA -- complications -- inflammation -- recovery; Surgical intensive care -- Periodicals; Surgical emergencies -- Periodicals; Wounds and injuries -- Surgery -- Periodicals; 617.026
• DOI: 10.1097/TA.0000000000003708
• Languages: English
• ISSNs: 2163-0755

Abstract

Abstract : In a large multicenter prospectively collected database, the Surgical Critical Care Initiative's microRNA team characterize novel changes in microRNA expression in response to severe trauma. Systemic levels of microRNAs were associated with recovery complications. #microRNA Abstract : INTRODUCTION: The pathophysiology of the inflammatory response after major trauma is complex, and the magnitude correlates with severity of tissue injury and outcomes. Study of infection-mediated immune pathways has demonstrated that cellular microRNAs may modulate the inflammatory response. The authors hypothesize that the expression of microRNAs would correlate to complicated recoveries in polytrauma patients (PtPs). METHODS: Polytrauma patients enrolled in the prospective observational Tissue and Data Acquisition Protocol with Injury Severity Score of >15 were selected for this study. Polytrauma patients were divided into complicated recoveries and uncomplicated recovery groups. Polytrauma patients' blood samples were obtained at the time of admission (T0). Established biomarkers of systemic inflammation, including cytokines and chemokines, were measured using multiplexed Luminex-based methods, and novel microRNAs were measured in plasma samples using multiplex RNA hybridization. RESULTS: Polytrauma patients (n = 180) had high Injury Severity Score (26 [20–34]) and complicated recovery rate of 33%. MicroRNAs were lower in PtPs at T0 compared with healthy controls, and bivariate analysis demonstrated that variations of microRNAs correlated with age, race, comorbidities, venous thromboembolism, pulmonary complications, complicated recovery, and mortality. Positive correlations were noted between microRNAs and interleukin 10, vascular endothelial growth factor, Acute Physiology and Chronic Health Evaluation, and Sequential Organ Failure Assessment scores. Multivariable Lasso regression analysis of predictors of complicated recovery based on microRNAs, cytokines, and chemokines revealed that miR-21-3p and monocyte chemoattractant protein-1 were predictive of complicated recovery with an area under the curve of 0.78. CONCLUSION: Systemic microRNAs were associated with poor outcomes in PtPs, and results are consistent with previously described trends in critically ill patients. These early biomarkers of inflammation might provide predictive utility in early complicated recovery diagnosis and prognosis. Because of their potential to regulate immune responses, microRNAs may provide therapeutic targets for immunomodulation. LEVEL OF EVIDENCE: Diagnostic Tests/Criteria; Level II. Abstract :