PTSD and suPAR: A multicohort investigation of chronic inflammation.

Abstract

Posttraumatic stress disorder (PTSD) is associated with poor health. Prior research has shown stressful events are associated with inflammatory biomarkers, such as soluble urokinase plasminogen activator receptor (suPAR), suggesting systemic chronic inflammation could be a mechanism linking adversity to poor health. In this study, we examined associations of PTSD and suPAR in two research cohorts-the E-Risk Study (United Kingdom; n = 1,389) and the Dunedin Multidisciplinary Health and Development Study (New Zealand; n = 927)-and a clinical cohort of medical patients (Denmark; n = 29,285). We also present results from two commonly assessed inflammatory biomarkers: C-reactive protein (CRP) and interleukin-6 (IL-6). People with a lifetime history of PTSD had higher suPAR at age 18 in E-Risk (β = 0.21, p = 0.046) and age 38 in the Dunedin Study (β = 0.23, p = 0.025), but not age 45 in the Dunedin Study (β = 0.18, p = 0.050). Individuals who developed PTSD in the year prior to age 45 in Dunedin had significant increases in suPAR from age 38 to 45 (β = 0.45, p = 0.034). Danish patients with a recent diagnosis of PTSD or a stress-related psychiatric disorder had higher levels of suPAR compared to propensity score-matched patients without such diagnoses (0.10 < βs < 0.24, ps < 0.05). CRP and IL-6 did not show consistent associations with PTSD. These results suggest that PTSD is associated with suPAR and that systemic chronic inflammation could help explain how trauma and PTSD might result in poor health.

Department

Description

Provenance

Subjects

CRP, IL-6, Inflammation, PTSD, Trauma, suPAR

Citation

Published Version (Please cite this version)

10.1016/j.bbi.2025.106159

Publication Info

Bourassa, Kyle J, Terrie E Moffitt, Louise Arseneault, Ashleigh Barrett-Young, Andrea Danese, Melanie E Garrett, Renate Houts, Timothy Matthews, et al. (2025). PTSD and suPAR: A multicohort investigation of chronic inflammation. Brain, behavior, and immunity, 131. p. 106159. 10.1016/j.bbi.2025.106159 Retrieved from https://hdl.handle.net/10161/33574.

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Scholars@Duke

Bourassa

Kyle Bourassa

Affiliate

Kyle Bourassa is a Staff Psychologist in the Research Service of the Durham VA Medical System, a Snior Research Fellow and Affiliate Faculty at Georgetown University in the Department of Psychology, and a Senior Fellow of the Center for the Study of Aging and Human Development at Duke University Medical Center

Beckham

Jean Crowell Beckham

Professor in Psychiatry and Behavioral Sciences

Interest in assessment and treatment of trauma, particularly as occurs for both women and men during military service; focus in treatment outcome of differential and collective contribution for psychopharmacological and behavioral interventions in PTSD populations; long term physical health effects of chronic posttraumatic stress disorder.

Ashley-Koch

Allison Elizabeth Ashley-Koch

Professor in Medicine

My work focuses on the dissection of human traits using multi-omic technologies (genetics, epigenetics, metabolomics and proteomics).  I am investigating the basis of several neurological and psychiatric conditions such as neural tube defects and post-traumatic stress disorder. I also study modifiers of sickle cell disease.

Kimbrel

Nathan Andrew Kimbrel

Associate Professor of Psychiatry and Behavioral Sciences

My primary areas of interest include the etiology, assessment, and treatment of PTSD, depression, suicide, and non-suicidal self-injury. I primarily work with veterans, firefighters, and emergency medical personnel due to their high levels of occupational exposure to traumatic stress. I also have long-standing interests in genetics, epigenetics, GxE research, personality, smoking, comorbidity, and statistical modeling procedures, such as CFA, SEM, and mixture modeling.

Caspi

Avshalom Caspi

Edward M. Arnett Distinguished Professor of Psychology and Neuroscience

Caspi’s research is concerned with three questions: (1) How do childhood experiences shape aging and the course of health inequalities across the life span?  (2) How do genetic differences between people shape the way they respond to their environments? (3) How do mental health problems unfold across and shape the life course? 


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