Proinflammatory milieu in combat-related PTSD is independent of depression and early life stress

• Published in: Brain, behavior, and immunity Vol. 42; no. Jun 12; pp. 81 - 88
• Main Authors: Lindqvist, Daniel, Wolkowitz, Owen M, Mellon, Synthia, Yehuda, Rachel, Flory, Janine D, Henn-Haase, Clare, Bierer, Linda M, Abu-Amara, Duna, Coy, Michelle, Neylan, Thomas C, Makotkine, Iouri, Reus, Victor I, Yan, Xiaodan, Taylor, Nicole M, Marmar, Charles R, Dhabhar, Firdaus S
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.11.2014
• Subjects: Adult; Allergy and Immunology; C-Reactive Protein - metabolism; Clinical Medicine; Combat; Combat Disorders - blood; Combat Disorders - complications; Cytokines; Cytokines - blood; Depression; Depressive Disorder - blood; Depressive Disorder - complications; Early life trauma; Humans; Inflammation; Inflammation - blood; Inflammation - complications; Interleukin-1beta - blood; Interleukin-6 - blood; Klinisk medicin; Life Change Events; Male; Medical and Health Sciences; Medicin och hälsovetenskap; Military Personnel; Neurologi; Neurology; Post-traumatic stress disorder (PTSD); Psychiatry; Stress Disorders, Post-Traumatic - blood; Stress Disorders, Post-Traumatic - complications; Stress, Psychological - blood; Stress, Psychological - complications; Tumor Necrosis Factor-alpha - blood; Young Adult; Depression; Inflammation; Cytokines; Post-traumatic stress disorder (PTSD); Early life trauma; Combat
• ISSN: 0889-1591; 1090-2139; 1090-2139
• DOI: 10.1016/j.bbi.2014.06.003

Abstract Background Chronic inflammation may be involved in combat-related post-traumatic stress disorder (PTSD) and may help explain comorbid physical diseases. However, the extent to which combat exposure per se , depression, or early life trauma, all of which are associated with combat PTSD, may confound the relationship between PTSD and inflammation is unclear. Methods We quantified interleukin (IL)-6, IL-1β, tumor necrosis factor (TNF)-α, interferon (IFN)-γ, and C-reactive protein (CRP) in 51 combat-exposed males with PTSD and 51 combat-exposed males without PTSD, and assessed PTSD and depression severity as well as history of early life trauma. To decrease the possibility of Type I errors, we summed standardized scores of IL-1β, IL-6, TNFα, IFNγ and CRP into a total “pro-inflammatory score”. PTSD symptom severity was assessed with the Clinician Administered PTSD Scale (CAPS) rating scale. Results Subjects with PTSD had significantly higher pro-inflammatory scores compared to combat-exposed subjects without PTSD ( p = 0.006), and even after controlling for early life trauma, depression diagnosis and severity, body mass index, ethnicity, education, asthma/allergies, time since combat and the use of possibly confounding medications ( p = 0.002). Within the PTSD group, the pro-inflammatory score was not significantly correlated with depressive symptom severity, CAPS total score, or with the number of early life traumas. Conclusions Combat-related PTSD in males is associated with higher levels of pro-inflammatory cytokines, even after accounting for depression and early life trauma. These results, from one of the largest studies of inflammatory cytokines in PTSD to date, suggest that immune activation may be a core element of PTSD pathophysiology more so than a signature of combat exposure alone.