Pre-deployment differences in glucocorticoid sensitivity of leukocytes in soldiers developing symptoms of PTSD, depression or fatigue persist after return from military deployment

被引:20
作者
van Zuiden, Mirjam [1 ]
Kavelaars, Annemieke [2 ]
Vermetten, Eric [3 ,4 ,5 ,6 ]
Olff, Miranda [1 ,5 ]
Geuze, Elbert [3 ,4 ]
Heijnen, Cobi [2 ,7 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Psychiat, Ctr Psychotrauma, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Texas MD Anderson Canc Ctr, Dept Symptom Res, Neuroimmunol Lab, Houston, TX 77030 USA
[3] Minist Def, Res Ctr Mil Mental Hlth, Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Dept Psychiat, Brain Ctr Rudolf Magnus, Utrecht, Netherlands
[5] Arg Psychotrauma Expert Grp, Diemen, Netherlands
[6] Leiden Univ, Med Ctr, Dept Psychiat, Leiden, Netherlands
[7] Univ Med Ctr Utrecht, Lab Neuroimmunol & Dev Origins Dis NIDOD, Utrecht, Netherlands
关键词
PTSD; Depression; Fatigue; Glucocorticoid receptor; Stress; Combat; POSTTRAUMATIC-STRESS-DISORDER; SELF-RATING INVENTORY; LINEAR MIXED MODELS; PSYCHOMETRIC PROPERTIES; LONGITUDINAL DATA; MAJOR DEPRESSION; IMMUNOREGULATION; PATHOPHYSIOLOGY; RESISTANCE; VETERANS;
D O I
10.1016/j.psyneuen.2014.09.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Deployed soldiers are at risk of developing stress-related conditions, including posttraumatic stress disorder (PTSD), major depressive disorder (MDD), and severe fatigue. We previously observed condition- and cell-specific differences in sensitivity of immune cells for regulation by glucocorticoids (GCs) pre-deployment between male soldiers with and without subsequent development of high levels of these stress-related symptoms. Here we investigated whether these pre-deployment dysregulations in GC-sensitivity of immune cells persisted after return from military deployment. In a prospective, longitudinal study including 721 male and female soldiers, the in vitro GC-sensitivity of monocytes and T-cells was assessed prior to deployment and one and six months post-deployment. Differences in the longitudinal course of sensitivity for regulation by dexamethasone (DEX) of LPS-stimulated TNF-alpha production and PHA-stimulated T-cell proliferation between soldiers with and without subsequent symptom development were investigated using linear mixed models. Within the whole group, DEX-sensitivity of monocytes was significantly decreased at six months post-deployment compared to the assessments pre-deployment and one month post-deployment. The DEX-sensitivity of T-cells did not significantly change over time. Participants developing high levels of PTSD symptoms showed high DEX-sensitivity of T-cells, while participants developing high levels of depressive symptoms showed low DEX-sensitivity of T-cells before deployment that persisted at the two time points after return. In addition, participants developing severe fatigue had low DEX-sensitivity of monocytes at all assessments. Our finding that the previously observed pre-deployment group differences in peripheral GC-sensitivity persisted until at least six months after return indicates that in vitro GC-sensitivity of T-cells and monocytes may represent a persistent biological vulnerability factor for development of stress-related conditions PTSD, depression and fatigue. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:513 / 524
页数:12
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