PACAP a mediator of inflammation following trauma exposure and mild traumatic brain injury: Differential effects in males and females

IF 8.8 2区 医学 Q1 IMMUNOLOGY
Shane W. Adams , Aoife O’Donovan , Thomas C. Neylan , Victor May , Sayamwong E. Hammack , Kerry Ressler , Odette A. Harris , Sabra S. Inslicht
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引用次数: 0

Abstract

Individual differences in systemic responses to trauma exposure, posttraumatic stress disorder (PTSD), and/or mild traumatic brain injury (mTBI) may help account for differential risk of adverse sequalae in females and heterogeneity in pathophysiology, symptoms, and treatment responses. Accordingly, this study investigated sex differences in the association between neuroendocrine (pituitary adenylate cyclase-activating polypeptide [PACAP]) and inflammatory markers following lifespan trauma exposure, PTSD, and mTBI in 71 trauma-exposed veteran and non-veteran males (n = 41) and females (n = 30). Two mediation models were proposed and evaluated, informed by an existing theoretical model. Both mediation models examined elevated PACAP as a key variable that may be associated with elevated inflammatory cytokine interleukin-6 (IL-6). The first model evaluated this effect following psychological trauma exposure and the second following mTBI. Trauma exposure and mTBI accounted for a large proportion of sex differences in PACAP and inflammation independent of the effects of time since the events (M = 8–11 years), PTSD symptom severity and diagnostic status, suggesting potentially long-term impacts of trauma exposure and mTBI on systemic pathophysiological responses regardless of PTSD symptom variations. Specifically, PACAP mediated the relationship between cumulative trauma exposure and IL-6 as well as mTBI history and IL-6, with a stronger mediating effect of PACAP on mTBI (β = 0.352) than trauma exposure (β = 0.149). Sex differences were observed in which males with mTBI histories had significantly elevated PACAP levels (Hedges’ g = 0.79) and females with mTBI histories had significantly elevated IL-6 levels (Hedges’ g = 1.03). PACAP was uniquely associated with trauma exposure in females (β = 0.56) and mTBI in males (β = 0.35). Conversely, IL-6 was uniquely associated with mTBI in females (β = 0.47–0.61) and trauma exposure in males (β = 0.42–0.54). For both sexes, childhood emotional neglect was uniquely associated with PACAP and inflammation later in life. This study presents preliminary evidence of the association between PACAP and inflammation following both trauma exposure and mTBI, which was differentially related in males and females. Although further study is needed, findings have the potential to help explicate heterogeneous presentations and differential risk of trauma-related pathology and mTBI that could lead to more targeted and effective treatments.

Abstract Image

PACAP是创伤暴露和轻度创伤性脑损伤后炎症的介质:在男性和女性中的不同影响
对创伤暴露、创伤后应激障碍(PTSD)和/或轻度创伤性脑损伤(mTBI)的系统反应的个体差异可能有助于解释女性不良后遗症的不同风险以及病理生理、症状和治疗反应的异质性。因此,本研究调查了71名创伤暴露的退伍军人和非退伍军人(n = 41)和女性(n = 30)在终身创伤暴露、PTSD和mTBI后神经内分泌(垂体腺苷酸环化酶激活多肽[PACAP])和炎症标志物之间关系的性别差异。在现有理论模型的基础上,提出并评估了两种中介模型。两种中介模型都将PACAP升高作为可能与炎症细胞因子白介素-6 (IL-6)升高相关的关键变量。第一个模型评估了心理创伤暴露后的影响,第二个模型评估了mTBI后的影响。创伤暴露和mTBI在PACAP和炎症的性别差异中占很大比例,独立于事件发生时间(M = 8-11年)、创伤后应激障碍症状严重程度和诊断状态的影响,提示创伤暴露和mTBI对全身病理生理反应的潜在长期影响,无论PTSD症状如何变化。具体而言,PACAP介导累积创伤暴露与IL-6、mTBI史与IL-6之间的关系,其中PACAP对mTBI的介导作用(β = 0.352)强于创伤暴露(β = 0.149)。有mTBI病史的男性PACAP水平显著升高(Hedges ' g = 0.79),有mTBI病史的女性IL-6水平显著升高(Hedges ' g = 1.03)。PACAP与女性创伤暴露(β = 0.56)和男性mTBI (β = 0.35)有独特的相关性。相反,IL-6与女性mTBI (β = 0.47-0.61)和男性创伤暴露(β = 0.42-0.54)相关。无论男女,童年时期的情感忽视都与以后的PACAP和炎症有独特的联系。本研究提供了创伤暴露和mTBI后PACAP与炎症之间关联的初步证据,这在男性和女性中存在差异。虽然还需要进一步的研究,但这些发现有可能有助于解释创伤相关病理和mTBI的异质性表现和不同风险,从而导致更有针对性和更有效的治疗。
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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