Institute of Health and Biomedical Innovation (IHBI) and School of Biomedical Sciences, 60 Musk Avenue, Queensland University of Technology, Kelvin Grove, Queensland, 4059, Australia; Gallipoli Medical Research Institute, Greenslopes Private Hospital, Newdegate Street, Greenslopes, Queensland, 4120, Australia.
Institute of Health and Biomedical Innovation (IHBI) and School of Biomedical Sciences, 60 Musk Avenue, Queensland University of Technology, Kelvin Grove, Queensland, 4059, Australia.
Compr Psychiatry. 2017 Apr;74:125-133. doi: 10.1016/j.comppsych.2017.01.015. Epub 2017 Jan 24.
Posttraumatic stress disorder (PTSD) is associated with increased inflammation and comorbid medical conditions. However, study findings for individual inflammatory marker levels have been inconsistent. Some research suggests that resilience may play a role in decreased inflammation. A polymorphism in the promoter region of the tumor necrosis factor α gene (TNFα), TNFA -308 (rs1800629) is associated with psychiatric illness but its role in PTSD is yet to be elucidated.
This study investigates a key inflammatory marker, TNFα, for its role in PTSD severity.
In a cohort of trauma-exposed Vietnam War veterans (n=299; 159 cases, 140 controls) TNF α serum levels and TNFα polymorphism rs1800629 were correlated with PTSD severity and resilience scores.
The polymorphism was associated with PTSD severity (p=0.045). There were significant group differences between cases and controls with regards to serum TNFα levels (p=0.036). Significant correlations were found between PTSD severity and elevated TNFα levels (r=0.153; p=0.009), and between resilience and decreased TNFα levels at a trend level (p=0.08) across the entire cohort. These relationships were non-significant after controlling for covariates. In the PTSD diagnostic group, a correlation of TNFα and PTSD severity was observed on a trend level (p=0.06), the relationship between TNFα and resilience remained non-significant.
To our knowledge, this is the first time rs1800629 has been investigated in PTSD contributing to a growing body of literature that identifies the GG as a risk genotype for psychiatric disorders in Caucasian cohorts. However, more research is needed to replicate our results in larger, equally well-characterized cohorts. The relationship between serum TNFα levels and PTSD severity and resilience requires further investigation.
创伤后应激障碍(PTSD)与炎症增加和合并医疗状况有关。然而,对于个别炎症标志物水平的研究结果并不一致。一些研究表明,适应力可能在降低炎症方面发挥作用。肿瘤坏死因子α基因(TNFα)启动子区域的一个多态性,TNFα-308(rs1800629)与精神疾病有关,但它在 PTSD 中的作用尚未阐明。
本研究调查了一个关键的炎症标志物 TNFα 在 PTSD 严重程度中的作用。
在一组创伤后暴露于越南战争的退伍军人队列中(n=299;159 例病例,140 例对照),TNFα 血清水平和 TNFα 多态性 rs1800629 与 PTSD 严重程度和适应力评分相关。
该多态性与 PTSD 严重程度相关(p=0.045)。病例组和对照组之间在血清 TNFα 水平方面存在显著差异(p=0.036)。在整个队列中,PTSD 严重程度与 TNFα 水平升高之间存在显著相关性(r=0.153;p=0.009),而在趋势水平上,适应力与 TNFα 水平降低之间存在相关性(p=0.08)。在控制了协变量后,这些相关性不再显著。在 PTSD 诊断组中,TNFα 与 PTSD 严重程度之间存在趋势水平上的相关性(p=0.06),而 TNFα 与适应力之间的相关性仍不显著。
据我们所知,这是首次在 PTSD 中研究 rs1800629,这为越来越多的文献提供了证据,这些文献表明 GG 是白人群体中精神疾病的风险基因型。然而,需要更多的研究来在更大、特征更相似的队列中复制我们的结果。血清 TNFα 水平与 PTSD 严重程度和适应力之间的关系需要进一步研究。