Woźny-Rasała Izabela, Ogłodek Ewa Alicja
Collegium Medicum, Jan Dlugosz University in Częstochowa, Waszyngtona 4/8 Street, 42-200 Częstochowa, Poland.
Int J Mol Sci. 2025 Aug 3;26(15):7506. doi: 10.3390/ijms26157506.
Post-traumatic stress disorder (PTSD) is a chronic mental health condition resulting from exposure to traumatic events. It is associated with long-term neurobiological changes and disturbances in emotional regulation. Understanding the sociodemographic profiles, biomarkers, and emotional control in patients with PTSD helps to better comprehend the impact of the disorder on the body and its clinical course. An analysis of biomarkers such as Interleukin-18 (IL-18), Inositol-Requiring Enzyme 1 (IRE1), Phosphorylated Extracellular Signal-Regulated Kinase (pERK), and Activating Transcription Factor-6 (ATF-6) in PTSD patients with varying durations of illness (≤5 years and >5 years) and a control group without PTSD revealed significant differences. Patients with recently diagnosed PTSD (≤5 years) showed markedly elevated levels of inflammatory and cellular stress markers, indicating an intense neuroinflammatory response during the acute phase of the disorder. In the chronic PTSD group (>5 years), the levels of these biomarkers were lower than in the recently diagnosed group, but still significantly higher than in the control group. An opposite trend was observed regarding the suppression of negative emotions, as measured by the Courtauld Emotional Control Scale (CECS): individuals with chronic PTSD exhibited a significantly greater suppression of anger, depression, and anxiety than those with recent PTSD or healthy controls. Correlations between biomarkers were strongest in individuals with chronic PTSD, suggesting a persistent neuroinflammatory dysfunction. However, the relationships between biomarkers and emotional suppression varied depending on the stage of PTSD. These findings highlight the critical role of PTSD duration in shaping the neurobiological and emotional mechanisms of the disorder, which may have important implications for therapeutic strategies and patient monitoring.
创伤后应激障碍(PTSD)是一种因暴露于创伤性事件而导致的慢性心理健康状况。它与长期的神经生物学变化以及情绪调节紊乱有关。了解PTSD患者的社会人口统计学特征、生物标志物和情绪控制,有助于更好地理解该疾病对身体的影响及其临床病程。对不同病程(≤5年和>5年)的PTSD患者以及无PTSD的对照组中的白细胞介素-18(IL-18)、肌醇需求酶1(IRE1)、磷酸化细胞外信号调节激酶(pERK)和激活转录因子6(ATF-6)等生物标志物进行分析,结果显示存在显著差异。近期诊断为PTSD(≤5年)的患者炎症和细胞应激标志物水平明显升高,表明在该疾病急性期存在强烈的神经炎症反应。在慢性PTSD组(>5年)中,这些生物标志物的水平低于近期诊断组,但仍显著高于对照组。通过考陶尔德情绪控制量表(CECS)测量发现,在抑制负面情绪方面观察到相反的趋势:慢性PTSD患者比近期PTSD患者或健康对照组在抑制愤怒、抑郁和焦虑方面表现出明显更强的能力。生物标志物之间的相关性在慢性PTSD患者中最强,表明存在持续的神经炎症功能障碍。然而,生物标志物与情绪抑制之间的关系因PTSD阶段而异。这些发现突出了PTSD病程在塑造该疾病神经生物学和情绪机制方面的关键作用,这可能对治疗策略和患者监测具有重要意义。