Jiang Xinyu, Gou Mengzhuang, Yin Yi, Chen Wenjin, Li Yanli, Chen Song, Pan Shujuan, Luo Xingguang, Tan Shuping, Tian Baopeng, Li Wei, Tong Jinghui, Wang Jue, Li Hongna, Yu Ting, Wang Zhiren, Zhang Ping, Huang Junchao, Tian Li, Kochunov Peter, Li Chiang-Shan R, Hong L Elliot, Tan Yunlong
Peking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing, China.
Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Psychoneuroendocrinology. 2025 Sep;179:107501. doi: 10.1016/j.psyneuen.2025.107501. Epub 2025 Jun 3.
Stress plays a critical role in schizophrenia pathogenesis, and blunted cortisol responses to acute stress exposure among patients with schizophrenia may be related to damaged white matter (WM) fibers in specific brain regions. The present aim was to assess correlations between cortisol response patterns and changes in WM integrity in patients with schizophrenia and to determine if such changes relate to the duration of illness. This study included patients with chronic schizophrenia (PCS, n = 92), patients with first-episode schizophrenia (PFS, n = 86), and healthy controls (HC, n = 77). All participants were subjected to the Paced Auditory Serial Addition Task and the Mirror Tracing Persistence Task. Saliva samples were collected 0 min before tasks, 20 and 40 min after task completion. Cortisol levels were assessed using highly sensitive liquid chromatography and tandem mass spectrometry. We used diffusion tensor imaging (DTI) to assess WM microstructural integrity. Clinical psychopathology was assessed using the Positive and Negative Syndrome Scale. The repeated measures analysis of variance and pairwise comparisons demonstrated distinct cortisol response patterns across groups. In the HC group, cortisol levels peaked before tasks, declining rapidly thereafter. In the PFS group, cortisol levels significantly increased 20 min post-exposure, with no significant decrease observed at the final 40-minutes time point. In the PCS group, cortisol levels remained relatively high, with no significant fluctuations over time. Furthermore, WM integrity progressively deteriorated as disease duration increased. A negative correlation was observed between WM tract integrity and prolonged cortisol reactivity in the PFS group, whereas this correlation was positive in the HC group and absent in the PCS group. Changes in salivary cortisol levels did not correlate with clinical symptoms in our patients with schizophrenia. These findings suggest that stress has the potential to contribute to schizophrenia by exacerbating WM damage. Stress-induced cortisol response patterns, which vary according to disease duration, may represent a potential biomarker of schizophrenia.
应激在精神分裂症发病机制中起关键作用,精神分裂症患者对急性应激暴露的皮质醇反应迟钝可能与特定脑区白质(WM)纤维受损有关。本研究的目的是评估精神分裂症患者皮质醇反应模式与WM完整性变化之间的相关性,并确定这些变化是否与病程有关。本研究纳入了慢性精神分裂症患者(PCS,n = 92)、首发精神分裂症患者(PFS,n = 86)和健康对照者(HC,n = 77)。所有参与者均接受了听觉连续加法任务和镜像追踪持续任务。在任务前0分钟、任务完成后20分钟和40分钟收集唾液样本。使用高灵敏度液相色谱和串联质谱法评估皮质醇水平。我们使用扩散张量成像(DTI)评估WM微观结构完整性。使用阳性和阴性症状量表评估临床精神病理学。重复测量方差分析和两两比较显示各组皮质醇反应模式不同。在HC组中,皮质醇水平在任务前达到峰值,随后迅速下降。在PFS组中,暴露后20分钟皮质醇水平显著升高,在最后40分钟时间点未观察到显著下降。在PCS组中,皮质醇水平保持相对较高,随时间无显著波动。此外,随着病程延长,WM完整性逐渐恶化。在PFS组中,WM束完整性与皮质醇反应性延长呈负相关,而在HC组中这种相关性为正,在PCS组中不存在。我们的精神分裂症患者唾液皮质醇水平变化与临床症状无关。这些发现表明,应激可能通过加剧WM损伤而导致精神分裂症。应激诱导的皮质醇反应模式因病程而异,可能代表精神分裂症的潜在生物标志物。