Lee Cynthia H, Sinclair Duncan, O'Donnell Maryanne, Galletly Cherrie, Liu Dennis, Weickert Cynthia Shannon, Weickert Thomas W
School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia; Schizophrenia Research Laboratory, Neuroscience Research Australia, Randwick, NSW 2031, Australia.
University of Tasmania, Hobart, Australia.
Schizophr Res. 2019 Nov;213:87-95. doi: 10.1016/j.schres.2019.06.026. Epub 2019 Jul 8.
Altered levels of stress-signalling transcripts have been identified in post-mortem brains of people with schizophrenia, and since stress effects may be expressed throughout the body, there should be similar changes in peripheral cells. However, the extent to which these markers are altered in peripheral white blood cells of people with schizophrenia is not known. Furthermore, how peripheral cortisol and stress-related mRNA are associated with negative symptom severity and emotional states in people with schizophrenia versus schizoaffective disorder has not been determined. Whole blood samples were collected from 86 patients with either schizophrenia or schizoaffective disorder (56 people with schizophrenia and 30 people with schizoaffective disorder), and 77 healthy controls. Total RNA was isolated, cDNA was synthesized, and stress-signalling mRNA levels (for NR3C1, FKBP5, FKBP4, PTGES3 and BAG1) were determined. Stress and symptom severity scores were measured by the Depression, Anxiety and Stress Scale, and the Positive and Negative Syndrome Scale, respectively. We found increased FKBP5 mRNA, Z(156) = 2.5, p = 0.01, decreased FKBP4 mRNA, t(155) = 3.5, p ≤ 0.001, and decreased PTGES3 mRNA, t(153) = 3.0, p ≤ 0.01, in schizophrenia and schizoaffective disorder cohorts combined compared to healthy controls. Stress-related peripheral mRNA levels were differentially correlated with negative emotional states and symptom severity in schizoaffective disorder (β's = -0.45-0.56, p's = 0.05-0.001) and schizophrenia (β's = -0.34-0.38, p's = 0.04-0.03), respectively. Therefore, molecules of the stress-signalling pathway appear to differentially contribute to clinical features of schizophrenia versus schizoaffective disorder.
在精神分裂症患者的尸检大脑中已发现应激信号转录本水平发生改变,而且由于应激效应可能在全身表现出来,外周细胞中应该也有类似变化。然而,精神分裂症患者外周白细胞中这些标志物的改变程度尚不清楚。此外,与精神分裂情感障碍患者相比,精神分裂症患者外周皮质醇和应激相关mRNA如何与阴性症状严重程度及情绪状态相关联尚未确定。从86例精神分裂症或精神分裂情感障碍患者(56例精神分裂症患者和30例精神分裂情感障碍患者)以及77名健康对照者中采集全血样本。分离总RNA,合成cDNA,并测定应激信号mRNA水平(针对NR3C1、FKBP5、FKBP4、PTGES3和BAG1)。分别通过抑郁、焦虑和压力量表以及阳性和阴性症状量表测量应激和症状严重程度评分。我们发现,与健康对照者相比,精神分裂症和精神分裂情感障碍队列合并组中FKBP5 mRNA增加,Z(156) = 2.5,p = 0.01;FKBP4 mRNA减少,t(155) = 3.5,p≤0.001;PTGES3 mRNA减少,t(153) = 3.0,p≤0.01。应激相关外周mRNA水平在精神分裂情感障碍(β值 = -0.45 - 0.56,p值 = 0.05 - 0.001)和精神分裂症(β值 = -0.34 - 0.38,p值 = 0.04 - 0.03)中分别与负面情绪状态和症状严重程度存在差异相关性。因此,应激信号通路的分子似乎对精神分裂症与精神分裂情感障碍的临床特征有不同的影响。