Carol Emily E, Spencer Robert L, Mittal Vijay A
Laboratory for Early Psychosis (LEAP) Center, Psychotic Disorders Division, McLean Hospital and Harvard Medical School, Belmont, MA, United States.
Spener Neuroendocrinology Laboratory, Department of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO, United States.
Front Psychiatry. 2021 Feb 19;12:641762. doi: 10.3389/fpsyt.2021.641762. eCollection 2021.
Deficits in stress-response systems are a characteristic of schizophrenia and psychosis spectrum illnesses, and recent evidence suggests that this impairment may be evident in those at clinical high-risk (CHR) for the development of a psychotic disorder. However, there is limited research specifically investigating biological and subjective stress reactivity in CHR individuals. In the present study, 38 CHR individuals and group of 38 control individuals participated in the Trier Social Stress Test (TSST), an experimentally induced psychosocial stressor. Changes in salivary cortisol and alpha amylase, as well as self-reported units of distress (SUDS), were evaluated. Interestingly, the TSST did not induce a change in cortisol levels in either group, though the CHR group did show higher overall cortisol levels throughout the TSST (pre-anticipation period through recovery period). However, indicative of an effective task manipulation, the TSST did illicit an increase in alpha amylase in both groups. CHR participants exhibited higher levels of subjective stress prior to the stressor compared to the control group and CHR SUDs did not significantly increase in response to the stressor. In contrast, the control group showed an increase in SUDS in response to the stressor. Notably, SUDS for the control group post task mirrored the levels CHR youth endorsed prior to the stressor. Taken together, these findings suggest that there may be a functional relationship between persistently elevated cortisol and chronic high levels of subjective distress in CHR individuals.
应激反应系统的缺陷是精神分裂症和精神病谱系疾病的一个特征,最近的证据表明,这种损害在临床高危(CHR)的精神病性障碍患者中可能很明显。然而,专门研究CHR个体的生物学和主观应激反应性的研究有限。在本研究中,38名CHR个体和38名对照个体参与了特里尔社会应激测试(TSST),这是一种实验诱导的心理社会应激源。评估了唾液皮质醇和α淀粉酶的变化以及自我报告的痛苦单位(SUDS)。有趣的是,TSST在两组中均未引起皮质醇水平的变化,尽管CHR组在整个TSST过程中(预期前期至恢复期)确实显示出总体皮质醇水平较高。然而,作为有效任务操作的指标,TSST确实使两组中的α淀粉酶均增加。与对照组相比,CHR参与者在应激源之前表现出更高水平的主观应激,并且CHR的SUDS并未因应激源而显著增加。相比之下,对照组的SUDS因应激源而增加。值得注意的是,任务后对照组的SUDS水平与CHR青年在应激源之前认可的水平相当。综上所述,这些发现表明,CHR个体中持续升高的皮质醇与慢性高水平的主观痛苦之间可能存在功能关系。