Mental Illness Research, Education and Clinical Center, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, USA.
Psychol Med. 2012 Jan;42(1):85-97. doi: 10.1017/S0033291711001061. Epub 2011 Jul 11.
Deficits in automatic sensory discrimination, as indexed by a reduction in the mismatch negativity (MMN) and P3a event-related potential amplitudes, are well documented in chronic schizophrenia. However, MMN and P3a have not been sufficiently studied early in the course of psychotic illness. The present study aimed to investigate MMN, P3a and reorienting negativity (RON) across the course of schizophrenia.
MMN, P3a, and RON were assessed in 118 subjects across four groups: (1) individuals at risk for psychosis (n=26); (2) recent-onset patients (n=31); (3) chronic patients (n=33); and (4) normal controls (n=28) using a duration-deviant auditory oddball paradigm.
Frontocentral deficits in MMN and P3a were present in all patient groups. The at-risk group's MMN and P3a amplitudes were intermediate to those of the control and recent-onset groups. The recent-onset and chronic patients, but not the at-risk subjects, showed significant RON amplitude reductions, relative to the control group. Associations between MMN, P3a, RON and psychosocial functioning were present in the chronic patients. In the at-risk subjects, P3a and RON deficits were significantly associated with higher levels of negative symptoms.
Abnormalities in the automatic processes of sensory discrimination, orienting and reorienting of attention are evident in the early phases of schizophrenia and raise the possibility of progressive worsening across stages of the illness. The finding that MMN and P3a, but not RON, were reduced before psychosis onset supports the continued examination of these components as potential early biomarkers of schizophrenia.
慢性精神分裂症患者的自动感觉辨别缺陷,表现为失匹配负波(MMN)和 P3a 事件相关电位幅度降低,已有充分的文献记载。然而,在精神病早期,MMN 和 P3a 并没有得到充分的研究。本研究旨在探讨精神分裂症发病过程中的 MMN、P3a 和重新定向负波(RON)。
使用时长偏离听觉Oddball 范式,对 118 名受试者(4 组)的 MMN、P3a 和重新定向负波进行了评估:(1)有精神病风险的个体(n=26);(2)近期发病的患者(n=31);(3)慢性患者(n=33);(4)正常对照组(n=28)。
所有患者组的额中央区 MMN 和 P3a 均存在缺陷。高危组的 MMN 和 P3a 振幅介于对照组和近期发病组之间。近期发病和慢性患者,而非高危组,与对照组相比,RON 振幅明显降低。在慢性患者中,MMN、P3a 和 RON 与社会心理功能之间存在相关性。在高危受试者中,P3a 和 RON 缺陷与更高水平的阴性症状显著相关。
在精神分裂症的早期阶段,自动感觉辨别、定向和重新定向注意的异常就很明显,这表明疾病的各个阶段都可能出现病情恶化。在精神病发作前,MMN 和 P3a 而不是 RON 减少的发现支持了继续检查这些成分作为精神分裂症潜在早期生物标志物的可能性。