Department of Psychiatry, University of California San Diego, La Jolla, CA.
Department of Psychology, Colorado State University, Fort Collins, CO.
Schizophr Bull. 2021 Mar 16;47(2):373-385. doi: 10.1093/schbul/sbaa116.
Cognitive impairment is a hallmark of schizophrenia and a robust predictor of functional outcomes. Impairments are found in all phases of the illness and are only moderately attenuated by currently approved therapeutics. Neurophysiological indices of sensory discrimination (ie, mismatch negativity (MMN) and P3a amplitudes) and gamma-band auditory steady-state response (ASSR; power and phase locking) are translational biomarkers widely used in the development of novel therapeutics for neuropsychiatric disorders. It is unclear whether laboratory-based EEG measures add explanatory power to well-established models that use only cognitive, clinical, and functional outcome measures. Moreover, it is unclear if measures of sensory discrimination and gamma-band ASSR uniquely contribute to putative causal pathways linking sensory discrimination, neurocognition, negative symptoms, and functional outcomes in schizophrenia. To answer these questions, hierarchical associations among sensory processing, neurocognition, clinical symptoms, and functional outcomes were assessed via structural equation modeling in a large sample of schizophrenia patients (n = 695) and healthy comparison subjects (n = 503). The results showed that the neurophysiologic indices of sensory discrimination and gamma-band ASSR both significantly contribute to and yield unique hierarchical, "bottom-up" effects on neurocognition, symptoms, and functioning. Measures of sensory discrimination showed direct effects on neurocognition and negative symptoms, while gamma-band ASSR had a direct effect on neurocognition in patients. Continued investigation of the neural mechanisms underlying abnormal networks of MMN/P3a and gamma-band ASSR is needed to clarify the pathophysiology of schizophrenia and the development of novel therapeutic interventions.
认知障碍是精神分裂症的一个标志,也是功能结果的一个强有力的预测指标。在疾病的所有阶段都发现了认知障碍,而且目前批准的治疗方法只能适度减轻这些障碍。感觉辨别(即失匹配负波 (MMN) 和 P3a 幅度)和γ波段听觉稳态反应 (ASSR;功率和相位锁定)的神经生理指标是广泛用于神经精神疾病新型治疗方法开发的转化生物标志物。目前还不清楚基于实验室的脑电图测量是否会为仅使用认知、临床和功能结果测量的成熟模型增加解释力。此外,尚不清楚感觉辨别和γ波段 ASSR 测量是否可以独特地为精神分裂症中感觉辨别、神经认知、阴性症状和功能结果之间的假定因果途径做出贡献。为了回答这些问题,通过结构方程模型在大量精神分裂症患者(n = 695)和健康对照受试者(n = 503)中评估了感觉处理、神经认知、临床症状和功能结果之间的层次关联。结果表明,感觉辨别和γ波段 ASSR 的神经生理指标都对神经认知、症状和功能产生了显著的、独特的、自下而上的影响。感觉辨别测量对神经认知和阴性症状有直接影响,而 γ 波段 ASSR 对患者的神经认知有直接影响。需要进一步研究 MMN/P3a 和 γ 波段 ASSR 异常网络的神经机制,以阐明精神分裂症的病理生理学和新型治疗干预措施的发展。