Clinical Neurophysiology Research Laboratory, Western Psychiatric Institute & Clinic, Department of Psychiatry, University of Pittsburgh School of Medicine, United States.
Clinical Neurophysiology Research Laboratory, Western Psychiatric Institute & Clinic, Department of Psychiatry, University of Pittsburgh School of Medicine, United States.
Schizophr Res. 2018 May;195:421-427. doi: 10.1016/j.schres.2017.10.011. Epub 2017 Oct 22.
Auditory scene analysis (ASA) dysfunction is likely an important component of the symptomatology of schizophrenia. Auditory object segmentation, the grouping of sequential acoustic elements into temporally-distinct auditory objects, can be assessed with electroencephalography through measurement of the auditory segmentation potential (ASP). Further, N2 responses to the initial and final elements of auditory objects are enhanced relative to medial elements, which may indicate auditory object edge detection (initiation and termination). Both ASP and N2 modulation are impaired in long-term schizophrenia. To determine whether these deficits are present early in disease course, we compared ASP and N2 modulation between individuals at their first episode of psychosis within the schizophrenia spectrum (FE, N=20) and matched healthy controls (N=24). The ASP was reduced by >40% in FE; however, N2 modulation was not statistically different from HC. This suggests that auditory segmentation (ASP) deficits exist at this early stage of schizophrenia, but auditory edge detection (N2 modulation) is relatively intact. In a subset of subjects for whom structural MRIs were available (N=14 per group), ASP sources were localized to midcingulate cortex (MCC) and temporal auditory cortex. Neurophysiological activity in FE was reduced in MCC, an area linked to aberrant perceptual organization, negative symptoms, and cognitive dysfunction in schizophrenia, but not temporal auditory cortex. This study supports the validity of the ASP for measurement of auditory object segmentation and suggests that the ASP may be useful as an early index of schizophrenia-related MCC dysfunction. Further, ASP deficits may serve as a viable biomarker of disease presence.
听觉场景分析(ASA)功能障碍可能是精神分裂症症状的重要组成部分。听觉对象分割,即将连续的声学元素分组为时间上不同的听觉对象,可以通过测量听觉分割电位(ASP)来评估脑电图。此外,对听觉对象的初始和最终元素的 N2 反应相对于中间元素增强,这可能表明听觉对象边缘检测(启动和终止)。长期精神分裂症患者的 ASP 和 N2 调制均受损。为了确定这些缺陷是否在疾病早期出现,我们比较了精神分裂症谱系内首次精神病发作的个体(FE,N=20)和匹配的健康对照组(N=24)之间的 ASP 和 N2 调制。FE 中的 ASP 减少了>40%;但是,N2 调制与 HC 没有统计学差异。这表明听觉分割(ASP)缺陷存在于精神分裂症的早期阶段,但听觉边缘检测(N2 调制)相对完整。在有结构 MRI 可用的受试者亚组中(每组 N=14),ASP 源被定位到中扣带皮层(MCC)和颞听觉皮层。FE 中的神经生理活动在 MCC 中减少,MCC 与精神分裂症中的异常知觉组织,阴性症状和认知功能障碍有关,但与颞听觉皮层无关。这项研究支持了 ASP 用于测量听觉对象分割的有效性,并表明 ASP 可能是评估与精神分裂症相关的 MCC 功能障碍的有用指标。此外,ASP 缺陷可能是疾病存在的可行生物标志物。