Schizophrenia Research Division, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY 10962, United States; Division of Experimental Therapeutics, Department of Psychiatry, Columbia University, New York, NY 10032, United States.
Schizophrenia Research Division, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY 10962, United States; Division of Experimental Therapeutics, Department of Psychiatry, Columbia University, New York, NY 10032, United States.
Schizophr Res. 2018 Jan;191:10-17. doi: 10.1016/j.schres.2017.07.032. Epub 2017 Aug 2.
Deficits in mismatch negativity (MMN) generation are among the best replicated neurophysiological deficits in schizophrenia, with reduced amplitude reflecting impaired information processing at the level of supratemporal auditory cortex. Differential patterns of MMN dysfunction according to deviant types have been reported across studies, with some research groups showing impairment in duration MMN but not frequency MMN, and other research groups reporting both findings. We evaluate the hypothesis that recruitment setting, reflecting current functional status, might be an important determinant of the pattern of MMN dysfunction. Here, we evaluated patterns of MMN dysfunction, along with tone matching and neuropsychological performance in subjects drawn from 1) a predominant inpatient/residential care setting (Nathan Kline Institute) and 2) a predominant outpatient setting (Columbia University). As predicted, compared to healthy controls, deficits in duration MMN were observed across sites, whereas deficits in frequency MMN/tone matching were confined to the chronic inpatient setting. Within patients, the frequency MMN deficit was highly correlated with impairments in tone matching ability across sites (r=-0.52, p<0.0001), as well as impairments in verbal learning (r=-0.54, p<0.0001). Responses to standard stimuli in the MMN paradigm were assessed using measures of alpha evoked power and inter-trial coherence (ITC). While deficits in alpha ITC were observed across sites (both p<0.05), deficits in alpha power were observed at the inpatient (p=0.001) but not outpatient (p=0.2) site. Overall, these finding indicate that impairments of frequency MMN generation and response power to standard stimuli could be particularly linked to forms of schizophrenia that are associated with poor functional outcome.
失匹配负波(MMN)产生缺陷是精神分裂症中得到最好复制的神经生理缺陷之一,其幅度的降低反映了在颞上听觉皮层水平上信息处理受损。根据偏差类型,已有研究报告了 MMN 功能障碍的不同模式,一些研究小组显示持续 MMN 受损但频率 MMN 未受损,而其他研究小组则报告了这两种发现。我们评估了这样一个假设,即招募状态,反映当前的功能状态,可能是 MMN 功能障碍模式的一个重要决定因素。在这里,我们评估了 MMN 功能障碍模式,以及来自 1)主要住院/居住护理环境(Nathan Kline Institute)和 2)主要门诊环境(哥伦比亚大学)的受试者的音调匹配和神经心理学表现。正如预测的那样,与健康对照组相比,在两个地点都观察到持续 MMN 的缺陷,而频率 MMN/音调匹配的缺陷仅限于慢性住院环境。在患者中,频率 MMN 缺陷与跨地点的音调匹配能力损伤高度相关(r=-0.52,p<0.0001),以及言语学习损伤(r=-0.54,p<0.0001)。使用 alpha 诱发功率和试验间相干性(ITC)的测量来评估 MMN 范式中的标准刺激反应。虽然在两个地点都观察到 alpha ITC 的缺陷(均 p<0.05),但在住院(p=0.001)而非门诊(p=0.2)地点观察到 alpha 功率的缺陷。总体而言,这些发现表明,频率 MMN 生成和对标准刺激的反应能力的损伤可能与与不良功能结果相关的精神分裂症形式特别相关。