社会环境下精神分裂症患者NoGo P300 ERP的改变:一项超扫描研究。

IF 6.2 1区 医学 Q1 PSYCHIATRY
Máté Fullajtár, Brigitta Kakuszi, István Bitter, Pál Czobor
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引用次数: 0

摘要

虽然精神分裂症患者在社会认知方面表现出严重的缺陷,但对这些缺陷的神经生物学背景的研究是在孤立的单人环境中进行的。我们研究了社会环境中社会认知缺陷的神经生物学基础,采用了一种新的方法——脑电图超扫描。80名受试者被纳入分析,49名健康对照(HC)和31名精神分裂症患者。我们记录了成对参与者的高密度脑电图,其中一个(观察者)看着自己的屏幕,而另一个(演员)积极地执行Go/NoGo任务。这项任务进行了两次,参与者互换了角色。我们主要从观察者条件研究P300事件相关电位。采用PANSS量表对精神病理进行表征。采用眼读心术测试和d-prime指数来表征心智化和信号检测能力。我们发现,与HC组相比,精神分裂症患者在第一次任务暴露时P300显著降低。然而,随着反复暴露,它们表现出P300的增强,而hc则表现出下降。在两项任务暴露中,更严重的阳性症状与较大的P300相关。此外,较差的心智化和信号检测性能与P300下降有关。我们的研究结果提供了P300在精神分裂症中的改变可以在社会环境中检测到的证据。两组中相反的变化可能是由于完全不同的原因:hc的习惯化,而患者的变化可能是由各种因素引起的,包括习惯化不足和在社会环境中对刺激显著性的异常处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alterations of NoGo P300 ERP in schizophrenia in social setting: a hyperscanning study.

Alterations of NoGo P300 ERP in schizophrenia in social setting: a hyperscanning study.

Alterations of NoGo P300 ERP in schizophrenia in social setting: a hyperscanning study.

Alterations of NoGo P300 ERP in schizophrenia in social setting: a hyperscanning study.

Although patients with schizophrenia exhibit profound deficits in social cognition, studies into the neurobiological background of these deficits examined individuals in isolation, in single-person settings. We investigated the neurobiological basis of social cognitive deficits in a social setting, applying a novel approach using EEG-hyperscanning. Eighty subjects were included in the analyses, 49 healthy controls (HC) and 31 patients with schizophrenia. We recorded high-density EEG from pairs of participants, where one (the observer) watched their own screen while the other (the actor) actively performed a Go/NoGo task. The task was administered twice, with the participants switching roles. We focused on investigating the P300 event-related potential from the observer condition. The PANSS scale was used to characterize psychopathology. The Reading the Mind in the Eyes Test and the d-prime index were applied to characterize mentalization and signal detection ability. We found that patients with schizophrenia showed significant P300 reduction compared to the HC group at the first task exposure. They, however, exhibited augmented P300 with the repeated exposure, while HCs manifested a decrease. More severe positive symptoms were associated with larger P300 at both task-exposures. Moreover, poorer mentalization and signal detection performance were associated with decreased P300. Our findings provide evidence that P300 alterations in schizophrenia can be detected in social setting. The opposite changes in the two groups may be due to disparate reasons: habituation in HCs, whereas the alterations in patients may result from various factors, including deficient habituation and an aberrant processing of stimulus salience in a social setting.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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