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Abnormally Large Baseline P300 Amplitude Is Associated With Conversion to Psychosis in Clinical High Risk Individuals With a History of Autism: A Pilot Study

机译:异常大的基线P300振幅与临床高危人员转化为具有自闭症史的临床高危人员:试点研究

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摘要

Psychosis rates in autism spectrum disorder (ASD) are 5–35% higher than in the general population. The overlap in sensory and attentional processing abnormalities highlights the possibility of related neurobiological substrates. Previous research has shown that several electroencephalography (EEG)-derived event-related potential (ERP) components that are abnormal in schizophrenia, including P300, are also abnormal in individuals at Clinical High Risk (CHR) for psychosis and predict conversion to psychosis. Yet, it is unclear whether P300 is similarly sensitive to psychosis risk in help-seeking CHR individuals with ASD history. In this exploratory study, we leveraged data from the North American Prodrome Longitudinal Study (NAPLS2) to probe for the first time EEG markers of longitudinal psychosis profiles in ASD. Specifically, we investigated the P300 ERP component and its sensitivity to psychosis conversion across CHR groups with (ASD+) and without (ASD–) comorbid ASD. Baseline EEG data were analyzed from 304 CHR patients (14 ASD+; 290 ASD–) from the NAPLS2 cohort who were followed longitudinally over two years. We examined P300 amplitude to infrequent Target (10%; P3b) and Novel distractor (10%; P3a) stimuli from visual and auditory oddball tasks. Whereas P300 amplitude attenuation is typically characteristic of CHR and predictive of conversion to psychosis in non-ASD sample, in our sample, history of ASD moderated this relationship such that, in CHR/ASD+ individuals, enhanced – rather than attenuated - visual P300 (regardless of stimulus type) was associated with psychosis conversion. This pattern was also seen for auditory P3b amplitude to Target stimuli. Though drawn from a small sample of CHR individuals with ASD, these preliminary results point to a paradoxical effect, wherein those with both CHR and ASD history who go on to develop psychosis have a unique pattern of enhanced neural response during attention orienting to both visual and target stimuli. Such a pattern stands out from the usual finding of P300 amplitude reductions predicting psychosis in non-ASD CHR populations and warrants follow up in larger scale, targeted, longitudinal studies of those with ASD at clinical high risk for psychosis.
机译:自闭症谱系障碍(ASD)的精神病率比一般人群高5-35%。感觉和注意力处理异常的重叠突出了相关神经生物学基质的可能性。以前的研究表明,在精神分裂症(包括P300)的若干脑电图(脑电图)相关的相关电位(ERP)组分,包括P300,在临床高风险(CHR)中的个体上也异常,用于精神病,并预测对精神病症的转化。然而,目前尚不清楚P300是否与有关ASD历史的帮助征收CHR个人的精神病风险类似地敏感。在这项探索性研究中,我们利用北美产品纵向研究(NAPLS2)的数据来探讨ASD中的纵向精神病谱的第一次脑电图。具体而言,我们研究了P300 ERP组分及其对具有(ASD +)和无(ASD-)COMORBID ASD的CHR组的精神病转换敏感性。从304年CHR患者(14 ASD +; 290 ASD-)分析了基线EEG数据,从两年内完成了纵向的NAPLS2群体。我们检查了P300振幅,以罕见的目标(10%; P3B)和来自视觉和听觉奇怪的任务的小说分心(10%; P3A)刺激。而P300幅度衰减通常是CHR的特征,并且在非ASD样本中对心理到精神病的预测性,在我们的样本中,ASD的历史使这一关系中的历史如此,在CHR / ASD +个人中,增强 - 而不是减弱 - Visual P300(无论如何)刺激型)与精神病转换有关。还可以看到这种模式用于对靶刺激的听觉P3b振幅。虽然从带有ASD的CHR个体样本中汲取的,但这些初步结果指向矛盾的效果,其中与CHR和ASD历史的人继续开发精神病的历史上有一种独特的神经反应在对视觉和视觉上的提高神经响应的独特模式。目标刺激。这种模式从通常的发现P300幅度减少预测非ASD CHR人口中的精神病,并且在临床高风险上以更大规模,纵向研究的较大规模,目标,纵向研究的权证进行跟进。

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