4.7 Article

Automatic auditory processing features in distinct subtypes of patients at clinical high risk for psychosis: Forecasting remission with mismatch negativity

期刊

HUMAN BRAIN MAPPING
卷 43, 期 18, 页码 5452-5464

出版社

WILEY
DOI: 10.1002/hbm.26021

关键词

event-related spectral perturbation; inter-trial coherence; mismatch negativity; remission; subtypes; ultra-high risk

资金

  1. National Natural Science Foundation of China [82151314, 81901832, 81871050, 82171497]
  2. Science and Technology Commission of Shanghai Municipality [19441907800, 19ZR1445200, 17411953100, 16JC1420200, 2018SHZDZX01, 19410710800, 19411969100, 19411950800]
  3. Shanghai Clinical Research Center for Mental Health [19MC1911100]
  4. Clinical Research Center at Shanghai Mental Health Center [CRC2018ZD01, CRC2018ZD04]
  5. To the youth Psychological class for middle school students [21DZ2300400]

向作者/读者索取更多资源

Individuals at clinical high risk for psychosis exhibit dysfunctions in pre-attentive deviance processing, as indicated by compromised mismatch negativity (MMN) response. This study investigated the association between event-related potential and time-frequency information with clinical profiles in CHR individuals, and identified predictive indices for remission. The findings suggest disrupted automatic auditory processing in certain CHR subtypes and the potential of MMN response as a neurophysiological marker for distinct clinical subtypes.
Individuals at clinical high risk (CHR) for psychosis exhibit a compromised mismatch negativity (MMN) response, which indicates dysfunction of pre-attentive deviance processing. Event-related potential and time-frequency (TF) information, in combination with clinical and cognitive profiles, may provide insight into the pathophysiology and psychopathology of the CHR stage and predict the prognosis of CHR individuals. A total of 92 individuals with CHR were recruited and followed up regularly for up to 3 years. Individuals with CHR were classified into three clinical subtypes demonstrated previously, specifically 28 from Cluster 1 (characterized by extensive negative symptoms and cognitive deficits), 31 from Cluster 2 (characterized by thought and behavioral disorganization, with moderate cognitive impairment), and 33 from Cluster 3 (characterized by the mildest symptoms and cognitive deficits). Auditory MMN to frequency and duration deviants was assessed. The event-related spectral perturbation (ERSP) and inter-trial coherence (ITC) were acquired using TF analysis. Predictive indices for remission were identified using logistic regression analyses. As expected, reduced frequency MMN (fMMN) and duration MMN (dMMN) responses were noted in Cluster 1 relative to the other two clusters. In the TF analysis, Cluster 1 showed decreased theta and alpha ITC in response to deviant stimuli. The regression analyses revealed that dMMN latency and alpha ERSP to duration deviants, theta ITC to frequency deviants and alpha ERSP to frequency deviants, and fMMN latency were significant MMN predictors of remission for the three clusters. MMN variables outperformed behavioral variables in predicting remission of Clusters 1 and 2. Our findings indicate relatively disrupted automatic auditory processing in a certain CHR subtype and a close affinity between these electrophysiological indexes and clinical profiles within different clusters. Furthermore, MMN indexes may serve as predictors of subsequent remission from the CHR state. These findings suggest that the auditory MMN response is a potential neurophysiological marker for distinct clinical subtypes of CHR.

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