Differential Patterns of Visual Sensory Alteration Underlying Face Emotion Recognition Impairment and Motion Perception Deficits in Schizophrenia and Autism Spectrum Disorder.


Journal

Biological psychiatry
ISSN: 1873-2402
Titre abrégé: Biol Psychiatry
Pays: United States
ID NLM: 0213264

Informations de publication

Date de publication:
01 10 2019
Historique:
received: 09 01 2019
revised: 16 05 2019
accepted: 20 05 2019
pubmed: 16 7 2019
medline: 2 7 2020
entrez: 15 7 2019
Statut: ppublish

Résumé

Impaired face emotion recognition (FER) and abnormal motion processing are core features in schizophrenia (SZ) and autism spectrum disorder (ASD) that have been linked to atypical activity within the visual cortex. Despite overlaps, only a few studies have directly explored convergent versus divergent neural mechanisms of altered visual processing in ASD and SZ. We employed a multimodal imaging approach to evaluate FER and motion perception in relation to functioning of subcortical and cortical visual regions. Subjects were 20 high-functioning adults with ASD, 19 patients with SZ, and 17 control participants. Behavioral measures of coherent motion sensitivity and FER along with electrophysiological and functional magnetic resonance imaging measures of visual pattern and motion processing were obtained. Resting-state functional magnetic resonance imaging was used to assess the relationship between corticocortical and thalamocortical connectivity and atypical visual processing. SZ and ASD participants had intercorrelated deficits in FER and motion sensitivity. In both groups, reduced motion sensitivity was associated with reduced functional magnetic resonance imaging activation in the occipitotemporal cortex and lower delta-band electroencephalogram power. In ASD, FER deficits correlated with hyperactivation of dorsal stream regions and increased evoked theta power. Activation of the pulvinar correlated with abnormal alpha-band modulation in SZ and ASD with under- and overmodulation, respectively, predicting increased clinical symptoms in both groups. SZ and ASD participants showed equivalent deficits in FER and motion sensitivity but markedly different profiles of physiological dysfunction. The specific pattern of deficits observed in each group may help guide development of treatments designed to downregulate versus upregulate visual processing within the respective clinical groups.

Sections du résumé

BACKGROUND
Impaired face emotion recognition (FER) and abnormal motion processing are core features in schizophrenia (SZ) and autism spectrum disorder (ASD) that have been linked to atypical activity within the visual cortex. Despite overlaps, only a few studies have directly explored convergent versus divergent neural mechanisms of altered visual processing in ASD and SZ. We employed a multimodal imaging approach to evaluate FER and motion perception in relation to functioning of subcortical and cortical visual regions.
METHODS
Subjects were 20 high-functioning adults with ASD, 19 patients with SZ, and 17 control participants. Behavioral measures of coherent motion sensitivity and FER along with electrophysiological and functional magnetic resonance imaging measures of visual pattern and motion processing were obtained. Resting-state functional magnetic resonance imaging was used to assess the relationship between corticocortical and thalamocortical connectivity and atypical visual processing.
RESULTS
SZ and ASD participants had intercorrelated deficits in FER and motion sensitivity. In both groups, reduced motion sensitivity was associated with reduced functional magnetic resonance imaging activation in the occipitotemporal cortex and lower delta-band electroencephalogram power. In ASD, FER deficits correlated with hyperactivation of dorsal stream regions and increased evoked theta power. Activation of the pulvinar correlated with abnormal alpha-band modulation in SZ and ASD with under- and overmodulation, respectively, predicting increased clinical symptoms in both groups.
CONCLUSIONS
SZ and ASD participants showed equivalent deficits in FER and motion sensitivity but markedly different profiles of physiological dysfunction. The specific pattern of deficits observed in each group may help guide development of treatments designed to downregulate versus upregulate visual processing within the respective clinical groups.

Identifiants

pubmed: 31301757
pii: S0006-3223(19)31406-4
doi: 10.1016/j.biopsych.2019.05.016
pmc: PMC7197738
mid: NIHMS1530458
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

557-567

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA003383
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH049334
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH084031
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

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Auteurs

Antígona Martínez (A)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York; Department of Psychiatry, Columbia University Medical Center, New York, New York. Electronic address: martinez@nki.rfmh.org.

Russell Tobe (R)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Elisa C Dias (EC)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Babak A Ardekani (BA)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Jeremy Veenstra-VanderWeele (J)

Department of Psychiatry, Columbia University Medical Center, New York, New York.

Gaurav Patel (G)

Department of Psychiatry, Columbia University Medical Center, New York, New York.

Melissa Breland (M)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Alexis Lieval (A)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Gail Silipo (G)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York.

Daniel C Javitt (DC)

Schizophrenia Research Division, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York; Department of Psychiatry, Columbia University Medical Center, New York, New York.

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Classifications MeSH