Exploring neural dysfunction in 'clinical high risk' for psychosis: A quantitative review of fMRI studies

Anirban Dutt, Huai-Hsuan Tseng, Leon Fonville, Mark Drakesmith, Liang Su, John Evans, Stanley Zammit, Derek Jones, Glyn Lewis, Anthony S. David

Research output: Contribution to journalReview article

18 Citations (Scopus)

Abstract

Individuals at clinical high risk (CHR) of developing psychosis present with widespread functional abnormalities in the brain. Cognitive deficits, including working memory (WM) problems, as commonly elicited by n-back tasks, are observed in CHR individuals. However, functional MRI (fMRI) studies, comprising a heterogeneous cluster of general and social cognition paradigms, have not necessarily demonstrated consistent and conclusive results in this population. Hence, a comprehensive review of fMRI studies, spanning almost one decade, was carried out to observe for general trends with respect to brain regions and cognitive systems most likely to be dysfunctional in CHR individuals. 32 studies were included for this review, out of which 22 met the criteria for quantitative analysis using activation likelihood estimation (ALE). Task related contrast activations were firstly analysed by comparing CHR and healthy control participants in the total pooled sample, followed by a comparison of general cognitive function studies (excluding social cognition paradigms), and finally by only looking at n-back working memory task based studies. Findings from the ALE implicated four key dysfunctional and distinct neural regions in the CHR group, namely the right inferior parietal lobule (rIPL), the left medial frontal gyrus (lmFG), the left superior temporal gyrus (lSTG) and the right fronto-polar cortex (rFPC) of the superior frontal gyrus (SFG). Narrowing down to relatively few significant dysfunctional neural regions is a step forward in reducing the apparent ambiguity of overall findings, which would help to target specific neural regions and pathways of interest for future research in CHR populations.

Original languageEnglish
Pages (from-to)122-134
Number of pages13
JournalJournal of Psychiatric Research
Volume61
DOIs
Publication statusPublished - 2015 Feb 1

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Psychotic Disorders
Magnetic Resonance Imaging
Cognition
Prefrontal Cortex
Short-Term Memory
Activation Analysis
Neural Pathways
Parietal Lobe
Brain
Temporal Lobe
Population
Healthy Volunteers

All Science Journal Classification (ASJC) codes

  • Psychiatry and Mental health
  • Biological Psychiatry

Cite this

Dutt, Anirban ; Tseng, Huai-Hsuan ; Fonville, Leon ; Drakesmith, Mark ; Su, Liang ; Evans, John ; Zammit, Stanley ; Jones, Derek ; Lewis, Glyn ; David, Anthony S. / Exploring neural dysfunction in 'clinical high risk' for psychosis : A quantitative review of fMRI studies. In: Journal of Psychiatric Research. 2015 ; Vol. 61. pp. 122-134.
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Exploring neural dysfunction in 'clinical high risk' for psychosis : A quantitative review of fMRI studies. / Dutt, Anirban; Tseng, Huai-Hsuan; Fonville, Leon; Drakesmith, Mark; Su, Liang; Evans, John; Zammit, Stanley; Jones, Derek; Lewis, Glyn; David, Anthony S.

In: Journal of Psychiatric Research, Vol. 61, 01.02.2015, p. 122-134.

Research output: Contribution to journalReview article

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T1 - Exploring neural dysfunction in 'clinical high risk' for psychosis

T2 - A quantitative review of fMRI studies

AU - Dutt, Anirban

AU - Tseng, Huai-Hsuan

AU - Fonville, Leon

AU - Drakesmith, Mark

AU - Su, Liang

AU - Evans, John

AU - Zammit, Stanley

AU - Jones, Derek

AU - Lewis, Glyn

AU - David, Anthony S.

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N2 - Individuals at clinical high risk (CHR) of developing psychosis present with widespread functional abnormalities in the brain. Cognitive deficits, including working memory (WM) problems, as commonly elicited by n-back tasks, are observed in CHR individuals. However, functional MRI (fMRI) studies, comprising a heterogeneous cluster of general and social cognition paradigms, have not necessarily demonstrated consistent and conclusive results in this population. Hence, a comprehensive review of fMRI studies, spanning almost one decade, was carried out to observe for general trends with respect to brain regions and cognitive systems most likely to be dysfunctional in CHR individuals. 32 studies were included for this review, out of which 22 met the criteria for quantitative analysis using activation likelihood estimation (ALE). Task related contrast activations were firstly analysed by comparing CHR and healthy control participants in the total pooled sample, followed by a comparison of general cognitive function studies (excluding social cognition paradigms), and finally by only looking at n-back working memory task based studies. Findings from the ALE implicated four key dysfunctional and distinct neural regions in the CHR group, namely the right inferior parietal lobule (rIPL), the left medial frontal gyrus (lmFG), the left superior temporal gyrus (lSTG) and the right fronto-polar cortex (rFPC) of the superior frontal gyrus (SFG). Narrowing down to relatively few significant dysfunctional neural regions is a step forward in reducing the apparent ambiguity of overall findings, which would help to target specific neural regions and pathways of interest for future research in CHR populations.

AB - Individuals at clinical high risk (CHR) of developing psychosis present with widespread functional abnormalities in the brain. Cognitive deficits, including working memory (WM) problems, as commonly elicited by n-back tasks, are observed in CHR individuals. However, functional MRI (fMRI) studies, comprising a heterogeneous cluster of general and social cognition paradigms, have not necessarily demonstrated consistent and conclusive results in this population. Hence, a comprehensive review of fMRI studies, spanning almost one decade, was carried out to observe for general trends with respect to brain regions and cognitive systems most likely to be dysfunctional in CHR individuals. 32 studies were included for this review, out of which 22 met the criteria for quantitative analysis using activation likelihood estimation (ALE). Task related contrast activations were firstly analysed by comparing CHR and healthy control participants in the total pooled sample, followed by a comparison of general cognitive function studies (excluding social cognition paradigms), and finally by only looking at n-back working memory task based studies. Findings from the ALE implicated four key dysfunctional and distinct neural regions in the CHR group, namely the right inferior parietal lobule (rIPL), the left medial frontal gyrus (lmFG), the left superior temporal gyrus (lSTG) and the right fronto-polar cortex (rFPC) of the superior frontal gyrus (SFG). Narrowing down to relatively few significant dysfunctional neural regions is a step forward in reducing the apparent ambiguity of overall findings, which would help to target specific neural regions and pathways of interest for future research in CHR populations.

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