» Articles » PMID: 20826078

Neuroanatomical Correlates of Executive Dysfunction in the At-risk Mental State for Psychosis

Overview
Journal Schizophr Res
Specialty Psychiatry
Date 2010 Sep 10
PMID 20826078
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Deficits in executive functioning have been described as a core feature of schizophrenia and have been linked to patterns of fronto-temporo-limbic brain alterations. To date, such structure-cognition relationships have not been explored in a clinically defined at-risk mental state (ARMS) for psychosis using whole-brain neuroimaging techniques. Therefore, we used voxel-based morphometry in 40 ARMS and 30 matched healthy control (HC) individuals to investigate whether gray and white matter volumes (1) correlated with the performance in the Trail-Making Test B (TMT-B), an established measure of executive functioning, and (2) were volumetrically linked to the ventromedial prefrontal cortex (VMPFC), found to be associated with TMT-B in the ARMS during the first analysis step. We found the ARMS subjects to be specifically impaired in their TMT-B performance versus HC. Brain-cognition associations involving the insular cortices were observed in the HC, but not in the ARMS individuals. Conversely, TMT-B correlations in the VMPFC, the cerebellum, the fronto-callosal white matter were detected in the ARMS, but not the HC group. The VMPFC was linked to the temporo-limbic cortices in HC, whereas the connectivity pattern in the ARMS involved the left temporal and dorsolateral prefrontal cortex, the cerebellum, the right SMA and extended portions of the fronto-callosal white matter. These findings suggest that executive deficits are already present in the ARMS for psychosis and may be subserved by structurally altered networks of interconnected cortical and subcortical brain regions in line with the disconnectivity hypothesis of schizophrenia.

Citing Articles

Cognitive subgroups of affective and non-affective psychosis show differences in medication and cortico-subcortical brain networks.

Bracher K, Wohlschlaeger A, Koch K, Knolle F Sci Rep. 2024; 14(1):20314.

PMID: 39223185 PMC: 11369100. DOI: 10.1038/s41598-024-71316-3.


Cognitive Dysfunction as a Risk Factor for Psychosis.

Karcher N, Merchant J, Pine J, Kilciksiz C Curr Top Behav Neurosci. 2022; 63:173-203.

PMID: 35989398 DOI: 10.1007/7854_2022_387.


Hippocampal structural alterations in early-stage psychosis: Specificity and relationship to clinical outcomes.

Brunner G, Gajwani R, Gross J, Gumley A, Krishnadas R, Lawrie S Neuroimage Clin. 2022; 35:103087.

PMID: 35780662 PMC: 9421451. DOI: 10.1016/j.nicl.2022.103087.


Generalized neurocognitive impairment in individuals at ultra-high risk for psychosis: The possible key role of slowed processing speed.

Randers L, Jepsen J, Fagerlund B, Nordholm D, Krakauer K, Hjorthoj C Brain Behav. 2021; 11(3):e01962.

PMID: 33486897 PMC: 7994693. DOI: 10.1002/brb3.1962.


Relational Memory in the Early Stage of Psychosis: A 2-Year Follow-up Study.

Avery S, Armstrong K, McHugo M, Vandekar S, Blackford J, Woodward N Schizophr Bull. 2020; 47(1):75-86.

PMID: 32657351 PMC: 7825006. DOI: 10.1093/schbul/sbaa081.