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Thalamic dysconnectivity in the psychosis risk syndrome and early illness schizophrenia

Published online by Cambridge University Press:  15 March 2021

Susanna L. Fryer
Affiliation:
Department of Psychiatry, University of California, San Francisco, San Francisco, CA, USA San Francisco VA Healthcare System, San Francisco, CA, USA
Jamie M. Ferri
Affiliation:
San Francisco VA Healthcare System, San Francisco, CA, USA
Brian J. Roach
Affiliation:
San Francisco VA Healthcare System, San Francisco, CA, USA
Rachel L. Loewy
Affiliation:
Department of Psychiatry, University of California, San Francisco, San Francisco, CA, USA
Barbara K. Stuart
Affiliation:
Department of Psychiatry, University of California, San Francisco, San Francisco, CA, USA
Alan Anticevic
Affiliation:
Department of Psychiatry, Yale School of Medicine, New Haven, CT, USA Department of Psychology, Yale University, New Haven, CT, USA
Judith M. Ford
Affiliation:
Department of Psychiatry, University of California, San Francisco, San Francisco, CA, USA San Francisco VA Healthcare System, San Francisco, CA, USA
Daniel H. Mathalon*
Affiliation:
Department of Psychiatry, University of California, San Francisco, San Francisco, CA, USA San Francisco VA Healthcare System, San Francisco, CA, USA
*
Author for correspondence: Daniel H. Mathalon, E-mail: [email protected]

Abstract

Background

Schizophrenia (SZ) is associated with thalamic dysconnectivity. Compared to healthy controls (HCs), individuals with SZ have hyperconnectivity with sensory regions, and hypoconnectivity with cerebellar, thalamic, and prefrontal regions. Despite replication of this pattern in chronically ill individuals, less is known about when these abnormalities emerge in the illness course and if they are present prior to illness onset.

Methods

Resting-state functional magnetic resonance imaging data were collected from psychosis risk syndrome (PRS) youth (n = 45), early illness SZ (ESZ) (n = 74) patients, and HCs (n = 85). Age-adjusted functional connectivity, seeded from the thalamus, was compared among the groups.

Results

Significant effects of group were observed in left and right middle temporal regions, left and right superior temporal regions, left cerebellum, and bilateral thalamus. Compared to HCs, ESZ demonstrated hyperconnectivity to all temporal lobe regions and reduced connectivity with cerebellar, anterior cingulate, and thalamic regions. Compared to HCs, PRS demonstrated hyperconnectivity with the left and right middle temporal regions, and hypoconnectivity with the cerebellar and other thalamic regions. Compared to PRS participants, ESZ participants were hyperconnected to temporal regions, but did not differ from PRS in hypoconnectivity with cerebellar and thalamic regions. Thalamic dysconnectivity was unrelated to positive symptom severity in ESZ or PRS groups.

Conclusions

PRS individuals demonstrated an intermediate level of thalamic dysconnectivity, whereas ESZ showed a pattern consistent with prior observations in chronic samples. These cross-sectional findings suggest that thalamic dysconnectivity may occur prior to illness onset and become more pronounced in early illness stages.

Type
Original Article
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press

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Footnotes

*

Co-first authors.

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