Longitudinal Assessment and Functional Neuroimaging of Movement Variability Reveal Novel Insights Into Motor Dysfunction in Clinical High Risk for Psychosis

Author:

Dean Derek J1ORCID,Bernard Jessica A23,Damme Katherine S F4,O’Reilly Randall5,Orr Joseph M23,Mittal Vijay A46789

Affiliation:

1. Department of Psychology, Vanderbilt University, Nashville, TN

2. Department of Psychological and Brain Sciences, Texas A&M University, College Station, TX

3. Institute for Neuroscience, Texas A&M University, College Station, TX

4. Department of Psychology, Northwestern University, Evanston, IL

5. Departments of Psychology, Computer Science, and Center for Neuroscience, University of California Davis, Davis, CA

6. Department of Psychiatry, Northwestern University, Chicago IL

7. Institute for Policy Research, Northwestern University, Evanston, IL

8. Department of Medical Social Sciences, Northwestern University, Chicago, IL

9. Institute for Innovations in Developmental Sciences, Northwestern University, Evanston/Chicago, IL

Abstract

Abstract Motor dysfunction in youth at clinical high risk (CHR) for psychosis is thought to reflect abnormal neurodevelopment within cortical-subcortical motor circuits and may be important for understanding clinical trajectories of CHR individuals. However, to date, our perspective of brain-behavior relationships has been informed solely by cross-sectional correlational studies linking behavior in the lab to brain structure or respective resting-state network connectivity. Here, we assess movement dysfunction from 2 perspectives: study 1 investigates the longitudinal progression of handwriting variability and positive symptoms in a sample of 91 CHR and healthy controls during a 12-month follow-up and study 2 involves a multiband functional magnetic resonance imaging task exploring the relationship between power grip force stability and motor network brain activation in a subset of participants. In study 1, we found that greater handwriting variability was a stable feature of CHR participants who experienced worse symptom progression. Study 2 results showed that CHR individuals had greater variability in their grip force and greater variability was related to decreased activation in the associative cortico-striatal network compared to controls. Motor variability may be a stable marker of vulnerability for psychosis risk and possible indicator of a vulnerable cortico-striatal brain network functioning in CHR participants, although the effects of antipsychotic medication should be considered.

Funder

Brain and Behavior Research Foundation

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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