Predicting individual improvement in schizophrenia symptom severity at 1-year follow-up: Comparison of connectomic, structural, and clinical predictors.


Journal

Human brain mapping
ISSN: 1097-0193
Titre abrégé: Hum Brain Mapp
Pays: United States
ID NLM: 9419065

Informations de publication

Date de publication:
15 08 2020
Historique:
received: 06 07 2019
revised: 13 01 2020
accepted: 13 04 2020
pubmed: 30 5 2020
medline: 15 12 2021
entrez: 30 5 2020
Statut: ppublish

Résumé

In a machine learning setting, this study aims to compare the prognostic utility of connectomic, brain structural, and clinical/demographic predictors of individual change in symptom severity in individuals with schizophrenia. Symptom severity at baseline and 1-year follow-up was assessed in 30 individuals with a schizophrenia-spectrum disorder using the Brief Psychiatric Rating Scale. Structural and functional neuroimaging was acquired in all individuals at baseline. Machine learning classifiers were trained to predict whether individuals improved or worsened with respect to positive, negative, and overall symptom severity. Classifiers were trained using various combinations of predictors, including regional cortical thickness and gray matter volume, static and dynamic resting-state connectivity, and/or baseline clinical and demographic variables. Relative change in overall symptom severity between baseline and 1-year follow-up varied markedly among individuals (interquartile range: 55%). Dynamic resting-state connectivity measured within the default-mode network was the most accurate single predictor of change in positive (accuracy: 87%), negative (83%), and overall symptom severity (77%) at follow-up. Incorporating predictors based on regional cortical thickness, gray matter volume, and baseline clinical variables did not markedly improve prediction accuracy and the prognostic utility of these predictors in isolation was moderate (<70%). Worsening negative symptoms at 1-year follow-up were predicted by hyper-connectivity and hypo-dynamism within the default-mode network at baseline assessment, while hypo-connectivity and hyper-dynamism predicted worsening positive symptoms. Given the modest sample size investigated, we recommend giving precedence to the relative ranking of the predictors investigated in this study, rather than the prediction accuracy estimates.

Identifiants

pubmed: 32469448
doi: 10.1002/hbm.25020
pmc: PMC7375115
doi:

Substances chimiques

Antipsychotic Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3342-3357

Subventions

Organisme : NHMRC
ID : APP1138711
Organisme : NHMRC
ID : APP1099082
Organisme : NHMRC
ID : APP1136649
Organisme : NHMRC
ID : 1105825
Organisme : NHMRC
ID : 628386
Organisme : NHMRC
ID : 628880
Organisme : University of Melbourne Early Career Researcher
ID : 601253
Organisme : Australian National Health and Medical Research Council (NHMRC)
ID : 1065742

Informations de copyright

© 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc.

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Auteurs

Akhil Kottaram (A)

Department of Biomedical Engineering, The University of Melbourne, Melbourne, Victoria, Australia.
Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.

Leigh A Johnston (LA)

Department of Biomedical Engineering, The University of Melbourne, Melbourne, Victoria, Australia.
Melbourne Brain Centre Imaging Unit, The University of Melbourne, Melbourne, Victoria, Australia.

Ye Tian (Y)

Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia.

Eleni P Ganella (EP)

Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia.
Cooperative Research Centre for Mental Health, Carlton, Victoria, Australia.

Liliana Laskaris (L)

Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia.
Centre for Neural Engineering, Department of Electrical and Electronic Engineering, The University of Melbourne, Melbourne, Victoria, Australia.

Luca Cocchi (L)

Clinical Brain Networks Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Patrick McGorry (P)

Orygen, Parkville, Victoria, Australia.
Centre for Youth Mental Health, The University of Melbourne, Parkville, Victoria, Australia.

Christos Pantelis (C)

Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia.
Cooperative Research Centre for Mental Health, Carlton, Victoria, Australia.
Centre for Neural Engineering, Department of Electrical and Electronic Engineering, The University of Melbourne, Melbourne, Victoria, Australia.
North Western Mental Health, Melbourne Health, Parkville, Victoria, Australia.
Florey Institute for Neurosciences and Mental Health, Parkville, Victoria, Australia.

Ramamohanarao Kotagiri (R)

Department of Computing and Information Systems, The University of Melbourne, Melbourne, Victoria, Australia.

Vanessa Cropley (V)

Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.
Department of Psychiatry, The University of Melbourne, Melbourne, Victoria, Australia.
Centre for Mental Health, Faculty of Health, Arts and Design, School of Health Sciences, Swinburne University, Hawthorn, Victoria, Australia.

Andrew Zalesky (A)

Department of Biomedical Engineering, The University of Melbourne, Melbourne, Victoria, Australia.
Melbourne Neuropsychiatry Centre, The University of Melbourne, Melbourne, Victoria, Australia.

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