A machine-learning approach for differentiating borderline personality disorder from community participants with brain-wide functional connectivity.

BPD Borderline personality disorder Classification Functional connectivity Multivariate fMRI

Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
26 May 2024
Historique:
received: 22 01 2024
revised: 23 05 2024
accepted: 24 05 2024
medline: 29 5 2024
pubmed: 29 5 2024
entrez: 28 5 2024
Statut: aheadofprint

Résumé

Functional connectivity has garnered interest as a potential biomarker of psychiatric disorders including borderline personality disorder (BPD). However, small sample sizes and lack of within-study replications have led to divergent findings with no clear spatial foci. Evaluate discriminative performance and generalizability of functional connectivity markers for BPD. Whole-brain fMRI resting state functional connectivity in matched subsamples of 116 BPD and 72 control individuals defined by three grouping strategies. We predicted BPD status using classifiers with repeated cross-validation based on multiscale functional connectivity within and between regions of interest (ROIs) covering the whole brain-global ROI-based network, seed-based ROI-connectivity, functional consistency, and voxel-to-voxel connectivity-and evaluated the generalizability of the classification in the left-out portion of non-matched data. Full-brain connectivity allowed classification (~70 %) of BPD patients vs. controls in matched inner cross-validation. The classification remained significant when applied to unmatched out-of-sample data (~61-70 %). Highest seed-based accuracies were in a similar range to global accuracies (~70-75 %), but spatially more specific. The most discriminative seed regions included midline, temporal and somatomotor regions. Univariate connectivity values were not predictive of BPD after multiple comparison corrections, but weak local effects coincided with the most discriminative seed-ROIs. Highest accuracies were achieved with a full clinical interview while self-report results remained at chance level. The accuracies vary considerably between random sub-samples of the population, global signal and covariates limiting the practical applicability. Spatially distributed functional connectivity patterns are moderately predictive of BPD despite heterogeneity of the patient population.

Sections du résumé

BACKGROUND BACKGROUND
Functional connectivity has garnered interest as a potential biomarker of psychiatric disorders including borderline personality disorder (BPD). However, small sample sizes and lack of within-study replications have led to divergent findings with no clear spatial foci.
AIMS OBJECTIVE
Evaluate discriminative performance and generalizability of functional connectivity markers for BPD.
METHOD METHODS
Whole-brain fMRI resting state functional connectivity in matched subsamples of 116 BPD and 72 control individuals defined by three grouping strategies. We predicted BPD status using classifiers with repeated cross-validation based on multiscale functional connectivity within and between regions of interest (ROIs) covering the whole brain-global ROI-based network, seed-based ROI-connectivity, functional consistency, and voxel-to-voxel connectivity-and evaluated the generalizability of the classification in the left-out portion of non-matched data.
RESULTS RESULTS
Full-brain connectivity allowed classification (~70 %) of BPD patients vs. controls in matched inner cross-validation. The classification remained significant when applied to unmatched out-of-sample data (~61-70 %). Highest seed-based accuracies were in a similar range to global accuracies (~70-75 %), but spatially more specific. The most discriminative seed regions included midline, temporal and somatomotor regions. Univariate connectivity values were not predictive of BPD after multiple comparison corrections, but weak local effects coincided with the most discriminative seed-ROIs. Highest accuracies were achieved with a full clinical interview while self-report results remained at chance level.
LIMITATIONS CONCLUSIONS
The accuracies vary considerably between random sub-samples of the population, global signal and covariates limiting the practical applicability.
CONCLUSIONS CONCLUSIONS
Spatially distributed functional connectivity patterns are moderately predictive of BPD despite heterogeneity of the patient population.

Identifiants

pubmed: 38806064
pii: S0165-0327(24)00868-1
doi: 10.1016/j.jad.2024.05.125
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors report no conflicts of interest.

Auteurs

Juha M Lahnakoski (JM)

Independent Max Planck Research Group for Social Neuroscience, Max Planck Institute of Psychiatry, Munich, Germany; Institute of Neuroscience and Medicine, Brain & Behaviour (INM-7), Research Center Jülich, Wilhelm-Johnen-Straße, 52428 Jülich, Germany; Institute of Systems Neuroscience, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr. 5, 40225 Düsseldorf, Germany. Electronic address: j.lahnakoski@fz-juelich.de.

Tobias Nolte (T)

Wellcome Trust Centre for Neuroimaging, University College London, London, United Kingdom; Anna Freud National Centre for Children and Families, London, United Kingdom.

Alec Solway (A)

Fralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA.

Iris Vilares (I)

Department of Psychology, University of Minnesota, Minneapolis, MN, USA.

Andreas Hula (A)

Austrian Institute of Technology, Vienna, Austria.

Janet Feigenbaum (J)

Research Department of Clinical, Educational and Health Psychology, University College London, London, United Kingdom.

Terry Lohrenz (T)

Fralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA.

Brooks King-Casas (B)

Fralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA; Department of Psychology, Virginia Tech, Blacksburg, VA, USA.

Peter Fonagy (P)

Anna Freud National Centre for Children and Families, London, United Kingdom; Research Department of Clinical, Educational and Health Psychology, University College London, London, United Kingdom.

P Read Montague (PR)

Wellcome Trust Centre for Neuroimaging, University College London, London, United Kingdom; Fralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA; Department of Physics, Virginia Tech, Blacksburg, VA, USA; Department of Psychiatry and Behavioral Medicine, Virginia Tech Carilion School of Medicine, Virginia Tech, Roanoke, VA, USA.

Leonhard Schilbach (L)

Independent Max Planck Research Group for Social Neuroscience, Max Planck Institute of Psychiatry, Munich, Germany; Department of Psychiatry, Ludwig-Maximilians-Universität, Munich, Germany.

Classifications MeSH