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Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach

BACKGROUND: Bipolar disorder (BD) is one of the leading causes of disability worldwide. Patients are further disadvantaged by delays in accurate diagnosis ranging between 5 and 10 years. We applied Gaussian process classifiers (GPCs) to structural magnetic resonance imaging (sMRI) data to evaluate t...

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Autores principales: Rocha-Rego, V., Jogia, J., Marquand, A. F., Mourao-Miranda, J., Simmons, A., Frangou, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880067/
https://www.ncbi.nlm.nih.gov/pubmed/23734914
http://dx.doi.org/10.1017/S0033291713001013
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author Rocha-Rego, V.
Jogia, J.
Marquand, A. F.
Mourao-Miranda, J.
Simmons, A.
Frangou, S.
author_facet Rocha-Rego, V.
Jogia, J.
Marquand, A. F.
Mourao-Miranda, J.
Simmons, A.
Frangou, S.
author_sort Rocha-Rego, V.
collection PubMed
description BACKGROUND: Bipolar disorder (BD) is one of the leading causes of disability worldwide. Patients are further disadvantaged by delays in accurate diagnosis ranging between 5 and 10 years. We applied Gaussian process classifiers (GPCs) to structural magnetic resonance imaging (sMRI) data to evaluate the feasibility of using pattern recognition techniques for the diagnostic classification of patients with BD. METHOD: GPCs were applied to gray (GM) and white matter (WM) sMRI data derived from two independent samples of patients with BD (cohort 1: n = 26; cohort 2: n = 14). Within each cohort patients were matched on age, sex and IQ to an equal number of healthy controls. RESULTS: The diagnostic accuracy of the GPC for GM was 73% in cohort 1 and 72% in cohort 2; the sensitivity and specificity of the GM classification were respectively 69% and 77% in cohort 1 and 64% and 99% in cohort 2. The diagnostic accuracy of the GPC for WM was 69% in cohort 1 and 78% in cohort 2; the sensitivity and specificity of the WM classification were both 69% in cohort 1 and 71% and 86% respectively in cohort 2. In both samples, GM and WM clusters discriminating between patients and controls were localized within cortical and subcortical structures implicated in BD. CONCLUSIONS: Our results demonstrate the predictive value of neuroanatomical data in discriminating patients with BD from healthy individuals. The overlap between discriminative networks and regions implicated in the pathophysiology of BD supports the biological plausibility of the classifiers.
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spelling pubmed-38800672014-01-03 Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach Rocha-Rego, V. Jogia, J. Marquand, A. F. Mourao-Miranda, J. Simmons, A. Frangou, S. Psychol Med Original Articles BACKGROUND: Bipolar disorder (BD) is one of the leading causes of disability worldwide. Patients are further disadvantaged by delays in accurate diagnosis ranging between 5 and 10 years. We applied Gaussian process classifiers (GPCs) to structural magnetic resonance imaging (sMRI) data to evaluate the feasibility of using pattern recognition techniques for the diagnostic classification of patients with BD. METHOD: GPCs were applied to gray (GM) and white matter (WM) sMRI data derived from two independent samples of patients with BD (cohort 1: n = 26; cohort 2: n = 14). Within each cohort patients were matched on age, sex and IQ to an equal number of healthy controls. RESULTS: The diagnostic accuracy of the GPC for GM was 73% in cohort 1 and 72% in cohort 2; the sensitivity and specificity of the GM classification were respectively 69% and 77% in cohort 1 and 64% and 99% in cohort 2. The diagnostic accuracy of the GPC for WM was 69% in cohort 1 and 78% in cohort 2; the sensitivity and specificity of the WM classification were both 69% in cohort 1 and 71% and 86% respectively in cohort 2. In both samples, GM and WM clusters discriminating between patients and controls were localized within cortical and subcortical structures implicated in BD. CONCLUSIONS: Our results demonstrate the predictive value of neuroanatomical data in discriminating patients with BD from healthy individuals. The overlap between discriminative networks and regions implicated in the pathophysiology of BD supports the biological plausibility of the classifiers. Cambridge University Press 2014-02 2013-06-05 /pmc/articles/PMC3880067/ /pubmed/23734914 http://dx.doi.org/10.1017/S0033291713001013 Text en © Cambridge University Press 2013 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/3.0/>. The written permission of Cambridge University Press must be obtained for commercial re-use.
spellingShingle Original Articles
Rocha-Rego, V.
Jogia, J.
Marquand, A. F.
Mourao-Miranda, J.
Simmons, A.
Frangou, S.
Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title_full Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title_fullStr Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title_full_unstemmed Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title_short Examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
title_sort examination of the predictive value of structural magnetic resonance scans in bipolar disorder: a pattern classification approach
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880067/
https://www.ncbi.nlm.nih.gov/pubmed/23734914
http://dx.doi.org/10.1017/S0033291713001013
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