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Neuroanatomical profiles of personality change in frontotemporal lobar degeneration
Background The neurobiological basis of personality is poorly understood. Frontotemporal lobar degeneration (FTLD) frequently presents with complex behavioural changes, and therefore potentially provides a disease model in which to investigate brain substrates of personality. Aims To assess neuroana...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Royal College Of Psychiatrists
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3093679/ https://www.ncbi.nlm.nih.gov/pubmed/21372059 http://dx.doi.org/10.1192/bjp.bp.110.082677 |
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author | Mahoney, Colin J. Rohrer, Jonathan D. Omar, Rohani Rossor, Martin N. Warren, Jason D. |
author_facet | Mahoney, Colin J. Rohrer, Jonathan D. Omar, Rohani Rossor, Martin N. Warren, Jason D. |
author_sort | Mahoney, Colin J. |
collection | PubMed |
description | Background The neurobiological basis of personality is poorly understood. Frontotemporal lobar degeneration (FTLD) frequently presents with complex behavioural changes, and therefore potentially provides a disease model in which to investigate brain substrates of personality. Aims To assess neuroanatomical correlates of personality change in a cohort of individuals with FTLD using voxel-based morphometry (VBM). Method Thirty consecutive individuals fulfilling consensus criteria for FTLD were assessed. Each participant’s carer completed a Big Five Inventory (BFI) questionnaire on five key personality traits; for each trait, a change score was derived based on current compared with estimated premorbid characteristics. All participants underwent volumetric brain magnetic resonance imaging. A VBM analysis was implemented regressing change score for each trait against regional grey matter volume across the FTLD group. Results The FTLD group showed a significant decline in extraversion, agreeableness, conscientiousness and openness and an increase in neuroticism. Change in particular personality traits was associated with overlapping profiles of grey matter loss in more anterior cortical areas and relative preservation of grey matter in more posterior areas; the most robust neuroanatomical correlate was identified for reduced conscientiousness in the region of the posterior superior temporal gyrus. Conclusions Quantitative measures of personality change in FTLD can be correlated with changes in regional grey matter. The neuroanatomical profiles for particular personality traits overlap brain circuits previously implicated in aspects of social cognition and suggest that dysfunction at the level of distributed cortical networks underpins personality change in FTLD. |
format | Text |
id | pubmed-3093679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Royal College Of Psychiatrists |
record_format | MEDLINE/PubMed |
spelling | pubmed-30936792011-06-15 Neuroanatomical profiles of personality change in frontotemporal lobar degeneration Mahoney, Colin J. Rohrer, Jonathan D. Omar, Rohani Rossor, Martin N. Warren, Jason D. Br J Psychiatry Papers Background The neurobiological basis of personality is poorly understood. Frontotemporal lobar degeneration (FTLD) frequently presents with complex behavioural changes, and therefore potentially provides a disease model in which to investigate brain substrates of personality. Aims To assess neuroanatomical correlates of personality change in a cohort of individuals with FTLD using voxel-based morphometry (VBM). Method Thirty consecutive individuals fulfilling consensus criteria for FTLD were assessed. Each participant’s carer completed a Big Five Inventory (BFI) questionnaire on five key personality traits; for each trait, a change score was derived based on current compared with estimated premorbid characteristics. All participants underwent volumetric brain magnetic resonance imaging. A VBM analysis was implemented regressing change score for each trait against regional grey matter volume across the FTLD group. Results The FTLD group showed a significant decline in extraversion, agreeableness, conscientiousness and openness and an increase in neuroticism. Change in particular personality traits was associated with overlapping profiles of grey matter loss in more anterior cortical areas and relative preservation of grey matter in more posterior areas; the most robust neuroanatomical correlate was identified for reduced conscientiousness in the region of the posterior superior temporal gyrus. Conclusions Quantitative measures of personality change in FTLD can be correlated with changes in regional grey matter. The neuroanatomical profiles for particular personality traits overlap brain circuits previously implicated in aspects of social cognition and suggest that dysfunction at the level of distributed cortical networks underpins personality change in FTLD. Royal College Of Psychiatrists 2011-05 /pmc/articles/PMC3093679/ /pubmed/21372059 http://dx.doi.org/10.1192/bjp.bp.110.082677 Text en Copyright © 2011, Royal College of Psychiatrists This paper accords with the Wellcome Trust Open Access policy and is governed by the licence available at http://www.rcpsych.ac.uk/pdf/Wellcome%20Trust%20licence.pdf |
spellingShingle | Papers Mahoney, Colin J. Rohrer, Jonathan D. Omar, Rohani Rossor, Martin N. Warren, Jason D. Neuroanatomical profiles of personality change in frontotemporal lobar degeneration |
title | Neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
title_full | Neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
title_fullStr | Neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
title_full_unstemmed | Neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
title_short | Neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
title_sort | neuroanatomical profiles of personality change in frontotemporal
lobar degeneration |
topic | Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3093679/ https://www.ncbi.nlm.nih.gov/pubmed/21372059 http://dx.doi.org/10.1192/bjp.bp.110.082677 |
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