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Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy
BACKGROUND: The relationship between cortical thickness (CThick) and sulcal depth (SDepth) changes across brain regions during development. Epilepsy youth have CThick and SDepth abnormalities and prevalent psychiatric disorders. AIMS: This study compared the CThick–SDepth relationship in children wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal College of Psychiatrists
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995587/ https://www.ncbi.nlm.nih.gov/pubmed/27703737 http://dx.doi.org/10.1192/bjpo.bp.115.001719 |
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author | Tosun, Duygu Siddarth, Prabha Levitt, Jennifer Caplan, Rochelle |
author_facet | Tosun, Duygu Siddarth, Prabha Levitt, Jennifer Caplan, Rochelle |
author_sort | Tosun, Duygu |
collection | PubMed |
description | BACKGROUND: The relationship between cortical thickness (CThick) and sulcal depth (SDepth) changes across brain regions during development. Epilepsy youth have CThick and SDepth abnormalities and prevalent psychiatric disorders. AIMS: This study compared the CThick–SDepth relationship in children with focal epilepsy with typically developing children (TDC) and the role played by seizure and psychopathology variables. METHOD: A surface-based, computational high-resolution three-dimesional (3D) magnetic resonance image analytic technique compared regional CThick–SDepth relationships in 42 participants with focal epilepsy and 46 TDC (6–16 years) imaged in a 1.5 Tesla scanner. Psychiatric interviews administered to each participant yielded psychiatric diagnoses. Parents provided seizure-related information. RESULTS: The TDC group alone demonstrated a significant negative medial fronto-orbital CThick–SDepth correlation. Focal epilepsy participants with but not without psychiatric diagnoses showed significant positive pre-central and post-central CThick–SDepth associations not found in TDC. Although the history of prolonged seizures was significantly associated with the post-central CThick–SDepth correlation, it was unrelated to the presence/absence of psychiatric diagnoses. CONCLUSIONS: Abnormal CThick–SDepth pre-central and post-central associations might be a psychopathology biomarker in paediatric focal epilepsy. DECLARATION INTEREST: None. COPYRIGHT AND USAGE: © 2015 The Royal College of Psychiatrists. This is an open access article distributed under the terms of the Creative Commons Non-Commercial, No Derivatives (CC BY-NC-ND) licence. |
format | Online Article Text |
id | pubmed-4995587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal College of Psychiatrists |
record_format | MEDLINE/PubMed |
spelling | pubmed-49955872016-10-04 Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy Tosun, Duygu Siddarth, Prabha Levitt, Jennifer Caplan, Rochelle BJPsych Open Paper BACKGROUND: The relationship between cortical thickness (CThick) and sulcal depth (SDepth) changes across brain regions during development. Epilepsy youth have CThick and SDepth abnormalities and prevalent psychiatric disorders. AIMS: This study compared the CThick–SDepth relationship in children with focal epilepsy with typically developing children (TDC) and the role played by seizure and psychopathology variables. METHOD: A surface-based, computational high-resolution three-dimesional (3D) magnetic resonance image analytic technique compared regional CThick–SDepth relationships in 42 participants with focal epilepsy and 46 TDC (6–16 years) imaged in a 1.5 Tesla scanner. Psychiatric interviews administered to each participant yielded psychiatric diagnoses. Parents provided seizure-related information. RESULTS: The TDC group alone demonstrated a significant negative medial fronto-orbital CThick–SDepth correlation. Focal epilepsy participants with but not without psychiatric diagnoses showed significant positive pre-central and post-central CThick–SDepth associations not found in TDC. Although the history of prolonged seizures was significantly associated with the post-central CThick–SDepth correlation, it was unrelated to the presence/absence of psychiatric diagnoses. CONCLUSIONS: Abnormal CThick–SDepth pre-central and post-central associations might be a psychopathology biomarker in paediatric focal epilepsy. DECLARATION INTEREST: None. COPYRIGHT AND USAGE: © 2015 The Royal College of Psychiatrists. This is an open access article distributed under the terms of the Creative Commons Non-Commercial, No Derivatives (CC BY-NC-ND) licence. The Royal College of Psychiatrists 2015-10-22 /pmc/articles/PMC4995587/ /pubmed/27703737 http://dx.doi.org/10.1192/bjpo.bp.115.001719 Text en © 2015 The Royal College of Psychiatrists http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article distributed under the terms of the Creative Commons Non-Commercial, No Derivatives (CC BY-NC-ND) licence (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Paper Tosun, Duygu Siddarth, Prabha Levitt, Jennifer Caplan, Rochelle Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title_full | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title_fullStr | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title_full_unstemmed | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title_short | Cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
title_sort | cortical thickness and sulcal depth: insights on development and psychopathology in paediatric epilepsy |
topic | Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995587/ https://www.ncbi.nlm.nih.gov/pubmed/27703737 http://dx.doi.org/10.1192/bjpo.bp.115.001719 |
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