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White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder
Tourette syndrome (TS) and early-onset obsessive-compulsive disorder (OCD) are frequently associated and conceptualized as distinct phenotypes of a common disease spectrum. However, the nature of their relationship is still largely unknown on a pathophysiological level. In this study, early structur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575657/ https://www.ncbi.nlm.nih.gov/pubmed/36262836 http://dx.doi.org/10.3389/fneur.2022.960979 |
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author | Bharti, Komal Conte, Giulia Tommasin, Silvia Giannì, Costanza Suppa, Antonio Mirabella, Giovanni Cardona, Francesco Pantano, Patrizia |
author_facet | Bharti, Komal Conte, Giulia Tommasin, Silvia Giannì, Costanza Suppa, Antonio Mirabella, Giovanni Cardona, Francesco Pantano, Patrizia |
author_sort | Bharti, Komal |
collection | PubMed |
description | Tourette syndrome (TS) and early-onset obsessive-compulsive disorder (OCD) are frequently associated and conceptualized as distinct phenotypes of a common disease spectrum. However, the nature of their relationship is still largely unknown on a pathophysiological level. In this study, early structural white matter (WM) changes investigated through diffusion tensor imaging (DTI) were compared across four groups of drug-naïve children: TS-pure (n = 16), TS+OCD (n = 14), OCD (n = 10), and 11 age-matched controls. We analyzed five WM tracts of interest, i.e., cortico-spinal tract (CST), anterior thalamic radiations (ATR), inferior longitudinal fasciculus (ILF), corpus callosum (CC), and cingulum and evaluated correlations of DTI changes to symptom severity. Compared to controls, TS-pure and TS+OCD showed a comparable pattern of increased fractional anisotropy (FA) in CST, ATR, ILF and CC, with FA changes displaying negative correlation to tic severity. Conversely, in OCD, FA decreased in all WM tracts (except for the cingulum) compared to controls and negatively correlated to symptoms. We demonstrate different early WM microstructural alterations in children with TS-pure/TS+OCD as opposed to OCD. Our findings support the conceptualization of TS+OCD as a subtype of TS while suggesting that OCD is characterized by independent pathophysiological mechanisms affecting WM development. |
format | Online Article Text |
id | pubmed-9575657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95756572022-10-18 White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder Bharti, Komal Conte, Giulia Tommasin, Silvia Giannì, Costanza Suppa, Antonio Mirabella, Giovanni Cardona, Francesco Pantano, Patrizia Front Neurol Neurology Tourette syndrome (TS) and early-onset obsessive-compulsive disorder (OCD) are frequently associated and conceptualized as distinct phenotypes of a common disease spectrum. However, the nature of their relationship is still largely unknown on a pathophysiological level. In this study, early structural white matter (WM) changes investigated through diffusion tensor imaging (DTI) were compared across four groups of drug-naïve children: TS-pure (n = 16), TS+OCD (n = 14), OCD (n = 10), and 11 age-matched controls. We analyzed five WM tracts of interest, i.e., cortico-spinal tract (CST), anterior thalamic radiations (ATR), inferior longitudinal fasciculus (ILF), corpus callosum (CC), and cingulum and evaluated correlations of DTI changes to symptom severity. Compared to controls, TS-pure and TS+OCD showed a comparable pattern of increased fractional anisotropy (FA) in CST, ATR, ILF and CC, with FA changes displaying negative correlation to tic severity. Conversely, in OCD, FA decreased in all WM tracts (except for the cingulum) compared to controls and negatively correlated to symptoms. We demonstrate different early WM microstructural alterations in children with TS-pure/TS+OCD as opposed to OCD. Our findings support the conceptualization of TS+OCD as a subtype of TS while suggesting that OCD is characterized by independent pathophysiological mechanisms affecting WM development. Frontiers Media S.A. 2022-10-03 /pmc/articles/PMC9575657/ /pubmed/36262836 http://dx.doi.org/10.3389/fneur.2022.960979 Text en Copyright © 2022 Bharti, Conte, Tommasin, Giannì, Suppa, Mirabella, Cardona and Pantano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Bharti, Komal Conte, Giulia Tommasin, Silvia Giannì, Costanza Suppa, Antonio Mirabella, Giovanni Cardona, Francesco Pantano, Patrizia White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title | White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title_full | White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title_fullStr | White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title_full_unstemmed | White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title_short | White matter alterations in drug-naïve children with Tourette syndrome and obsessive-compulsive disorder |
title_sort | white matter alterations in drug-naïve children with tourette syndrome and obsessive-compulsive disorder |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575657/ https://www.ncbi.nlm.nih.gov/pubmed/36262836 http://dx.doi.org/10.3389/fneur.2022.960979 |
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