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Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease

Disinhibition is an important symptom in neurodegenerative diseases. However, the clinico-anatomical underpinnings remain controversial. We explored the anatomical correlates of disinhibition in neurodegenerative disease using the perspective of grey and white matter imaging. Disinhibition was asses...

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Autores principales: Santillo, Alexander Frizell, Lundblad, Karl, Nilsson, Markus, Landqvist Waldö, Maria, van Westen, Danielle, Lätt, Jimmy, Blennow Nordström, Erik, Vestberg, Susanna, Lindberg, Olof, Nilsson, Christer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056728/
https://www.ncbi.nlm.nih.gov/pubmed/27723823
http://dx.doi.org/10.1371/journal.pone.0164122
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author Santillo, Alexander Frizell
Lundblad, Karl
Nilsson, Markus
Landqvist Waldö, Maria
van Westen, Danielle
Lätt, Jimmy
Blennow Nordström, Erik
Vestberg, Susanna
Lindberg, Olof
Nilsson, Christer
author_facet Santillo, Alexander Frizell
Lundblad, Karl
Nilsson, Markus
Landqvist Waldö, Maria
van Westen, Danielle
Lätt, Jimmy
Blennow Nordström, Erik
Vestberg, Susanna
Lindberg, Olof
Nilsson, Christer
author_sort Santillo, Alexander Frizell
collection PubMed
description Disinhibition is an important symptom in neurodegenerative diseases. However, the clinico-anatomical underpinnings remain controversial. We explored the anatomical correlates of disinhibition in neurodegenerative disease using the perspective of grey and white matter imaging. Disinhibition was assessed with a neuropsychological test and a caregiver information-based clinical rating scale in 21 patients with prefrontal syndromes due to behavioural variant frontotemporal dementia (n = 12) or progressive supranuclear palsy (n = 9), and healthy controls (n = 25). Cortical thickness was assessed using the Freesurfer software on 3T MRI data. The integrity of selected white matter tracts was determined by the fractional anisotropy (FA) from Diffusion Tensor Imaging. Disinhibition correlated with the cortical thickness of the right parahippocampal gyrus, right orbitofrontal cortex and right insula and the FA of the right uncinate fasciculus and right anterior cingulum. Notably, no relationship was seen with the thickness of ventromedial prefrontal cortex. Our results support an associative model of inhibitory control, distributed in a medial temporal lobe-insular-orbitofrontal network, connected by the intercommunicating white matter tracts. This reconciles some of the divergences among previous studies, but also questions the current conceptualisation of the “prefrontal” syndrome and the central role attributed to the ventromedial prefrontal cortex in inhibitory control.
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spelling pubmed-50567282016-10-27 Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease Santillo, Alexander Frizell Lundblad, Karl Nilsson, Markus Landqvist Waldö, Maria van Westen, Danielle Lätt, Jimmy Blennow Nordström, Erik Vestberg, Susanna Lindberg, Olof Nilsson, Christer PLoS One Research Article Disinhibition is an important symptom in neurodegenerative diseases. However, the clinico-anatomical underpinnings remain controversial. We explored the anatomical correlates of disinhibition in neurodegenerative disease using the perspective of grey and white matter imaging. Disinhibition was assessed with a neuropsychological test and a caregiver information-based clinical rating scale in 21 patients with prefrontal syndromes due to behavioural variant frontotemporal dementia (n = 12) or progressive supranuclear palsy (n = 9), and healthy controls (n = 25). Cortical thickness was assessed using the Freesurfer software on 3T MRI data. The integrity of selected white matter tracts was determined by the fractional anisotropy (FA) from Diffusion Tensor Imaging. Disinhibition correlated with the cortical thickness of the right parahippocampal gyrus, right orbitofrontal cortex and right insula and the FA of the right uncinate fasciculus and right anterior cingulum. Notably, no relationship was seen with the thickness of ventromedial prefrontal cortex. Our results support an associative model of inhibitory control, distributed in a medial temporal lobe-insular-orbitofrontal network, connected by the intercommunicating white matter tracts. This reconciles some of the divergences among previous studies, but also questions the current conceptualisation of the “prefrontal” syndrome and the central role attributed to the ventromedial prefrontal cortex in inhibitory control. Public Library of Science 2016-10-10 /pmc/articles/PMC5056728/ /pubmed/27723823 http://dx.doi.org/10.1371/journal.pone.0164122 Text en © 2016 Santillo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Santillo, Alexander Frizell
Lundblad, Karl
Nilsson, Markus
Landqvist Waldö, Maria
van Westen, Danielle
Lätt, Jimmy
Blennow Nordström, Erik
Vestberg, Susanna
Lindberg, Olof
Nilsson, Christer
Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title_full Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title_fullStr Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title_full_unstemmed Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title_short Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease
title_sort grey and white matter clinico-anatomical correlates of disinhibition in neurodegenerative disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056728/
https://www.ncbi.nlm.nih.gov/pubmed/27723823
http://dx.doi.org/10.1371/journal.pone.0164122
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