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Early grey matter changes in structural covariance networks in Huntington's disease

BACKGROUND: Progressive subcortical changes are known to occur in Huntington's disease (HD), a hereditary neurodegenerative disorder. Less is known about the occurrence and cohesion of whole brain grey matter changes in HD. OBJECTIVES: We aimed to detect network integrity changes in grey matter...

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Autores principales: Coppen, Emma M., van der Grond, Jeroen, Hafkemeijer, Anne, Rombouts, Serge A.R.B., Roos, Raymund A.C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094265/
https://www.ncbi.nlm.nih.gov/pubmed/27830113
http://dx.doi.org/10.1016/j.nicl.2016.10.009
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author Coppen, Emma M.
van der Grond, Jeroen
Hafkemeijer, Anne
Rombouts, Serge A.R.B.
Roos, Raymund A.C
author_facet Coppen, Emma M.
van der Grond, Jeroen
Hafkemeijer, Anne
Rombouts, Serge A.R.B.
Roos, Raymund A.C
author_sort Coppen, Emma M.
collection PubMed
description BACKGROUND: Progressive subcortical changes are known to occur in Huntington's disease (HD), a hereditary neurodegenerative disorder. Less is known about the occurrence and cohesion of whole brain grey matter changes in HD. OBJECTIVES: We aimed to detect network integrity changes in grey matter structural covariance networks and examined relationships with clinical assessments. METHODS: Structural magnetic resonance imaging data of premanifest HD (n = 30), HD patients (n = 30) and controls (n = 30) was used to identify ten structural covariance networks based on a novel technique using the co-variation of grey matter with independent component analysis in FSL. Group differences were studied controlling for age and gender. To explore whether our approach is effective in examining grey matter changes, regional voxel-based analysis was additionally performed. RESULTS: Premanifest HD and HD patients showed decreased network integrity in two networks compared to controls. One network included the caudate nucleus, precuneous and anterior cingulate cortex (in HD p < 0.001, in pre-HD p = 0.003). One other network contained the hippocampus, premotor, sensorimotor, and insular cortices (in HD p < 0.001, in pre-HD p = 0.023). Additionally, in HD patients only, decreased network integrity was observed in a network including the lingual gyrus, intracalcarine, cuneal, and lateral occipital cortices (p = 0.032). Changes in network integrity were significantly associated with scores of motor and neuropsychological assessments. In premanifest HD, voxel-based analyses showed pronounced volume loss in the basal ganglia, but less prominent in cortical regions. CONCLUSION: Our results suggest that structural covariance might be a sensitive approach to reveal early grey matter changes, especially for premanifest HD.
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spelling pubmed-50942652016-11-09 Early grey matter changes in structural covariance networks in Huntington's disease Coppen, Emma M. van der Grond, Jeroen Hafkemeijer, Anne Rombouts, Serge A.R.B. Roos, Raymund A.C Neuroimage Clin Regular Article BACKGROUND: Progressive subcortical changes are known to occur in Huntington's disease (HD), a hereditary neurodegenerative disorder. Less is known about the occurrence and cohesion of whole brain grey matter changes in HD. OBJECTIVES: We aimed to detect network integrity changes in grey matter structural covariance networks and examined relationships with clinical assessments. METHODS: Structural magnetic resonance imaging data of premanifest HD (n = 30), HD patients (n = 30) and controls (n = 30) was used to identify ten structural covariance networks based on a novel technique using the co-variation of grey matter with independent component analysis in FSL. Group differences were studied controlling for age and gender. To explore whether our approach is effective in examining grey matter changes, regional voxel-based analysis was additionally performed. RESULTS: Premanifest HD and HD patients showed decreased network integrity in two networks compared to controls. One network included the caudate nucleus, precuneous and anterior cingulate cortex (in HD p < 0.001, in pre-HD p = 0.003). One other network contained the hippocampus, premotor, sensorimotor, and insular cortices (in HD p < 0.001, in pre-HD p = 0.023). Additionally, in HD patients only, decreased network integrity was observed in a network including the lingual gyrus, intracalcarine, cuneal, and lateral occipital cortices (p = 0.032). Changes in network integrity were significantly associated with scores of motor and neuropsychological assessments. In premanifest HD, voxel-based analyses showed pronounced volume loss in the basal ganglia, but less prominent in cortical regions. CONCLUSION: Our results suggest that structural covariance might be a sensitive approach to reveal early grey matter changes, especially for premanifest HD. Elsevier 2016-10-12 /pmc/articles/PMC5094265/ /pubmed/27830113 http://dx.doi.org/10.1016/j.nicl.2016.10.009 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Coppen, Emma M.
van der Grond, Jeroen
Hafkemeijer, Anne
Rombouts, Serge A.R.B.
Roos, Raymund A.C
Early grey matter changes in structural covariance networks in Huntington's disease
title Early grey matter changes in structural covariance networks in Huntington's disease
title_full Early grey matter changes in structural covariance networks in Huntington's disease
title_fullStr Early grey matter changes in structural covariance networks in Huntington's disease
title_full_unstemmed Early grey matter changes in structural covariance networks in Huntington's disease
title_short Early grey matter changes in structural covariance networks in Huntington's disease
title_sort early grey matter changes in structural covariance networks in huntington's disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094265/
https://www.ncbi.nlm.nih.gov/pubmed/27830113
http://dx.doi.org/10.1016/j.nicl.2016.10.009
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