Multimodal characterization of the visual network in Huntington's disease gene carriers.


Journal

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319

Informations de publication

Date de publication:
11 2019
Historique:
received: 11 06 2019
revised: 25 07 2019
accepted: 12 08 2019
pubmed: 22 9 2019
medline: 9 6 2020
entrez: 22 9 2019
Statut: ppublish

Résumé

A sensorimotor network structural phenotype predicted motor task performance in a previous study in Huntington's disease (HD) gene carriers. We investigated in the visual network whether structure - function - behaviour relationship patterns, and the effects of the HD mutation, extended beyond the sensorimotor network. We used multimodal visual network MRI structural measures (cortical thickness and white matter connectivity), plus visual evoked potentials and task performance (Map Search; Symbol Digit Modalities Test) in healthy controls and HD gene carriers. Using principal component (PC) analysis, we identified a structure - function relationship common to both groups. PC scores differed between groups indicating white matter disorganization (higher RD, lower FA) and slower, and more disperse, VEP signal transmission (higher VEP P100 latency and lower VEP P100 amplitude) in HD than controls while task performance was similar. HD may be associated with reduced white matter organization and efficient visual network function but normal task performance. These findings indicate that structure - function relationships in the visual network, and the effects of the HD mutation, share some commonalities with those in the sensorimotor network. However, implications for task performance differ between the two networks suggesting the influence of network specific factors.

Identifiants

pubmed: 31541982
pii: S1388-2457(19)31204-0
doi: 10.1016/j.clinph.2019.08.018
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2053-2059

Subventions

Organisme : Wellcome Trust
ID : 200181/Z/15/Z
Pays : United Kingdom

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Sarah Gregory (S)

Huntington's Disease Centre, UCL Institute of Neurology, London, UK.

Omar F F Odish (OFF)

Department of Neurology, University Medical Center Groningen, Groningen, the Netherlands.

Isabella Mayer (I)

Department of Neurology, Ulm University Hospital, Ulm, Germany.

James Mills (J)

Department of Psychiatry, University of Iowa, Iowa City, IA, USA.

Eileanoir B Johnson (EB)

Huntington's Disease Centre, UCL Institute of Neurology, London, UK.

Rachael I Scahill (RI)

Huntington's Disease Centre, UCL Institute of Neurology, London, UK.

John Rothwell (J)

Sobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, Queen Square, London, UK.

Geraint Rees (G)

Wellcome Trust Centre for Neuroimaging, University College London, London, UK.

Jeffrey D Long (JD)

Department of Psychiatry, University of Iowa, Iowa City, IA, USA; Department of Biostatistics, University of Iowa, Iowa City, IA, USA.

Sarah J Tabrizi (SJ)

Huntington's Disease Centre, UCL Institute of Neurology, London, UK.

Raymund A C Roos (RAC)

Department of Neurology, Leiden University Medical Centre, Leiden, the Netherlands.

Michael Orth (M)

Department of Neurology, Ulm University Hospital, Ulm, Germany. Electronic address: michael.orth@uni-ulm.de.

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