Striatal gray matter loss in Huntington's disease is leftward biased
Identifieur interne : 002B57 ( Main/Exploration ); précédent : 002B56; suivant : 002B58Striatal gray matter loss in Huntington's disease is leftward biased
Auteurs : Mark Mühlau [Allemagne] ; Christian Gaser [Allemagne] ; Afra M. Wohlschl Ger [Allemagne] ; Adolf Weindl [Allemagne] ; Michael St Dtler [Allemagne] ; Michael Valet [Allemagne] ; Claus Zimmer [Allemagne] ; Jan Kassubek [Allemagne] ; Alexander Peinemann [Allemagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-06-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Adult, Aged, Brain (pathology), Cognition Disorders (diagnosis), Cognition Disorders (epidemiology), Corpus Striatum (pathology), Female, Functional Laterality (physiology), Humans, Huntington Disease (diagnosis), Huntington Disease (epidemiology), Huntington Disease (pathology), Huntington disease, Huntington's disease, Male, Middle Aged, Morphometry, Nerve Degeneration (epidemiology), Nerve Degeneration (pathology), Nervous system diseases, Neuropsychological Tests, Severity of Illness Index, Voxel, gray matter loss, lateralization, striatum, voxel‐based morphometry.
- MESH :
- diagnosis : Cognition Disorders, Huntington Disease.
- epidemiology : Cognition Disorders, Huntington Disease, Nerve Degeneration.
- pathology : Brain, Corpus Striatum, Huntington Disease, Nerve Degeneration.
- physiology : Functional Laterality.
- Adult, Aged, Female, Humans, Male, Middle Aged, Neuropsychological Tests, Severity of Illness Index.
Abstract
In Huntington's disease (HD), the distribution of pathological changes throughout the brain is incompletely understood. Some studies have identified leftward‐biased lateralization, whereas others did not. We performed magnetic resonance imaging and a voxel‐based asymmetry analysis in 44 right‐handed HD gene carriers (presymptomatic, n = 5; stage I, n = 28; stage II, n = 11) and 44 right‐handed healthy controls. The group comparison revealed leftward‐biased gray matter loss in the striatum. Further analyses showed no indication of asymmetry in presymptomatic HD patients but an increase in asymmetry in the course of the HD stages under examination. Our study demonstrates and discusses leftward‐biased gray matter loss in HD. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21137
Affiliations:
- Allemagne
- Bade-Wurtemberg, Bavière, District de Haute-Bavière, District de Tübingen
- Munich, Ulm
- Université d'Ulm, Université technique de Munich
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Le document en format XML
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<term>Corpus Striatum (pathology)</term>
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<term>Functional Laterality (physiology)</term>
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<term>Nerve Degeneration</term>
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<front><div type="abstract" xml:lang="en">In Huntington's disease (HD), the distribution of pathological changes throughout the brain is incompletely understood. Some studies have identified leftward‐biased lateralization, whereas others did not. We performed magnetic resonance imaging and a voxel‐based asymmetry analysis in 44 right‐handed HD gene carriers (presymptomatic, n = 5; stage I, n = 28; stage II, n = 11) and 44 right‐handed healthy controls. The group comparison revealed leftward‐biased gray matter loss in the striatum. Further analyses showed no indication of asymmetry in presymptomatic HD patients but an increase in asymmetry in the course of the HD stages under examination. Our study demonstrates and discusses leftward‐biased gray matter loss in HD. © 2007 Movement Disorder Society</div>
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