La maladie de Parkinson au Canada (serveur d'exploration)

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Network structure of brain atrophy in de novo Parkinson's disease

Identifieur interne : 000356 ( France/Analysis ); précédent : 000355; suivant : 000357

Network structure of brain atrophy in de novo Parkinson's disease

Auteurs : Yashar Zeighami [Canada] ; Miguel Ulla [Canada, France] ; Yasser Iturria-Medina [Canada] ; Mahsa Dadar [Canada] ; Yu Zhang [Canada] ; Kevin Michel-Herve Larcher [Canada] ; Vladimir Fonov [Canada] ; Alan C. Evans [Canada] ; D Louis Collins [Canada] ; Alain Dagher [Canada]

Source :

RBID : PMC:4596689

English descriptors

Abstract

We mapped the distribution of atrophy in Parkinson's disease (PD) using magnetic resonance imaging (MRI) and clinical data from 232 PD patients and 117 controls from the Parkinson's Progression Markers Initiative. Deformation-based morphometry and independent component analysis identified PD-specific atrophy in the midbrain, basal ganglia, basal forebrain, medial temporal lobe, and discrete cortical regions. The degree of atrophy reflected clinical measures of disease severity. The spatial pattern of atrophy demonstrated overlap with intrinsic networks present in healthy brain, as derived from functional MRI. Moreover, the degree of atrophy in each brain region reflected its functional and anatomical proximity to a presumed disease epicenter in the substantia nigra, compatible with a trans-neuronal spread of the disease. These results support a network-spread mechanism in PD. Finally, the atrophy pattern in PD was also seen in healthy aging, where it also correlated with the loss of striatal dopaminergic innervation.

DOI:http://dx.doi.org/10.7554/eLife.08440.001


Url:
DOI: 10.7554/eLife.08440
PubMed: 26344547
PubMed Central: 4596689


Affiliations:


Links toward previous steps (curation, corpus...)


Links to Exploration step

PMC:4596689

Le document en format XML

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<p>We mapped the distribution of atrophy in Parkinson's disease (PD) using magnetic resonance imaging (MRI) and clinical data from 232 PD patients and 117 controls from the Parkinson's Progression Markers Initiative. Deformation-based morphometry and independent component analysis identified PD-specific atrophy in the midbrain, basal ganglia, basal forebrain, medial temporal lobe, and discrete cortical regions. The degree of atrophy reflected clinical measures of disease severity. The spatial pattern of atrophy demonstrated overlap with intrinsic networks present in healthy brain, as derived from functional MRI. Moreover, the degree of atrophy in each brain region reflected its functional and anatomical proximity to a presumed disease epicenter in the substantia nigra, compatible with a trans-neuronal spread of the disease. These results support a network-spread mechanism in PD. Finally, the atrophy pattern in PD was also seen in healthy aging, where it also correlated with the loss of striatal dopaminergic innervation.</p>
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<bold>DOI:</bold>
<ext-link ext-link-type="doi" xlink:href="10.7554/eLife.08440.001">http://dx.doi.org/10.7554/eLife.08440.001</ext-link>
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