Differentiating Parkinson's disease motor subtypes using automated volume-based morphometry incorporating white matter and deep gray nuclear lesion load.

Détails

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Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
ID Serval
serval:BIB_3A58877533DB
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Differentiating Parkinson's disease motor subtypes using automated volume-based morphometry incorporating white matter and deep gray nuclear lesion load.
Périodique
Journal of magnetic resonance imaging
Auteur⸱e⸱s
Fang E., Ann C.N., Maréchal B., Lim J.X., Tan SYZ, Li H., Gan J., Tan E.K., Chan L.L.
ISSN
1522-2586 (Electronic)
ISSN-L
1053-1807
Statut éditorial
Publié
Date de publication
03/2020
Peer-reviewed
Oui
Volume
51
Numéro
3
Pages
748-756
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Periventricular leukoaraiosis may be an important pathological change in postural instability gait disorder (PIGD), a motor subtype of Parkinson's disease (PD). Clinical diagnosis of PIGD may be challenging for the general neurologist.
To evaluate 1) the utility of a fully automated volume-based morphometry (Vol-BM) in characterizing imaging diagnostic markers in PD and PIGD, including, 2) novel deep gray nuclear lesion load (GMab), and 3) discriminatory performance of a Vol-BM model construct in classifying the PIGD subtype.
Prospective.
In all, 23 PIGD, 21 PD, and 20 age-matched healthy controls (HC) underwent MRI brain scans and clinical assessments.
3.0T, sagittal 3D-magnetization-prepared rapid gradient echo (MPRAGE), and fluid-attenuated inversion recovery imaging (FLAIR) sequences.
Clinical assessment was conducted by a movement disorder neurologist. The MR brain images were then segmented using an automated multimodal Vol-BM algorithm (MorphoBox) and reviewed by two authors independently.
Brain segmentation and clinical parameter differences and dependence were assessed using analysis of variance (ANOVA) and regression analysis, respectively. Logistic regression was performed to differentiate PIGD from PD, and discriminative reliability was evaluated using receiver operating characteristic (ROC) analysis.
Significantly higher white matter lesion load (WMab) (P < 0.01), caudate GMab (P < 0.05), and lateral and third ventricular (P < 0.05) volumetry were found in PIGD, compared with PD and HC. WMab, caudate and putamen GMab, and caudate, lateral, and third ventricular volumetry showed significant coefficients (P < 0.005) in linear regressions with balance and gait assessments in both patient groups. A model incorporating WMab, caudate GMab, and caudate GM discriminated PIGD from PD and HC with a sensitivity = 0.83 and specificity = 0.76 (AUC = 0.84).
Fast, unbiased quantification of microstructural brain changes in PD and PIGD is feasible using automated Vol-BM. Composite lesion load in the white matter and caudate, and caudate volumetry discriminated PIGD from PD and HC, and showed potential in classification of these disorders using supervised machine learning.
1 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2020;51:748-756.
Mots-clé
Parkinson's disease, abnormal deep gray matter, automated segmentation, postural instability gait disorder, volume-based morphometry
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/08/2019 9:36
Dernière modification de la notice
15/01/2021 8:08
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