Longitudinal clinical, cognitive, and neuroanatomical changes over 5 years in GBA-positive Parkinson's disease patients.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 14 04 2021
accepted: 11 07 2021
revised: 23 06 2021
pubmed: 24 7 2021
medline: 23 2 2022
entrez: 23 7 2021
Statut: ppublish

Résumé

To study the longitudinal disease course of Parkinson's disease (PD) patients with glucocerebrosidase (GBA) mutation (GBA-positive) compared to PD non-carriers (GBA-negative) along a 5-year follow-up, evaluating changes in clinical and cognitive outcomes, cortical thickness, and gray-matter (GM) volumes. Ten GBA-positive and 20 GBA-negative PD patients underwent clinical, neuropsychological, and MRI assessments (cortical thickness and subcortical, hippocampal, and amygdala volumes) at study entry and once a year for 5 years. At baseline and at the last visit, each group of patients was compared with 22 age-matched healthy controls. Clinical, cognitive, and MRI features were compared between groups at baseline and over time. At baseline, GBA-positive and GBA-negative PD patients had similar clinical and cognitive profiles. Compared to GBA-negative and controls, GBA-positive patients showed cortical thinning of left temporal, parietal, and occipital gyri. Over time, compared to GBA-negative, GBA-positive PD patients progressed significantly in motor and cognitive symptoms, and showed a greater pattern of cortical thinning of posterior regions, and frontal and orbito-frontal cortices. After 5 years, compared to controls, GBA-negative PD patients showed a pattern of cortical thinning similar to that showed by GBA-positive cases at baseline. The two groups of patients showed similar patterns of subcortical, hippocampal, and amygdala volume loss over time. Compared to GBA-negative PD, GBA-positive patients experienced a more rapid motor and cognitive decline together with a greater, earlier and faster cortical thinning. Cortical thickness measures may be a useful tool for monitoring and predicting PD progression in accordance with the genetic background.

Identifiants

pubmed: 34297177
doi: 10.1007/s00415-021-10713-4
pii: 10.1007/s00415-021-10713-4
doi:

Substances chimiques

Glucosylceramidase EC 3.2.1.45

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1485-1500

Subventions

Organisme : Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja
ID : #175090
Organisme : Ministero della Salute
ID : RF-2018-12366746

Informations de copyright

© 2021. Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Michela Leocadi (M)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Vita-Salute San Raffaele University, Via Olgettina, 60, 20132, Milan, Italy.

Elisa Canu (E)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.

Giulia Donzuso (G)

Section of Neurosciences, Department "G.F. Ingrassia", University of Catania, Catania, Italy.

Tanja Stojkovic (T)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Silvia Basaia (S)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.

Nikola Kresojević (N)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Iva Stankovic (I)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Elisabetta Sarasso (E)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.

Noemi Piramide (N)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Vita-Salute San Raffaele University, Via Olgettina, 60, 20132, Milan, Italy.

Aleksandra Tomic (A)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Vladana Markovic (V)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Igor Petrovic (I)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Elka Stefanova (E)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Vladimir S Kostic (VS)

Clinic of Neurology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Massimo Filippi (M)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Neurology Unit, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Neurophysiology Service, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Vita-Salute San Raffaele University, Via Olgettina, 60, 20132, Milan, Italy.

Federica Agosta (F)

Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy. agosta.federica@hsr.it.
Neurology Unit, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy. agosta.federica@hsr.it.
Vita-Salute San Raffaele University, Via Olgettina, 60, 20132, Milan, Italy. agosta.federica@hsr.it.

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