Understanding the role of cerebellum in early Parkinson's disease: a structural and functional MRI study.


Journal

NPJ Parkinson's disease
ISSN: 2373-8057
Titre abrégé: NPJ Parkinsons Dis
Pays: United States
ID NLM: 101675390

Informations de publication

Date de publication:
19 Jun 2024
Historique:
received: 28 07 2023
accepted: 24 05 2024
medline: 20 6 2024
pubmed: 20 6 2024
entrez: 19 6 2024
Statut: epublish

Résumé

Increasing evidence suggests that the cerebellum may have a role in the pathophysiology of Parkinson's disease (PD). Hence, the scope of this study was to investigate whether there are structural and functional alterations of the cerebellum and whether they correlate with motor and non-motor symptoms in early PD patients. Seventy-six patients with early PD and thirty-one age and sex-matched healthy subjects (HS) were enrolled and underwent a 3 T magnetic resonance imaging (MRI) protocol. The following MRI analyses were performed: (1) volumes of 5 cerebellar regions of interest (sensorimotor and cognitive cerebellum, dentate, interposed, and fastigial nuclei); (2) microstructural integrity of the cerebellar white matter connections (inferior, middle, and superior cerebellar peduncles); (3) functional connectivity at rest of the 5 regions of interest already described in point 1 with the rest of brain. Compared to controls, early PD patients showed a significant decrease in gray matter volume of the dentate, interposed and fastigial nuclei, bilaterally. They also showed abnormal, bilateral white matter microstructural integrity in all 3 cerebellar peduncles. Functional connectivity of the 5 cerebellar regions of interest with several areas in the midbrain, basal ganglia and cerebral cortex was altered. Finally, there was a positive correlation between abnormal functional connectivity of the fastigial nucleus with the volume of the nucleus itself and a negative correlation with axial symptoms severity. Our results showed that structural and functional alterations of the cerebellum are present in PD patients and these changes contribute to the pathophysiology of PD in the early phase.

Identifiants

pubmed: 38898032
doi: 10.1038/s41531-024-00727-w
pii: 10.1038/s41531-024-00727-w
doi:

Types de publication

Journal Article

Langues

eng

Pagination

119

Informations de copyright

© 2024. The Author(s).

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Auteurs

S Pietracupa (S)

IRCCS Neuromed, Pozzilli, IS, Italy.
Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

A Ojha (A)

Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

D Belvisi (D)

IRCCS Neuromed, Pozzilli, IS, Italy.
Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

C Piervincenzi (C)

Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy. claudia.piervincenzi@uniroma1.it.

S Tommasin (S)

Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

N Petsas (N)

Department of Public Health and Infectious Disease, Sapienza University of Rome, Rome, Italy.

M I De Bartolo (MI)

IRCCS Neuromed, Pozzilli, IS, Italy.

M Costanzo (M)

IRCCS Neuromed, Pozzilli, IS, Italy.

A Fabbrini (A)

Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

A Conte (A)

IRCCS Neuromed, Pozzilli, IS, Italy.
Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

A Berardelli (A)

IRCCS Neuromed, Pozzilli, IS, Italy.
Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

P Pantano (P)

IRCCS Neuromed, Pozzilli, IS, Italy.
Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.

Classifications MeSH