Cerebellar voxel-based morphometry in essential tremor.


Journal

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

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 12 04 2022
accepted: 12 07 2022
revised: 29 06 2022
pubmed: 20 7 2022
medline: 14 10 2022
entrez: 19 7 2022
Statut: ppublish

Résumé

Imaging studies investigating cerebellar gray matter (GM) in essential tremor (ET) showed conflicting results. Moreover, no large study explored the cerebellum in ET patients with resting tremor (rET), a syndrome showing enhanced blink reflex recovery cycle (BRrc). To investigate cerebellar GM in ET and rET patients using voxel-based morphometry (VBM) analysis. Seventy ET patients with or without resting tremor and 39 healthy controls were enrolled. All subjects underwent brain 3 T-MRI and BRrc recording. We compared the cerebellar GM volumes between ET (n = 40) and rET (n = 30) patients and controls through a VBM analysis. Moreover, we investigated possible correlations between cerebellar GM volume and R2 component of BRrc. rET and ET patients had similar disease duration. All rET patients and none of ET patients had enhanced BRrc. No differences in the cerebellar volume were found when ET and rET patients were compared to each other or with controls. By considering together the two tremor syndromes in a large patient group, the VBM analysis showed bilateral clusters of reduced GM volumes in Crus II in comparison with controls. The linear regression analysis in rET patients revealed a cluster in the left Crus II where the decrease in GM volume correlated with the R2BRrc increase. Our study suggests that ET and rET are different tremor syndromes with similar mild cerebellar gray matter involvement. In rET patients, the left Crus II may play a role in modulating the brainstem excitability, encouraging further studies on the role of cerebellum in these patients.

Sections du résumé

BACKGROUND BACKGROUND
Imaging studies investigating cerebellar gray matter (GM) in essential tremor (ET) showed conflicting results. Moreover, no large study explored the cerebellum in ET patients with resting tremor (rET), a syndrome showing enhanced blink reflex recovery cycle (BRrc).
OBJECTIVE OBJECTIVE
To investigate cerebellar GM in ET and rET patients using voxel-based morphometry (VBM) analysis.
METHODS METHODS
Seventy ET patients with or without resting tremor and 39 healthy controls were enrolled. All subjects underwent brain 3 T-MRI and BRrc recording. We compared the cerebellar GM volumes between ET (n = 40) and rET (n = 30) patients and controls through a VBM analysis. Moreover, we investigated possible correlations between cerebellar GM volume and R2 component of BRrc.
RESULTS RESULTS
rET and ET patients had similar disease duration. All rET patients and none of ET patients had enhanced BRrc. No differences in the cerebellar volume were found when ET and rET patients were compared to each other or with controls. By considering together the two tremor syndromes in a large patient group, the VBM analysis showed bilateral clusters of reduced GM volumes in Crus II in comparison with controls. The linear regression analysis in rET patients revealed a cluster in the left Crus II where the decrease in GM volume correlated with the R2BRrc increase.
CONCLUSION CONCLUSIONS
Our study suggests that ET and rET are different tremor syndromes with similar mild cerebellar gray matter involvement. In rET patients, the left Crus II may play a role in modulating the brainstem excitability, encouraging further studies on the role of cerebellum in these patients.

Identifiants

pubmed: 35852601
doi: 10.1007/s00415-022-11291-9
pii: 10.1007/s00415-022-11291-9
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6029-6035

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

Références

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Auteurs

Alessia Sarica (A)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Andrea Quattrone (A)

Institute of Neurology, Department of Medical and Surgical Sciences, Magna Graecia University, 88100, Catanzaro, Italy.

Marianna Crasà (M)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Rita Nisticò (R)

Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, 88100, Catanzaro, Italy.

Maria Grazia Vaccaro (MG)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Maria Giovanna Bianco (MG)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Vera Gramigna (V)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Marida De Maria (M)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy.

Basilio Vescio (B)

Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, 88100, Catanzaro, Italy.

Federico Rocca (F)

Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, 88100, Catanzaro, Italy.

Aldo Quattrone (A)

Department of Medical and Surgical Sciences, Neuroscience Research Center, Magna Graecia University, viale Europa, Germaneto, 88100, Catanzaro, Italy. quattrone@unicz.it.
Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, 88100, Catanzaro, Italy. quattrone@unicz.it.

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