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Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)

OBJECTIVE: Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a rare neurodegenerative disease for which there is no specific treatment. Very few cases have been treated with single-target deep brain stimulation (DBS), and the results were not satisfactory. We appli...

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Autores principales: Cui, Zhiqiang, Lan, Yina, Chang, Yan, Liu, Xinyun, Wang, Jian, Lou, Xin, Wang, Ruimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564991/
https://www.ncbi.nlm.nih.gov/pubmed/37830087
http://dx.doi.org/10.3389/fneur.2023.1246430
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author Cui, Zhiqiang
Lan, Yina
Chang, Yan
Liu, Xinyun
Wang, Jian
Lou, Xin
Wang, Ruimin
author_facet Cui, Zhiqiang
Lan, Yina
Chang, Yan
Liu, Xinyun
Wang, Jian
Lou, Xin
Wang, Ruimin
author_sort Cui, Zhiqiang
collection PubMed
description OBJECTIVE: Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a rare neurodegenerative disease for which there is no specific treatment. Very few cases have been treated with single-target deep brain stimulation (DBS), and the results were not satisfactory. We applied multi-target DBS to an SCA3/MJD patient and performed positron emission computed tomography (PET) before and after DBS to explore the short-term clinical therapeutic effect. MATERIALS AND METHODS: A 26-year-old right-hand-dominant female with a family history of SCA3/MJD suffered from cerebellar ataxia and dystonia. Genetic testing indicated an expanded CAG trinucleotide repeat in the ATXN3 gene and a diagnosis of SCA3/MJD. Conservative treatment had no obvious effect; therefore, leads were implanted in the bilateral dentate nucleus (DN) and the globus pallidus internus (GPi) and connected to an external stimulation device. The treatment effect was evaluated in a double-blind, randomized protocol in five phases (over a total of 15 days): no stimulation, GPi, DN, or sham stimulation, and combined GPi and DN stimulation. (18)F-fluoro-2-deoxy-d-glucose and dopamine transporter PET, Scale for the Assessment and Rating of Ataxia, Fahn-Tolosa-Marin Clinical Rating Scale for Tremor (FTM), Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS), and SF-36 quality of life scores were compared before and after DBS. RESULTS: The Total Scale for the Assessment and Rating of Ataxia scores improved by ~42% (from 24 to 14). The BFMDRS movement scores improved by ~30% (from 40.5 to 28.5). The BFMDRS disability scores improved by ~12.5% (from 16 to 14). Daily living activities were not noticeably improved. Compared with the findings in pre-DBS imaging, (18)F-fluoro-2-deoxy-d-glucose uptake increased in the cerebellum, while according to dopamine transporter imaging, there were no significant differences in the bilateral caudate nucleus and putamen. CONCLUSION: Multi-target acute stimulation (DN DBS and GPi DBS) in SCA3/MJD can mildly improve cerebellar ataxia and dystonia and increase cerebellar metabolism.
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spelling pubmed-105649912023-10-12 Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD) Cui, Zhiqiang Lan, Yina Chang, Yan Liu, Xinyun Wang, Jian Lou, Xin Wang, Ruimin Front Neurol Neurology OBJECTIVE: Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a rare neurodegenerative disease for which there is no specific treatment. Very few cases have been treated with single-target deep brain stimulation (DBS), and the results were not satisfactory. We applied multi-target DBS to an SCA3/MJD patient and performed positron emission computed tomography (PET) before and after DBS to explore the short-term clinical therapeutic effect. MATERIALS AND METHODS: A 26-year-old right-hand-dominant female with a family history of SCA3/MJD suffered from cerebellar ataxia and dystonia. Genetic testing indicated an expanded CAG trinucleotide repeat in the ATXN3 gene and a diagnosis of SCA3/MJD. Conservative treatment had no obvious effect; therefore, leads were implanted in the bilateral dentate nucleus (DN) and the globus pallidus internus (GPi) and connected to an external stimulation device. The treatment effect was evaluated in a double-blind, randomized protocol in five phases (over a total of 15 days): no stimulation, GPi, DN, or sham stimulation, and combined GPi and DN stimulation. (18)F-fluoro-2-deoxy-d-glucose and dopamine transporter PET, Scale for the Assessment and Rating of Ataxia, Fahn-Tolosa-Marin Clinical Rating Scale for Tremor (FTM), Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS), and SF-36 quality of life scores were compared before and after DBS. RESULTS: The Total Scale for the Assessment and Rating of Ataxia scores improved by ~42% (from 24 to 14). The BFMDRS movement scores improved by ~30% (from 40.5 to 28.5). The BFMDRS disability scores improved by ~12.5% (from 16 to 14). Daily living activities were not noticeably improved. Compared with the findings in pre-DBS imaging, (18)F-fluoro-2-deoxy-d-glucose uptake increased in the cerebellum, while according to dopamine transporter imaging, there were no significant differences in the bilateral caudate nucleus and putamen. CONCLUSION: Multi-target acute stimulation (DN DBS and GPi DBS) in SCA3/MJD can mildly improve cerebellar ataxia and dystonia and increase cerebellar metabolism. Frontiers Media S.A. 2023-09-27 /pmc/articles/PMC10564991/ /pubmed/37830087 http://dx.doi.org/10.3389/fneur.2023.1246430 Text en Copyright © 2023 Cui, Lan, Chang, Liu, Wang, Lou and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Cui, Zhiqiang
Lan, Yina
Chang, Yan
Liu, Xinyun
Wang, Jian
Lou, Xin
Wang, Ruimin
Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title_full Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title_fullStr Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title_full_unstemmed Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title_short Case report: Short-term efficacy and changes in (18)F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD)
title_sort case report: short-term efficacy and changes in (18)f-fdg-pet with acute multi-target stimulation in spinocerebellar ataxia type 3 (sca3/mjd)
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564991/
https://www.ncbi.nlm.nih.gov/pubmed/37830087
http://dx.doi.org/10.3389/fneur.2023.1246430
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