Striatal dopamine function in a family with multiple SCA-3 phenotypes
- PMID: 20809346
- DOI: 10.1007/s00415-010-5724-z
Striatal dopamine function in a family with multiple SCA-3 phenotypes
Abstract
We present single photon emission computed tomography (SPECT) studies using 123IFP-CIT (DAT scan) and 123I-IBZM imaging, performed on four members of a family with genetically proven spinocerebellar ataxia type 3 (SCA-3). DAT scan showed significant asymmetric decreased binding in the striatum in the two members with predominant parkinsonian phenotype, with mild and symmetric decreased binding in the member with the cerebellar phenotype, and normal in the asymptomatic member. The IBZM SPECT studies showed mild and asymmetrical reduction of the striatal dopamine D2 receptor density (parkinsonian members). SCA-3 can present with a levodopa responsive parkinsonism phenotype, and an abnormal DAT scan showing predominant impairment of presynaptic dopamine function.
Similar articles
-
Diagnostic value of asymmetric striatal D2 receptor upregulation in Parkinson's disease: an [123I]IBZM and [123I]FP-CIT SPECT study.Eur J Nucl Med Mol Imaging. 2007 Apr;34(4):502-7. doi: 10.1007/s00259-006-0258-4. Epub 2006 Oct 20. Eur J Nucl Med Mol Imaging. 2007. PMID: 17053905
-
Dopamine transporter concentration is reduced in asymptomatic Machado-Joseph disease gene carriers.J Nucl Med. 2002 Feb;43(2):153-9. J Nucl Med. 2002. PMID: 11850478
-
FP-CIT- and IBZM-SPECT in Corticobasal Syndrome: Results from a Clinical Follow-Up Study.Neurodegener Dis. 2016;16(5-6):342-7. doi: 10.1159/000443667. Epub 2016 Mar 16. Neurodegener Dis. 2016. PMID: 26978429
-
The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family.Parkinsonism Relat Disord. 2004 Aug;10(6):369-73. doi: 10.1016/j.parkreldis.2004.03.009. Parkinsonism Relat Disord. 2004. PMID: 15261879
-
IBZM- and CIT-SPECT of the dopaminergic system in parkinsonism.J Neural Transm Suppl. 1997;50:31-7. doi: 10.1007/978-3-7091-6842-4_4. J Neural Transm Suppl. 1997. PMID: 9120422 Review.
Cited by
-
Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.Cerebellum Ataxias. 2016 Feb 23;3:4. doi: 10.1186/s40673-016-0042-6. eCollection 2016. Cerebellum Ataxias. 2016. PMID: 26909158 Free PMC article.
-
Spinocerebellar ataxia type 3: response to levodopa infusion in two cases.Neurol Sci. 2022 May;43(5):3423-3425. doi: 10.1007/s10072-022-05962-8. Epub 2022 Feb 24. Neurol Sci. 2022. PMID: 35199253
-
Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China.Mol Biol Rep. 2024 Jan 16;51(1):113. doi: 10.1007/s11033-023-09023-x. Mol Biol Rep. 2024. PMID: 38227102
-
Sleep Disorders in Hereditary Ataxias.Curr Neurol Neurosci Rep. 2019 Jul 25;19(8):59. doi: 10.1007/s11910-019-0968-1. Curr Neurol Neurosci Rep. 2019. PMID: 31342187 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources