Striatal dopamine function in a family with multiple SCA-3 phenotypes

被引:11
作者
Cubo, Esther [1 ]
Diez Lopez, Mateo
Infante Ceberio, Jon [2 ,5 ]
Lanchas Alfonso, Isabel [6 ]
Miguel Martinez, Begona [6 ]
Berciano, Jose [2 ,5 ]
Iglesias, Fernando [1 ]
Obeso, Jose A. [3 ,4 ,5 ]
机构
[1] Hosp Gen Yague, Dept Neurol, Burgos 09005, Spain
[2] Univ Cantabria, Hosp Univ Marques de Valdecilla, Dept Neurol, E-39005 Santander, Spain
[3] Univ Navarra Clin, Dept Neurol, Navarra, Spain
[4] Univ Navarra, CIMA, Ctr Neurosci, Med Sch Navarra, Navarra, Spain
[5] Inst Salud Carlos III, Minist Invest & Ciencias, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid, Spain
[6] Hosp Divino Valles, Dept Nucl Med, Burgos, Spain
关键词
Dopamine; SCA-3; Parkinsonism; DAT scan; MACHADO-JOSEPH-DISEASE; GENE;
D O I
10.1007/s00415-010-5724-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:308 / 310
页数:3
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