Ko Ji Hyun, Lee Chong Sik, Eidelberg David
1 Center for Neurosciences, The Feinstein Institute for Medical Research, Manhasset, NY, USA.
2 Department of Neurology, Asan Medical Center, Seoul, Republic of Korea.
J Cereb Blood Flow Metab. 2017 Feb;37(2):683-693. doi: 10.1177/0271678X16637880. Epub 2016 Jul 21.
Little is known of the precise relationship between the expression of disease-related metabolic patterns and nigrostriatal dopaminergic dysfunction in parkinsonism. We studied 51 subjects with Parkinson's disease (PD) (18 non-demented, 24 demented, and 9 dementia with Lewy bodies) and 127 with atypical parkinsonian syndromes (47 multiple system atrophy (MSA), 38 progressive supranuclear palsy (PSP), and 42 corticobasal syndrome (CBS)) with F-fluorodeoxyglucose PET to quantify the expression of previously validated disease-related patterns for PD, MSA, PSP, and CBS and F-fluoropropyl-β-CIT PET to quantify caudate and putamen dopamine transporter (DAT) binding. The patients in each group exhibited significant elevations in the expression of the corresponding disease-related pattern ( p < 0.001), relative to 16 healthy subjects. With the exception of cerebellar MSA (MSA-C), all groups displayed significant reductions in putamen DAT binding relative to healthy subjects ( p < 0.05). Correlations between the dopaminergic and metabolic measures were significant in PD and CBS but not in MSA and PSP. In all patient groups with the exception of MSA-C and CBS, pattern expression values and DAT binding correlated with disease duration and severity measures. The findings suggest that in these parkinsonian disorders, metabolic network expression and DAT binding provide complementary information regarding the underlying disease process.
关于帕金森病中疾病相关代谢模式的表达与黑质纹状体多巴胺能功能障碍之间的确切关系,目前所知甚少。我们对51例帕金森病(PD)患者(18例非痴呆患者、24例痴呆患者和9例路易体痴呆患者)以及127例非典型帕金森综合征患者(47例多系统萎缩(MSA)、38例进行性核上性麻痹(PSP)和42例皮质基底节综合征(CBS))进行了研究,采用F-氟脱氧葡萄糖PET来量化先前验证的PD、MSA、PSP和CBS疾病相关模式的表达,并采用F-氟丙基-β-CIT PET来量化尾状核和壳核多巴胺转运体(DAT)结合。与16名健康受试者相比,每组患者相应疾病相关模式的表达均显著升高(p < 0.001)。除小脑型MSA(MSA-C)外,所有组相对于健康受试者壳核DAT结合均显著降低(p < 0.05)。多巴胺能和代谢指标之间的相关性在PD和CBS中显著,但在MSA和PSP中不显著。除MSA-C和CBS外,所有患者组中,模式表达值和DAT结合与疾病持续时间和严重程度指标相关。这些发现表明,在这些帕金森病中,代谢网络表达和DAT结合为潜在疾病过程提供了互补信息。