Abnormal metabolic brain networks in Parkinson's disease: from blackboard to bedside

被引:22
作者
Bjorklund, Anders [1 ]
Cenci, M. Angela [2 ]
机构
[1] Lund Univ, Div Neurobiol, Wallenberg Neurosci Ctr, Lund, Sweden
[2] Lund Univ, Dept Expt Med Sci, Basal Ganglia Pathophysiol Unit, Lund, Sweden
来源
RECENT ADVANCES IN PARKINSONS DISEASE: TRANSLATIONAL AND CLINICAL RESEARCH | 2010年 / 184卷
关键词
brain networks; glucose metabolism; Parkinson's disease; differential diagnosis; SLEEP BEHAVIOR DISORDER; GENE-THERAPY; CLINICAL-DIAGNOSIS; SUBTHALAMIC NUCLEUS; DIFFERENTIAL-DIAGNOSIS; ATYPICAL PARKINSONISM; ALZHEIMERS-DISEASE; ESSENTIAL TREMOR; GAD GENE; FDG-PET;
D O I
10.1016/S0079-6123(10)84008-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Metabolic imaging in the rest state has provided valuable information concerning the abnormalities of regional brain function that underlie idiopathic Parkinson's disease (PD). Moreover, network modeling procedures, such as spatial covariance analysis, have further allowed for the quantification of these changes at the systems level. In recent years, we have utilized this strategy to identify and validate three discrete metabolic networks in PD associated with the motor and cognitive manifestations of the disease. In this chapter, we will review and compare the specific functional topographies underlying parkinsonian akinesia/rigidity, tremor, and cognitive disturbance. While network activity progressed over time, the rate of change for each pattern was distinctive and paralleled the development of the corresponding clinical symptoms in early-stage patients. This approach is already showing great promise in identifying individuals with prodromal manifestations of PD and in assessing the rate of progression before clinical onset. Network modulation was found to correlate with the clinical effects of dopaminergic treatment and surgical interventions, such as subthalamic nucleus (STN) deep brain stimulation (DBS) and gene therapy. Abnormal metabolic networks have also been identified for atypical parkinsonian syndromes, such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). Using multiple disease-related networks for PD, MSA, and PSP, we have developed a novel, fully automated algorithm for accurate classification at the single-patient level, even at early disease stages.
引用
收藏
页码:161 / 176
页数:16
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