4.6 Article

Metabolic Networks for Assessment of Therapy and Diagnosis in Parkinson's Disease

Journal

MOVEMENT DISORDERS
Volume 24, Issue 14, Pages S725-S731

Publisher

WILEY
DOI: 10.1002/mds.22541

Keywords

positron emission tomography; Parkinson's disease; brain metabolism; differential diagnosis; treatment response

Funding

  1. NIH NINDS [R01 35069, P50 NS 38370]
  2. NS-LIJ Health System [NIH RR M01 018535]
  3. Neurologix Inc.
  4. Parkinson's Disease Foundation
  5. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR018535] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS035069, P50NS038370] Funding Source: NIH RePORTER

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Neuroimaging and modern computational techniques like spatial covariance analysis have contributed greatly to the understanding of neural system abnormalities in neuro-degenerative disorders Such as Parkinson's disease (PD). The application of network analysis to metabolic PET data obtained from patients with PD has led to the identification and validation of two distinct spatial covariance patterns associated with the motor and cognitive manifestations of the disease. Quantifying the activity of these patterns in individual subjects has provided an objective tool for the assessment of treatment efficacy and differential diagnosis. We have found that activity of the PD motor-related network is modulated by antiparkinsonian treatments such as dopaminergic therapy, deep brain stimulation (DBS), and subthalamic nucleus (STN) gene therapy. By contrast, the cognitive-related network is not altered by these interventions for PD motor symptoms. This pattern may however change in response to therapies targeting the cognitive symptoms of this disorder. Recent work has focused on the identification of specific network biomarkers for atypical parkinsonian conditions such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). These disease-related patterns can potentially be used in an automated imaging-based algorithm to classify patients with these disorders. (c) 2009 Movement Disorder Society

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