Modulation of metabolic brain networks after subthalamic gene therapy for Parkinson's disease. Academic Article uri icon

Overview

abstract

  • Parkinson's disease (PD) is characterized by elevated expression of an abnormal metabolic brain network that is reduced by clinically effective treatment. We used fluorodeoxyglucose (FDG) positron emission tomography (PET) to determine the basis for motor improvement in 12 PD patients receiving unilateral subthalamic nucleus (STN) infusion of an adenoassociated virus vector expressing glutamic acid decarboxylase (AAV-GAD). After gene therapy, we observed significant reductions in thalamic metabolism on the operated side as well as concurrent metabolic increases in ipsilateral motor and premotor cortical regions. Abnormal elevations in the activity of metabolic networks associated with motor and cognitive functioning in PD patients were evident at baseline. The activity of the motor-related network declined after surgery and persisted at 1 year. These network changes correlated with improved clinical disability ratings. By contrast, the activity of the cognition-related network did not change after gene transfer. This suggests that modulation of abnormal network activity underlies the clinical outcome observed after unilateral STN AAV-GAD gene therapy. Network biomarkers may be used as physiological assays in early-phase trials of experimental therapies for PD and other neurodegenerative disease.

publication date

  • November 27, 2007

Research

keywords

  • Brain
  • Genetic Therapy
  • Glutamate Decarboxylase
  • Parkinson Disease

Identity

PubMed Central ID

  • PMC2148328

Scopus Document Identifier

  • 37349011012

Digital Object Identifier (DOI)

  • 10.1073/pnas.0706006104

PubMed ID

  • 18042721

Additional Document Info

volume

  • 104

issue

  • 49