4.6 Article

Abnormal metabolic network activity in Parkinson's disease: test-retest reproducibility

Journal

JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
Volume 27, Issue 3, Pages 597-605

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.jcbfm.9600358

Keywords

cerebral blood flow; glucose metabolism; PCA; PD; test-retest reliability

Funding

  1. NCRR NIH HHS [M01 RR 018535, M01 RR018535-056239, M01 RR018535] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS035069-08, R01 NS035069, R01 NS 35069] Funding Source: Medline

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Parkinson's disease ( PD) is associated with an abnormal pattern of regional brain function. The expression of this PD- related covariance pattern ( PDRP) has been used to assess disease progression and the response to treatment. In this study, we validated the PDRP network as a measure of parkinsonism by prospectively computing its expression ( PDRP scores) in O-15- water ((H2O)-O-15) and F-18- fluorodeoxyglucose ( FDG) positron emission tomography ( PET) scans from PD patients and healthy volunteers. The reliability of this measure was also assessed within subjects using a test - retest design in mildly affected and advanced PD patients scanned at baseline and during treatment with levodopa or deep brain stimulation ( DBS). We found that PDRP expression was significantly elevated in PD patients ( P < 0.001) relative to controls in a prospective analysis of brain scans obtained with either (H2O)-O-15 or FDG PET. A significant correlation ( R-2 = 0.61; P < 0.001) was evident between PDRP scores computed from (H2O)-O-15 and FDG images in PD subjects scanned with both tracers. Test - retest reproducibility was very high ( intraclass correlation coefficient ( ICC) > 0.92) for PDRP scores measured both within PET session and between sessions separated by up to 2 months. This high reproducibility was observed in both early stage and advanced PD patients scanned at baseline and during treatment. The within- subject variability of this measure was less than 10% for both unmedicated and treated conditions. These findings suggest that the PDRP network is a reproducible and stable descriptor of regional functional abnormalities in parkinsonism. The quantification of PDRP expression in PD patients can serve as a potential biomarker in PET intervention studies for this disorder.

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