Literature DB >> 26037537

Dopaminergic correlates of metabolic network activity in Parkinson's disease.

Florian Holtbernd1, Yilong Ma1, Shichun Peng1, Frank Schwartz2, Lars Timmermann2, Lutz Kracht3, Gereon R Fink2,4, Chris C Tang1, David Eidelberg1, Carsten Eggers2,3.   

Abstract

Parkinson's disease (PD) is associated with distinct metabolic covariance patterns that relate to the motor and cognitive manifestations of the disorder. It is not known, however, how the expression of these patterns relates to measurements of nigrostriatal dopaminergic activity from the same individuals. To explore these associations, we studied 106 PD subjects who underwent cerebral PET with both (18) F-fluorodeoxyglucose (FDG) and (18) F-fluoro-L-dopa (FDOPA). Expression values for the PD motor- and cognition-related metabolic patterns (PDRP and PDCP, respectively) were computed for each subject; these measures were correlated with FDOPA uptake on a voxel-by-voxel basis. To explore the relationship between dopaminergic function and local metabolic activity, caudate and putamen FDOPA PET signal was correlated voxel-wise with FDG uptake over the entire brain. PDRP expression correlated with FDOPA uptake in caudate and putamen (P < 0.001), while PDCP expression correlated with uptake in the anterior striatum (P < 0.001). While statistically significant, the correlations were only of modest size, accounting for less than 20% of the overall variation in these measures. After controlling for PDCP expression, PDRP correlations were significant only in the posterior putamen. Of note, voxel-wise correlations between caudate/putamen FDOPA uptake and whole-brain FDG uptake were significant almost exclusively in PDRP regions. Overall, the data indicate that PDRP and PDCP expression correlates significantly with PET indices of presynaptic dopaminergic functioning obtained in the same individuals. Even so, the modest size of these correlations suggests that in PD patients, individual differences in network activity cannot be explained solely by nigrostriatal dopamine loss.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  FDOPA; PET; Parkinson's disease; brain networks; dopamine

Mesh:

Substances:

Year:  2015        PMID: 26037537      PMCID: PMC6869564          DOI: 10.1002/hbm.22863

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


  39 in total

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5.  Striatal 18F-dopa uptake: absence of an aging effect.

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9.  Striatal FDOPA uptake and cognition in advanced non-demented Parkinson's disease: a clinical and FDOPA-PET study.

Authors:  Marije van Beilen; Axel T Portman; Henk A L Kiers; Ralph P Maguire; Valtteri Kaasinen; Marthe Koning; Jan Pruim; Klaus L Leenders
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3.  Dynamic brain glucose metabolism identifies anti-correlated cortical-cerebellar networks at rest.

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Review 7.  Recent Advancement and Clinical Implications of 18FDG-PET in Parkinson's Disease, Atypical Parkinsonisms, and Other Movement Disorders.

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8.  Flow-metabolism dissociation in the pathogenesis of levodopa-induced dyskinesia.

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Review 9.  New Imaging Markers for Movement Disorders.

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10.  Gray matter correlates of dopaminergic degeneration in Parkinson's disease: A hybrid PET/MR study using (18) F-FP-CIT.

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