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18[F]-FDG PET study on the Idiopathic Parkinson's disease from several parkinsonian-plus syndromes

✍ Scribed by Ping Zhao; Benshu Zhang; Shuo Gao


Book ID
117754392
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
517 KB
Volume
18
Category
Article
ISSN
1353-8020

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✦ Synopsis


Objective:

To investigate the difference in glucose metabolism on (18)f-fluorodeoxyglucose positron emission tomography ((18)f-fdg pet) imaging for differential diagnosis of idiopathic parkinson's disease (ipd) from several parkinsonian-plus syndromes using spm2 approach.

Methods:

(18)f-fdg pet was performed for 18 ipd patients, 22 multiple system atrophy (msa) patients, 13 progressive supranuclear palsy (psp) patients, 5 corticobasal degeneration (cbd) patients, 7 dementia with lewy bodies (dlb) patients and 1 normal pressure hydrocephalus (nph) patient. imaging-based diagnosis was obtained by statistical parametric mapping (spm2) software to analyze the differences and overlaps among these groups.

Results:

The (18)f-fdg pet images analyzed with spm2 demonstrated that a reduction in glucose metabolism occurred in bilateral parietal area for ipd, in bilateral putamen for msa-p, in bilateral cerebellum for msa-c, in midbrain and the middle frontal cortex for psp, in asymmetrical metabolism of the cortex and the basal ganglia for cbd, in bilateral occipital and parieto-occipital areas for dlb. the metabolic reductions in a patient of nph group were observed in the ventricular system.

Conclusions:

This study identifies different patterns of glucose metabolism in parkinsonism. (18)f-fdg pet imaging may contribute to early differential diagnosis in clinically ambiguous cases of parkinsonism.


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Comparison of brain MRI and 18F-FDG PET
✍ Kyum-Yil Kwon; Choong G. Choi; Jae S. Kim; Myoung C. Lee; Sun J. Chung πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 156 KB

## Abstract To investigate the diagnostic value of brain magnetic resonance image (MRI) and ^18^F‐fluorodeoxyglucose positron emission tomography (^18^F‐FDG PET) in the differentiation of multiple system atrophy (MSA) from Parkinson's disease (PD). Thirty‐five patients with MSA (23 MSA‐P and 12 MSA