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Semi-quantitative Assessment Using [18F]FDG Tracer in Patients with Severe Brain Injury
Published on: November 9, 2018
Semiquantitative analysis of cerebral [18F]FDG-PET uptake in pediatric patients
Álvaro Cruz-Cortes1, Arturo Avendaño-Estrada2, Sarael Alcauter3
1Unidad de Radiofarmacia-Ciclotrón, División de Investigación, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de Mexico, Mexico.
Insights
Brain glucose metabolism in children, measured by fluorodeoxyglucose-positron emission tomography (FDG-PET), changes with age and sex. Uptake increases until adolescence, with regional and sex differences observed.
Area of Science:
- Neuroscience
- Medical Imaging
- Pediatric Metabolism
Background:
- Brain glycolytic metabolism in pediatric patients using [18F]fluorodeoxyglucose-positron emission tomography (FDG-PET) is not fully understood.
- Characterizing normal brain FDG uptake is crucial for interpreting potential disease-related changes.
Purpose of the Study:
- To characterize [18F]FDG-PET brain uptake in a large cohort of pediatric patients without central nervous system diseases.
- To establish normative data for brain FDG uptake across different pediatric age groups.
Main Methods:
- Analysis of 795 [18F]FDG-PET scans from children under 18 years old without CNS diseases.
- Spatial normalization of brain images and calculation of standardized uptake values (SUV).
- Exploration of SUV as a function of age, sex, and brain region.
Main Results:
- Highest [18F]FDG uptake observed in the occipital lobe, lowest in the parietal lobe and brainstem.
- Brain FDG uptake increased with age until 12 years, with no significant changes from 13-17 years.
- Sex differences in whole-brain uptake were noted during adolescence, and hemispheric asymmetries were found in temporal and central regions during infancy.
Conclusions:
- Pediatric brain glycolytic metabolism, assessed by [18F]FDG-PET SUVmean, matures until early adolescence (under 13 years), with regional variations.
- Age, sex, and brain region significantly influence [18F]FDG uptake.
- Significant hemispheric asymmetries in temporal and central regions are present in infants.
Background:
Glycolytic metabolism in the brain of pediatric patients, imaged with [18F] fluorodeoxyglucose-positron emission tomography (FDG-PET) is incompletely characterized.
Objective:
The purpose of the current study was to characterize [18F]FDG-PET brain uptake in a large sample of pediatric patients with non-central nervous system diseases as an alternative to healthy subjects to evaluate changes at different pediatric ages.
Materials And Methods:
Seven hundred ninety-five [18F]FDG-PET examinations from children < 18 years of age without central nervous system diseases were included. Each brain image was spatially normalized, and the standardized uptake value (SUV) was obtained. The SUV and the SUV relative to different pseudo-references were explored as a function of age.
Results:
At all evaluated ages, the occipital lobe showed the highest [18F]FDG uptake (0.27 ± 0.04 SUV/year), while the parietal lobe and brainstem had the lowest uptake (0.17 ± 0.02 SUV/year, for both regions). An increase [18F]FDG uptake was found for all brain regions until 12 years old, while no significant uptake differences were found between ages 13 (SUV = 5.39) to 17 years old (SUV = 5.52) (P < 0.0001 for the whole brain). A sex dependence was found in the SUVmean for the whole brain during adolescence (SUV 5.04-5.25 for males, 5.68-5.74 for females, P = 0.0264). Asymmetries in [18F]FDG uptake were found in the temporal and central regions during infancy.
Conclusions:
Brain glycolytic metabolism of [18F]FDG, measured through the SUVmean, increased with age until early adolescence (< 13 years old), showing differences across brain regions. Age, sex, and brain region influence [18F]FDG uptake, with significant hemispheric asymmetries for temporal and central regions.
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