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Published on: July 21, 2018
How Fluorine-18-labeled Fluorodeoxyglucose PET Changed Clinical Practice in Central Nervous System Disorders
Eric Guedj1, Andrew B Newberg2, Abass Alavi3
1Aix Marseille University, APHM, CNRS, Centrale Marseille, Institut Fresnel, Timone Hospital, CERIMED, Nuclear Medicine Department, Marseille, France.
None:
Over 5 decades, fluorine-18-labeled fluorodeoxyglucose ([18F]FDG) PET has transformed clinical practice in central nervous system (CNS) disorders by enabling in vivo assessment of brain metabolism as a surrogate of functional integrity. Beyond structural imaging, it provides reproducible, pattern-based biomarkers that improve diagnostic accuracy in dementia, epilepsy, and selected neuroinflammatory conditions. In the evolving biomarker landscape, [18F]FDG PET remains uniquely positioned to capture downstream network dysfunction and phenotypic expression of disease. Supported by standardized methodologies and expanding analytical approaches, it continues to play a central role in differential diagnosis, prognostic assessment, and integrated precision neurology.
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