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Basal Ganglia and Frontal Lobe Glucose Metabolism
Author(s) -
Goldman Serge,
Dethy Sophie,
Lotstra Françoise,
Biver Françoise,
Stanus Etienne,
Wikler David,
Hildebrand J.,
Mendlewicz Julien,
Luxen André
Publication year - 1995
Publication title -
journal of neuroimaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.822
H-Index - 64
eISSN - 1552-6569
pISSN - 1051-2284
DOI - 10.1111/jon199554219
Subject(s) - basal ganglia , basal (medicine) , frontal lobe , basal metabolic rate , caudate nucleus , medicine , positron emission tomography , frontal cortex , cortex (anatomy) , reproducibility , nuclear medicine , endocrinology , neuroscience , biology , central nervous system , chemistry , insulin , psychiatry , chromatography
Positron emission tomography (PET) with 18 F‐fluoro‐2‐deoxy‐Dglucose (FDG) is frequently used to study the metabolic correlates of movement and mental disorders. These studies generally focus on changes in the frontal cortex and the basal ganglia. The reproducibility of glucose metabolism estimates in these structures was tested in 13 normal subjects studied at rest usmg a standard and simple protocol. A reproducible dorsoventral metabolic gradient was demonstrated in the frontal cortex. Such a grad1ent was not present in the basal ganglia when the upper region of interest in the caudate nucleus, where the lower metabolic rate of glucose was probably attnbutable to partial volume effects, was not considered. Absolute values of glucose metabolic rates varied by 6.4 to 12.5% m the frontal cortex and by 6.8 to 14.7% in the basal ganglia. Vamtions in normalized values in the basal gangl1a ranged from 4.0 to 8.6%. The number of subjects required to detect statistical differences in group companson or in test‐retest studies was calculated for different anticipated levels of change. With the variability detected in this expenment, less than 10 subjects were expected to be sufficient to detect a 15% change in most regions and in both types of studies.