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Regional Cerebral Glucose Metabolism in Healthy Volunteers Determined by Fluordeoxyglucose Positron Emission Tomography: Appearance and Variance in the Transaxial, Coronal, and Sagittal Planes
Abstract
Purpose In this study, the contribution of the transaxial, coronal, and sagittal planes in evaluations of regional cerebral glucose metabolism was investigated in healthy volunteers as determined by fluorine-18-labeled 2-deoxy-2-fluoro-D-glucose (FDG) and high-resolution positron emission tomography (PET). Methods One hundred twenty-seven healthy right-handed volunteers were injected with 4.2 MBq/kg (0.11 mCi) body weight FDG and imaged in a PENN PET H 240 scanner. Images were corrected for scatter and random coincidences and reconstructed in all three planes into 6- to 8-mm-thick slices. The reconstructed images were corrected for attenuation using the Chang algorithm. The transverse, coronal, and sagittal images were read independently of each other using a qualitative scale in which 1 = equal to, 2 = mildly, 3 = moderately, and 4 = markedly less than the area with the highest glucose metabolism in the respective plane. Results The areas with the highest glucose metabolisms were the posterior cingulate gyri with mean scores of 1.1 to 1.2, thalami (1.2 to 1.3), basal ganglia (1.5 to 1.9), and visual cortex (1.6). The lowest values were found in the occipital cortex (2.7 to 2.8) and the cerebellum (2.3 to 2.4). Whereas reliable analysis of the mesial temporal aspects was not feasible in the sagittal plane, the anterior poles of the temporal and frontal lobes could not be evaluated in the coronal or the inferior temporal areas in the transaxial slices. In all three planes, reg…
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Availability of glucose becomes limited during various stress conditions, such as brain ageing.
“However, availability of glucose becomes limited during various stress conditions, such as brain ageing34–39.”
From Interaction of sortilin with apolipoprotein E3 enables neurons to use long-chain fatty acids as alternative metabolic fuel (2025) · cites this paper as [34]
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Liang, W. S., Reiman, E. M., Valla, J., Dunckley, T., Beach, T. G., Grover, A., Niedzielko, T. L., Schneider, L. E., Mastroeni, D., Caselli, R., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709259105 · Cited by 585
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The role of glucose transporters in brain disease: Diabetes and Alzheimer’s disease
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Brain FDG PET study of normal aging in Japanese: effect of atrophy correction
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Yoshizawa, H., Gazes, Y., Stern, Y., Miyata, Y., & Uchiyama, S. (2014) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2013.10.009 · Cited by 100
Greda, A. K., Gomes, J. P., Schmidt-Krueger, V., Zurawska-Plaksej, E., Fritsche-Guenther, R., Rudolph, I.-M., Telugu, N. S., Cömert, C., Kirwan, J., Kunz, S., et al. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01389-5 · Cited by 21
Metadata
- Authors
- ANÇEVIĆ, V., ALAVI, A., SOUDER, E., MOZLEY, P. D., GUR, R. E., BÉNARD, F., & MUNZ, D. L.
- Venue
- Clinical Nuclear Medicine
- Published
- 2000-08
- Volume
- 25
- Issue
- 8
- Pages
- 596-602
- ISSN
- 0363-9762
- Cited by
- 29
- References
- 2
- Language
- en
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