Age-Related Metabolic Profiles in Cognitively Healthy Elders: Results from a Voxel-Based [18F]Fluorodeoxyglucose―Positron-Emission Tomography Study with Partial Volume Effects Correction

• Published in: American journal of neuroradiology : AJNR Vol. 32; no. 3; pp. 560 - 565
• Main Authors: CURIATI, P. K, TAMASHIRO-DURAN, J. H, ALVES, T. C. T. F, DURAN, F. L. S, BUCHPIGUEL, C. A, SQUARZONI, P, ROMANO, D. C, VALLADA, H, MENEZES, P. R, SCAZUFCA, M, BUSATTO, G. F
• Format: Journal Article
• Language: English
• Published: Oak Brook, IL American Society of Neuroradiology 01.03.2011
• Subjects: Aged; Aging - metabolism; Algorithms; Biological and medical sciences; Brain - diagnostic imaging; Brain - metabolism; Female; Fluorodeoxyglucose F18 - pharmacokinetics; Functional; Humans; Image Enhancement - methods; Image Interpretation, Computer-Assisted - methods; Imaging, Three-Dimensional - methods; Investigative techniques, diagnostic techniques (general aspects); Male; Medical sciences; Nervous system; Nervous system involvement in other diseases. Miscellaneous; Neurology; Positron-Emission Tomography - methods; Radiodiagnosis. Nmr imagery. Nmr spectrometry; Radiopharmaceuticals - pharmacokinetics; Reference Values; Reproducibility of Results; Sensitivity and Specificity; 2-deoxy-2-fluoroglucose; Nervous system diseases; Radiodiagnosis; Voxel; Positron emission tomography; Corrections; Emission tomography
• ISSN: 0195-6108; 1936-959X
• DOI: 10.3174/ajnr.A2321

Functional brain variability has been scarcely investigated in cognitively healthy elderly subjects, and it is currently debated whether previous findings of regional metabolic variability are artifacts associated with brain atrophy. The primary purpose of this study was to test whether there is regional cerebral age-related hypometabolism specifically in later stages of life. MR imaging and FDG-PET data were acquired from 55 cognitively healthy elderly subjects, and voxel-based linear correlations between age and GM volume or regional cerebral metabolism were conducted by using SPM5 in images with and without correction for PVE. To investigate sex-specific differences in the pattern of brain aging, we repeated the above voxelwise calculations after dividing our sample by sex. Our analysis revealed 2 large clusters of age-related metabolic decrease in the overall sample, 1 in the left orbitofrontal cortex and the other in the right temporolimbic region, encompassing the hippocampus, the parahippocampal gyrus, and the amygdala. The division of our sample by sex revealed significant sex-specific age-related metabolic decrease in the left temporolimbic region of men and in the left dorsolateral frontal cortex of women. When we applied atrophy correction to our PET data, none of the above-mentioned correlations remained significant. Our findings suggest that age-related functional brain variability in cognitively healthy elderly individuals is largely secondary to the degree of regional brain atrophy, and the findings provide support to the notion that appropriate PVE correction is a key tool in neuroimaging investigations.