Journal
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
Volume 49, Issue 2, Pages 664-680Publisher
SPRINGER
DOI: 10.1007/s00259-021-05518-6
Keywords
Ageing; PET; MR; Structural MRI; Tractography
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The study found that as individuals age, there is a reduction in gray matter density, decrease in glucose metabolism, and weakening of white matter integrity in the brain. White matter tracts connecting regions with declining glucose metabolism were identified, showing correlations with changes in fractional anisotropy and mean diffusivity. Further research is needed to explore the temporal course and potential causality between ageing effects on glucose metabolism and white matter integrity.
Purpose Human ageing is associated with a regional reduction in cerebral neuronal activity as assessed by numerous studies on brain glucose metabolism and perfusion, grey matter (GM) density and white matter (WM) integrity. As glucose metabolism may impact energetics to maintain myelin integrity, but changes in functional connectivity may also alter regional metabolism, we conducted a cross-sectional simultaneous FDG PET/MR study in a large cohort of healthy volunteers with a wide age range, to directly assess the underlying associations between reduced glucose metabolism, GM atrophy and decreased WM integrity in a single ageing cohort. Methods In 94 healthy subjects between 19.9 and 82.5 years (mean 50.1 +/- 17.1; 47 M/47F, MMSE >= 28), simultaneous FDG-PET, structural MR and diffusion tensor imaging (DTI) were performed. Voxel-wise associations between age and grey matter (GM) density, RBV partial-volume corrected (PVC) glucose metabolism, white matter (WM) fractional anisotropy (FA) and mean diffusivity (MD), and age were assessed. Clusters representing changes in glucose metabolism correlating significantly with ageing were used as seed regions for tractography. Both linear and quadratic ageing models were investigated. Results An expected age-related reduction in GM density was observed bilaterally in the frontal, lateral and medial temporal cortex, striatum and cerebellum. After PVC, relative FDG uptake was negatively correlated with age in the inferior and midfrontal, cingulate and parietal cortex and subcortical regions, bilaterally. FA decreased with age throughout the entire brain WM. Four white matter tracts were identified connecting brain regions with declining glucose metabolism with age. Within these, relative FDG uptake in both origin and target clusters correlated positively with FA (0.32 <= r <= 0.71) and negatively with MD (- 0.75 <= r <= - 0.41). Conclusion After appropriate PVC, we demonstrated that regional cerebral glucose metabolic declines with age and that these changes are related to microstructural changes in the interconnecting WM tracts. The temporal course and potential causality between ageing effects on glucose metabolism and WM integrity should be further investigated in longitudinal cohort PET/MR studies.
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