6533b832fe1ef96bd129ab4d
RESEARCH PRODUCT
Towards a unified analysis of brain maturation and aging across the entire lifespan: A MRI analysis
Pierrick CoupéPierrick CoupéJosé E. RomeroEnrique LanuzaAlzheimer's Disease Neuroimaging InitiativeGwénaëlle CathelineJosé V. Manjónsubject
CerebellumRadiological and Ultrasound TechnologyCerebellum maturation05 social sciencesBrain maturationContext (language use)Degeneration (medical)Slow growth050105 experimental psychologyAccurate segmentation03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureNeurologymedicine0501 psychology and cognitive sciencesRadiology Nuclear Medicine and imagingSegmentationNeurology (clinical)AnatomyPsychologyNeuroscience030217 neurology & neurosurgerydescription
Previous literature about the structural characterization of the human cerebellum is related to the context of a specific pathology or focused in a restricted age range. In fact, studies about the cerebellum maturation across the lifespan are scarce and most of them considered the cerebellum as a whole without investigating each lobule. This lack of study can be explained by the lack of both accurate segmentation methods and data availability. Fortunately, during the last years, several cerebellum segmentation methods have been developed and many databases comprising subjects of different ages have been made publically available. This fact opens an opportunity window to obtain a more extensive analysis of the cerebellum maturation and aging. In this study, we have used a recent state-of-the-art cerebellum segmentation method called CERES and a large data set (N = 2,831 images) from healthy controls covering the entire lifespan to provide a model for 12 cerebellum structures (i.e., lobules I-II, III, IV, VI, Crus I, Crus II, VIIB, VIIIA, VIIIB, IX, and X). We found that lobules have generally an evolution that follows a trajectory composed by a fast growth and a slow degeneration having sometimes a plateau for absolute volumes, and a decreasing tendency (faster in early ages) for normalized volumes. Special consideration is dedicated to Crus II, where slow degeneration appears to stabilize in elder ages for absolute volumes, and to lobule X, which does not present any fast growth during childhood in absolute volumes and shows a slow growth for normalized volumes.
year | journal | country | edition | language |
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2017-07-24 | Human Brain Mapping |