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Volume 30, Issue 1, Pages 112-124 (January 2009)


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Voxel-based mapping of brain gray matter volume and glucose metabolism profiles in normal aging

Grégoria Kalpouzosa, Gaël Chételata, Jean-Claude Baronbc, Brigitte Landeaua, Katell Mevela, Christine Godeaub, Louisa Barréd, Jean-Marc Constansf, Fausto Viaderae, Francis Eustachea, Béatrice DesgrangesaCorresponding Author Informationemail address

Received 3 August 2006; received in revised form 4 May 2007; accepted 21 May 2007. published online 16 July 2007.

Abstract 

With age, the brain undergoes both structural and functional alterations, probably resulting in reported cognitive declines. Relatively few investigations have sought to identify those areas that remain intact with aging, or undergo the least deterioration, which might underlie cognitive preservations. Our aim here was to establish a comprehensive profile of both structural and functional changes in the aging brain, using up-to-date voxel-based methodology (i.e. optimized voxel-based morphometry (VBM) procedure; resting-state 18FDG-PET with correction for partial volume effects (PVE)) in 45 optimally healthy subjects aged 20–83 years. Negative and positive correlations between age and both gray matter (GM) volume and 18FDG uptake were assessed. The frontal cortex manifested the greatest deterioration, both structurally and functionally, whereas the anterior hippocampus, the thalamus and (functionally) the posterior cingulate cortex were the least affected. Our results support the developmental theory which postulates that the first regions to emerge phylogenetically and ontogenetically are the most resistant to age effects, and the last ones the most vulnerable. Furthermore, the lesser affected anterior hippocampal region, together with the lesser functional alteration of the posterior cingulate cortex, appear to mark the parting of the ways between normal aging and Alzheimer's disease, which is characterized by early and prominent deterioration of both structures.

a Inserm-EPHE-Université de Caen/Basse-Normandie, Unité de Recherche E0218, GIP Cyceron, Caen, France

b Inserm, U 320, GIP Cyceron, Caen, France

c University of Cambridge, Department of Neurology, Cambridge, UK

d UMR CEA 2, FRE CNRS 2698, GIP Cyceron, Caen, France

e CHU Côte de Nacre, Service de neurologie Vastel, Caen, France

f CHU Côte de Nacre, Unité de neuroradiologie, Caen, France

Corresponding Author InformationCorresponding author at: Inserm-EPHE-Université de Caen/Basse-Normandie, Unité de Recherche E0218, Laboratoire de Neuropsychologie, CHU Côte de Nacre, 14033 Caen Cedex, France. Tel.: +33 2 31 06 51 95; fax: +33 2 31 06 51 98.

PII: S0197-4580(07)00230-8

doi:10.1016/j.neurobiolaging.2007.05.019


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