Structural hippocampal network alterations during healthy aging: a multi-modal MRI study

• Published in: Frontiers in aging neuroscience Vol. 5; p. 84
• Main Authors: Pelletier, Amandine, Periot, Olivier, Dilharreguy, Bixente, Hiba, Bassem, Bordessoules, Martine, Pérès, Karine, Amieva, Hélène, Dartigues, Jean-François, Allard, Michèle, Catheline, Gwénaëlle
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 2013; Frontiers Media S.A
• Subjects: Age; Aging; Alzheimer's disease; Anisotropy; Atrophy; Cingulum; Cognitive ability; Dementia; Dementia disorders; DTI; Fornix; healthy aging; hippocampal atrophy; Hippocampus; Limbic System; Magnetic resonance imaging; Memory; Neurodegeneration; Neuroimaging; Neuroscience; NMR; Nuclear magnetic resonance; Substantia alba; France; mode of anisotropy; cingulum; DTI; limbic system; fornix; hippocampal atrophy; healthy aging
• ISSN: 1663-4365; 1663-4365
• DOI: 10.3389/fnagi.2013.00084

While hippocampal atrophy has been described during healthy aging, few studies have examined its relationship with the integrity of White Matter (WM) connecting tracts of the limbic system. This investigation examined WM structural damage specifically related to hippocampal atrophy in healthy aging subjects (n = 129), using morphological MRI to assess hippocampal volume and Diffusion Tensor Imaging (DTI) to assess WM integrity. Subjects with Mild Cognitive Impairment (MCI) or dementia were excluded from the analysis. In our sample, increasing age was significantly associated with reduced hippocampal volume and reduced Fractional Anisotropy (FA) at the level of the fornix and the cingulum bundle. The findings also demonstrate that hippocampal atrophy was specifically associated with reduced FA of the fornix bundle, but it was not related to alteration of the cingulum bundle. Our results indicate that the relationship between hippocampal atrophy and fornix FA values is not due to an independent effect of age on both structures. A recursive regression procedure was applied to evaluate sequential relationships between the alterations of these two brain structures. When both hippocampal atrophy and fornix FA values were included in the same model to predict age, fornix FA values remained significant whereas hippocampal atrophy was no longer significantly associated with age. According to this latter finding, hippocampal atrophy in healthy aging could be mediated by a loss of fornix connections. Structural alterations of this part of the limbic system, which have been associated with neurodegeneration in Alzheimer's disease, result at least in part from the aging process.