2020-05-29T17:28:32Z
2020-05-29T17:28:32Z
2013-03-12
2020-05-29T17:28:32Z
Cognitive reserve capacity may increase tolerance of neurodegenerative processes. However, its role regarding amyloid-B (AB 42) deposition in cognitively normal subjects is not well understood. We aimed to investigate the association between areas showing A 42-related structural changes and cognitive reserve proxies in cognitively intact subjects showing normal or abnormal AB 42 cerebrospinal fluid (CSF) concentrations. Thirty-three subjects (aged 55-85) underwent lumbar puncture and high resolution anatomical magnetic resonance imaging analyzed by voxel-based morphometry and cortical thickness procedures. Subjects with abnormal A 42 CSF levels showed significant left hippocampal atrophy and greater cortical thinning in parietal, temporal, and frontal regions (including the supramarginal and the anterior cingulate gyrus) compared to subjects with normalA 42 CSF levels. Using a multivariate general linear model, we investigated the relationship between these areas and cognitive reserve proxies. We found a significant relationship between decreased volume of the left hippocampus or decreased cortical thickness of the right supramarginal gyrus and higher cognitive reserve proxies only in the group with abnormal A 42 CSF levels. Thus, subjects with abnormal A 42 CSF levels (which may be at a higher risk of developing Alzheimer's disease) and with high scores on cognitive reserve proxies may be tolerating a more advanced neurodegenerative process in critical cortical and subcortical regions. The present results emphasize the relevance of evaluating cognitive reserve proxies, as well as the importance of using neuroimaging techniques for early diagnosis in individuals with higher reserve.
Article
Published version
English
Imatges per ressonància magnètica; Envelliment cerebral; Malaltia d'Alzheimer; Líquid cefalorraquidi; Magnetic resonance imaging; Aging brain; Alzheimer's disease; Cerebrospinal fluid
IOS Press
Reproducció del document publicat a: https://doi.org/10.3233/JAD-121906
Journal of Alzheimer's Disease, 2013, vol. 35, num. 4, p. 715-726
https://doi.org/10.3233/JAD-121906
(c) Arenaza-Urquijo, Eider Maria et al., 2013