Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/162049
Title: Interactive effect of age and APOE-ε4 allele load on white matter myelin content in cognitively normal middle-aged subjects
Author: Operto, Grégory
Molinuevo, José Luis
Cacciaglia, Raffaele
Falcon, Carles
Brugulat Serrat, Anna
Suárez Calvet, Marc
Grau Rivera, Oriol
Bargalló Alabart, Núria​
Moran, Sebastian
Esteller, Manel
Gispert, Juan Domingo
Keywords: Gens
Cognició
Malalties neurodegeneratives
Lípids
Mielina
Genes
Cognition
Neurodegenerative Diseases
Lipids
Myelin sheath
Issue Date: 16-Aug-2019
Publisher: Elsevier
Abstract: The apolipoprotein E gene (APOE) ε4 allele has a strong and manifold impact on cognition and neuroimaging phenotypes in cognitively normal subjects, including alterations in the white matter (WM) microstructure. Such alterations have often been regarded as a reflection of potential thinning of the myelin sheath along axons, rather than pure axonal degeneration. Considering the main role of APOE in brain lipid transport, characterizing the impact of APOE on the myelin coating is therefore of crucial interest, especially in healthy APOE-ε4 homozygous individuals, who are exposed to a twelve-fold higher risk of developing Alzheimer's disease (AD), compared to the rest of the population. We examined T1w/T2w ratio maps in 515 cognitively healthy middle-aged participants from the ALFA study (ALzheimer and FAmilies) cohort, a single-site population-based study enriched for AD risk (68 APOE-ε4 homozygotes, 197 heterozygotes, and 250 non-carriers). Using tract-based spatial statistics, we assessed the impact of age and APOE genotype on this ratio taken as an indirect descriptor of myelin content. Healthy APOE-ε4 carriers display decreased T1w/T2w ratios in extensive regions in a dose-dependent manner. These differences were found to interact with age, suggesting faster changes in individuals with more ε4 alleles. These results obtained with T1w/T2w ratios, confirm the increased vulnerability of WM tracts in APOE-ε4 healthy carriers. Early alterations of myelin content could be the result of the impaired function of the ε4 isoform of the APOE protein in cholesterol transport. These findings help to clarify the possible interactions between the APOE-dependent non-pathological burden and age-related changes potentially at the source of the AD pathological cascade.
Note: Reproducció del document publicat a: https://doi.org/10.1016/j.nicl.2019.101983
It is part of: Neuroimage-Clinical, 2019, vol. 24, p. 101983
URI: http://hdl.handle.net/2445/162049
Related resource: https://doi.org/10.1016/j.nicl.2019.101983
ISSN: 2213-1582
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Psicologia Clínica i Psicobiologia)

Files in This Item:
File Description SizeFormat 
691523.pdf5.14 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons