TY - JOUR
T1 - White matter changes in preclinical Alzheimer's disease
T2 - A magnetic resonance imaging-diffusion tensor imaging study on cognitively normal older people with positive amyloid β protein 42 levels
AU - Molinuevo, José Luis
AU - Ripolles, Pablo
AU - Simó, Marta
AU - Lladó, Albert
AU - Olives, Jaume
AU - Balasa, Mircea
AU - Antonell, Anna
AU - Rodriguez-Fornells, Antoni
AU - Rami, Lorena
N1 - Funding Information:
The authors thank all the volunteers for participating in this study. This work was supported by Spanish Ministry of Science . Dr Lorena Rami is the recipient of a Miguel Servet grant as a senior investigator from the Spanish Ministry of Science ( CP08/00147 ). This study was funded by research grants from the Spanish Ministerio de Ciencia e Innovación to Dr Lorena Rami ( FIS PI11/01071 ), Fondo europeo de desarrollo regional, una manera de hacer Europa, grant from IMSERSO 197/2011 to Dr Molinuevo ( CONSOLIDER grant 2010-00045 and to the Innovative Medicines Initiative Joint Undertaking under grant agreement n°115568, resources of which are composed of financial contribution from the European Union's Seventh Framework Programme (FP7/2007–2013) and EFPIA companies' in kind contribution to Dr Lladó (PI11/00234), P. Ripollés (FPU AP2010-4179), and to Dr Rodríguez-Fornells (PSI2011-29219 and Generalitat de Catalunya grant 2009 SGR 93 ).
Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - The aim of this study was to use diffusion tensor imaging measures to determine the existence of white matter microstructural differences in the preclinical phases of Alzheimer's disease, assessing cognitively normal older individuals with positive amyloid β protein (Aβ42) levels (CN_Aβ42+) on the basis of normal cognition and cerebrospinal fluid Aβ42 levels below 500 pg/mL. Nineteen CN_Aβ42+ and 19 subjects with Aβ42 levels above 500 pg/mL (CN_Aβ42-) were included. We encountered increases in axial diffusivity (AxD) in CN_Aβ42+ relative to CN_Aβ42- in the corpus callosum, corona radiata, internal capsule, and superior longitudinal fasciculus bilaterally, and also in the left fornix, left uncinate fasciculus, and left inferior fronto-occipital fasciculus. However, no differences were found in other diffusion tensor imaging indexes. Cognitive reserve scores were positively associated with AxD exclusively in the CN_Aβ42+ group. The finding of AxD alteration together with preserved fractional anisotropy, mean diffusivity, and radial diffusivity indexes in the CN_Aβ42+ group may indicate that, subtle axonal changes may be happening in the preclinical phases of Alzheimer's disease, whereas white matter integrity is still widely preserved.
AB - The aim of this study was to use diffusion tensor imaging measures to determine the existence of white matter microstructural differences in the preclinical phases of Alzheimer's disease, assessing cognitively normal older individuals with positive amyloid β protein (Aβ42) levels (CN_Aβ42+) on the basis of normal cognition and cerebrospinal fluid Aβ42 levels below 500 pg/mL. Nineteen CN_Aβ42+ and 19 subjects with Aβ42 levels above 500 pg/mL (CN_Aβ42-) were included. We encountered increases in axial diffusivity (AxD) in CN_Aβ42+ relative to CN_Aβ42- in the corpus callosum, corona radiata, internal capsule, and superior longitudinal fasciculus bilaterally, and also in the left fornix, left uncinate fasciculus, and left inferior fronto-occipital fasciculus. However, no differences were found in other diffusion tensor imaging indexes. Cognitive reserve scores were positively associated with AxD exclusively in the CN_Aβ42+ group. The finding of AxD alteration together with preserved fractional anisotropy, mean diffusivity, and radial diffusivity indexes in the CN_Aβ42+ group may indicate that, subtle axonal changes may be happening in the preclinical phases of Alzheimer's disease, whereas white matter integrity is still widely preserved.
KW - Alzheimer's disease
KW - Cerebrospinal fluid
KW - Cognition
KW - Diagnosis
KW - Diffusion tensor imaging
KW - Preclinical phases
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U2 - 10.1016/j.neurobiolaging.2014.05.027
DO - 10.1016/j.neurobiolaging.2014.05.027
M3 - Article
C2 - 25002037
AN - SCOPUS:84910007752
SN - 0197-4580
VL - 35
SP - 2671
EP - 2680
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 12
ER -