dc.contributor.author
Pujol Nuez, Jesús
dc.contributor.author
Fenoll, Raquel
dc.contributor.author
Ribas-Vidal, Núria
dc.contributor.author
Martínez Vilavella, Gerard
dc.contributor.author
Blanco Hinojo, Laura
dc.contributor.author
García Alba, Javier
dc.contributor.author
Deus Yela, Juan
dc.contributor.author
Novell, Ramon
dc.contributor.author
Esteba-Castillo, Susanna
dc.identifier
https://ddd.uab.cat/record/195072
dc.identifier
urn:10.1016/j.nicl.2018.01.024
dc.identifier
urn:oai:ddd.uab.cat:195072
dc.identifier
urn:pmid:29868444
dc.identifier
urn:pmcid:PMC5984600
dc.identifier
urn:pmc-uid:5984600
dc.identifier
urn:articleid:22131582v18p160
dc.identifier
urn:scopus_id:85041632803
dc.identifier
urn:wos_id:000433169000016
dc.identifier
urn:altmetric_id:43498659
dc.identifier
urn:recercauab:ARE-87868
dc.identifier
urn:oai:egreta.uab.cat:publications/bbf5b96b-cac2-4fbb-a026-38b9329f5c4c
dc.identifier
urn:oai:pubmedcentral.nih.gov:5984600
dc.description.abstract
We longitudinally assessed Down syndrome individuals at the age of risk of developing dementia to measure changes in brain anatomy and their relationship to cognitive impairment progression. Forty-two Down syndrome individuals were initially included, of whom 27 (mean age 46.8 years) were evaluable on the basis of completing the 2-year follow-up and success in obtaining good quality MRI exams. Voxel-based morphometry was used to estimate regional brain volumes at baseline and follow-up on 3D anatomical images. Longitudinal volume changes for the group and their relationship with change in general cognitive status and specific cognitive domains were mapped. As a group, significant volume reduction was identified in the substantia innominata region of the basal forebrain, hippocampus, lateral temporal cortex and left arcuate fasciculus. Volume reduction in the substantia innominata and hippocampus was more prominent in individuals whose clinical status changed from cognitively stable to mild cognitive impairment or dementia during the follow-up. Relevantly, longitudinal memory score change was specifically associated with volume change in the hippocampus, prospective memory with prefrontal lobe and verbal comprehension with language-related brain areas. Results are notably concordant with the well-established anatomical changes signaling the progression to dementia in Alzheimer's disease, despite the dense baseline pathology that developmentally accumulates in Down syndrome. This commonality supports the potential value of Down syndrome as a genetic model of Alzheimer's neurodegeneration and may serve to further support the view that Down syndrome patients are best candidates to benefit from treatment research in Alzheimer's disease.
dc.format
application/pdf
dc.relation
Instituto de Salud Carlos III PI12/02019
dc.relation
Instituto de Salud Carlos III PSI-2014-53524-P
dc.relation
NeuroImage. Clinical ; Vol. 18 (january 2018), p. 160-166
dc.rights
Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.
dc.rights
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Cognitive aging
dc.title
A longitudinal study of brain anatomy changes preceding dementia in Down syndrome