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Mapping the Progression of Atrophy in Early- and Late-Onset Alzheimer's Disease.


ABSTRACT: The term early-onset Alzheimer's disease (EOAD) identifies patients who meet criteria for AD, but show onset of symptoms before the age of 65. We map progression of gray matter atrophy in EOAD patients compared to late-onset AD (LOAD). T1-weighted MRI scans were obtained at diagnosis and one-year follow-up from 15 EOAD, 10 LOAD, and 38 age-matched controls. Voxel-based and tensor-based morphometry were used, respectively, to assess the baseline and progression of atrophy. At baseline, EOAD patients already showed a widespread atrophy in temporal, parietal, occipital, and frontal cortices. After one year, EOAD had atrophy progression in medial temporal and medial parietal cortices. At baseline, LOAD patients showed atrophy in the medial temporal regions only, and, after one year, an extensive pattern of atrophy progression in the same neocortical cortices of EOAD. Although atrophy mainly involved different lateral neocortical or medial temporal hubs at baseline, it eventually progressed along the same brain default-network regions in both groups. The cortical region showing a significant progression in both groups was the medial precuneus/posterior cingulate.

SUBMITTER: Migliaccio R 

PROVIDER: S-EPMC4559486 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Mapping the Progression of Atrophy in Early- and Late-Onset Alzheimer's Disease.

Migliaccio Raffaella R   Agosta Federica F   Possin Katherine L KL   Canu Elisa E   Filippi Massimo M   Rabinovici Gil D GD   Rosen Howard J HJ   Miller Bruce L BL   Gorno-Tempini Maria Luisa ML  

Journal of Alzheimer's disease : JAD 20150101 2


The term early-onset Alzheimer's disease (EOAD) identifies patients who meet criteria for AD, but show onset of symptoms before the age of 65. We map progression of gray matter atrophy in EOAD patients compared to late-onset AD (LOAD). T1-weighted MRI scans were obtained at diagnosis and one-year follow-up from 15 EOAD, 10 LOAD, and 38 age-matched controls. Voxel-based and tensor-based morphometry were used, respectively, to assess the baseline and progression of atrophy. At baseline, EOAD patie  ...[more]

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