| Literature DB >> 24503619 |
Ingo Kilimann1, Michel Grothe2, Helmut Heinsen3, Eduardo Joaquim Lopez Alho3, Lea Grinberg4, Edson Amaro5, Gláucia Aparecida Bento Dos Santos5, Rafael Emídio da Silva5, Alex J Mitchell6, Giovanni B Frisoni7, Arun L W Bokde8, Andreas Fellgiebel9, Massimo Filippi10, Harald Hampel11, Stefan Klöppel12, Stefan J Teipel1.
Abstract
Histopathological studies in Alzheimer's disease (AD) suggest severe and region-specific neurodegeneration of the basal forebrain cholinergic system (BFCS). Here, we studied the between-center reliability and diagnostic accuracy of MRI-based BFCS volumetry in a large multicenter data set, including participants with prodromal (n = 41) or clinically manifest AD (n = 134) and 148 cognitively healthy controls. Atrophy was determined using voxel-based and region-of-interest based analyses of high-dimensionally normalized MRI scans using a newly created map of the BFCS based on postmortem in cranio MRI and histology. The AD group showed significant volume reductions of all subregions of the BFCS, which were most pronounced in the posterior nucleus basalis Meynert (NbM). The mild cognitive impairment-AD group showed pronounced volume reductions in the posterior NbM, but preserved volumes of anterior-medial regions. Diagnostic accuracy of posterior NbM volume was superior to hippocampus volume in both groups, despite higher multicenter variability of the BFCS measurements. The data of our study suggest that BFCS morphometry may provide an emerging biomarker in AD.Entities:
Keywords: Atrophy; European DTI Study on Dementia; biomarker; cholinergic system; dementia
Mesh:
Year: 2014 PMID: 24503619 PMCID: PMC4120953 DOI: 10.3233/JAD-132345
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472