Literature DB >> 24434193

Brain atrophy in primary progressive aphasia involves the cholinergic basal forebrain and Ayala's nucleus.

Stefan J Teipel1, Wilhelm Flatz2, Nibal Ackl3, Michel Grothe4, Ingo Kilimann4, Arun L W Bokde5, Lea Grinberg6, Edson Amaro7, Vanja Kljajevic8, Eduardo Alho9, Christina Knels10, Anne Ebert11, Helmut Heinsen12, Adrian Danek3.   

Abstract

Primary progressive aphasia (PPA) is characterized by left hemispheric frontotemporal cortical atrophy. Evidence from anatomical studies suggests that the nucleus subputaminalis (NSP), a subnucleus of the cholinergic basal forebrain, may be involved in the pathological process of PPA. Therefore, we studied the pattern of cortical and basal forebrain atrophy in 10 patients with a clinical diagnosis of PPA and 18 healthy age-matched controls using high-resolution magnetic resonance imaging (MRI). We determined the cholinergic basal forebrain nuclei according to Mesulam's nomenclature and the NSP in MRI reference space based on histological sections and the MRI scan of a post-mortem brain in cranio. Using voxel-based analysis, we found left hemispheric cortical atrophy in PPA patients compared with controls, including prefrontal, lateral temporal and medial temporal lobe areas. We detected cholinergic basal forebrain atrophy in left predominant localizations of Ch4p, Ch4am, Ch4al, Ch3 and NSP. For the first time, we have described the pattern of basal forebrain atrophy in PPA and confirmed the involvement of NSP that had been predicted based on theoretical considerations. Our findings may enhance understanding of the role of cholinergic degeneration for the regional specificity of the cortical destruction leading to the syndrome of PPA.
© 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Cholinergic system; Diagnosis; Language; Nucleus subputaminalis; Post-mortem MRI; Primary progressive aphasia

Mesh:

Year:  2013        PMID: 24434193      PMCID: PMC4086659          DOI: 10.1016/j.pscychresns.2013.10.003

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  44 in total

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