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Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment

Increased fMRI activation in the hippocampus is recognized as a signature characteristic of the amnestic mild cognitive impairment (aMCI) stage of Alzheimer's disease (AD). Previous work has localized this increased activation to the dentate gyrus/CA3 subregion of the hippocampus and showed a c...

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Autores principales: Tran, Tammy T., Speck, Caroline L., Pisupati, Aparna, Gallagher, Michela, Bakker, Arnold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217770/
https://www.ncbi.nlm.nih.gov/pubmed/28070483
http://dx.doi.org/10.1016/j.nicl.2016.12.002
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author Tran, Tammy T.
Speck, Caroline L.
Pisupati, Aparna
Gallagher, Michela
Bakker, Arnold
author_facet Tran, Tammy T.
Speck, Caroline L.
Pisupati, Aparna
Gallagher, Michela
Bakker, Arnold
author_sort Tran, Tammy T.
collection PubMed
description Increased fMRI activation in the hippocampus is recognized as a signature characteristic of the amnestic mild cognitive impairment (aMCI) stage of Alzheimer's disease (AD). Previous work has localized this increased activation to the dentate gyrus/CA3 subregion of the hippocampus and showed a correlation with memory impairments in those patients. Increased hippocampal activation has also been reported in carriers of the ApoE-4 allelic variation independently of mild cognitive impairment although these findings were not localized to a hippocampal subregion. To assess the ApoE-4 contribution to increased hippocampal fMRI activation, patients with aMCI genotyped for ApoE-4 status and healthy age-matched control participants completed a high-resolution fMRI scan while performing a memory task designed to tax hippocampal subregion specific functions. Consistent with previous reports, patients with aMCI showed increased hippocampal activation in the left dentate gyrus/CA3 region of the hippocampus as well as memory task errors attributable to this subregion. However, this increased fMRI activation in the hippocampus did not differ between ApoE-4 carriers and ApoE-4 non-carriers and the proportion of memory errors attributable to dentate gyrus/CA3 function did not differ between ApoE-4 carriers and ApoE-4 non-carriers. These results indicate that increased fMRI activation of the hippocampus observed in patients with aMCI is independent of ApoE-4 status and that ApoE-4 does not contribute to the dysfunctional hippocampal activation or the memory errors attributable to this subregion in these patients.
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spelling pubmed-52177702017-01-09 Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment Tran, Tammy T. Speck, Caroline L. Pisupati, Aparna Gallagher, Michela Bakker, Arnold Neuroimage Clin Regular Article Increased fMRI activation in the hippocampus is recognized as a signature characteristic of the amnestic mild cognitive impairment (aMCI) stage of Alzheimer's disease (AD). Previous work has localized this increased activation to the dentate gyrus/CA3 subregion of the hippocampus and showed a correlation with memory impairments in those patients. Increased hippocampal activation has also been reported in carriers of the ApoE-4 allelic variation independently of mild cognitive impairment although these findings were not localized to a hippocampal subregion. To assess the ApoE-4 contribution to increased hippocampal fMRI activation, patients with aMCI genotyped for ApoE-4 status and healthy age-matched control participants completed a high-resolution fMRI scan while performing a memory task designed to tax hippocampal subregion specific functions. Consistent with previous reports, patients with aMCI showed increased hippocampal activation in the left dentate gyrus/CA3 region of the hippocampus as well as memory task errors attributable to this subregion. However, this increased fMRI activation in the hippocampus did not differ between ApoE-4 carriers and ApoE-4 non-carriers and the proportion of memory errors attributable to dentate gyrus/CA3 function did not differ between ApoE-4 carriers and ApoE-4 non-carriers. These results indicate that increased fMRI activation of the hippocampus observed in patients with aMCI is independent of ApoE-4 status and that ApoE-4 does not contribute to the dysfunctional hippocampal activation or the memory errors attributable to this subregion in these patients. Elsevier 2016-12-07 /pmc/articles/PMC5217770/ /pubmed/28070483 http://dx.doi.org/10.1016/j.nicl.2016.12.002 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Tran, Tammy T.
Speck, Caroline L.
Pisupati, Aparna
Gallagher, Michela
Bakker, Arnold
Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title_full Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title_fullStr Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title_full_unstemmed Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title_short Increased hippocampal activation in ApoE-4 carriers and non-carriers with amnestic mild cognitive impairment
title_sort increased hippocampal activation in apoe-4 carriers and non-carriers with amnestic mild cognitive impairment
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217770/
https://www.ncbi.nlm.nih.gov/pubmed/28070483
http://dx.doi.org/10.1016/j.nicl.2016.12.002
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