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Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease
BACKGROUND AND PURPOSE: Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Neurological Association
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653627/ https://www.ncbi.nlm.nih.gov/pubmed/29057631 http://dx.doi.org/10.3988/jcn.2017.13.4.387 |
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author | Park, Kee Hyung Noh, Young Choi, Eun-Jung Kim, Hyungsik Chun, Sohyun Son, Young-Don |
author_facet | Park, Kee Hyung Noh, Young Choi, Eun-Jung Kim, Hyungsik Chun, Sohyun Son, Young-Don |
author_sort | Park, Kee Hyung |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD. METHODS: We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates. RESULTS: The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex. CONCLUSIONS: EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus. |
format | Online Article Text |
id | pubmed-5653627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Neurological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-56536272017-10-24 Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease Park, Kee Hyung Noh, Young Choi, Eun-Jung Kim, Hyungsik Chun, Sohyun Son, Young-Don J Clin Neurol Original Article BACKGROUND AND PURPOSE: Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) have different clinical and neuroimaging characteristics, but memory decline is usually present in both types. However, there have been few functional studies focused on the hippocampus in Alzheimer's disease. We therefore investigated the functional connectivity between the hippocampus and other brain regions using resting-state fMRI and compared the findings between EOAD and LOAD. METHODS: We recruited 13 patients with EOAD and 19 patients with LOAD at the early disease stage. Twenty-one young controls and ten old controls were also recruited. Each participant completed a standardized neuropsychological battery of tests and underwent T1-weighted structural MRI. fMRI data were acquired during the resting state using 3-T MRI. The functional connectivity to the hippocampus was calculated based on automated anatomical labeling templates. RESULTS: The functional connectivity from the hippocampus to other brain regions differed between patients with EOAD and LOAD. The LOAD patients showed decreased hippocampal connectivity to cortical regions, such as to the middle temporal cortex, orbitofrontal cortex, postcentral cortex, supramarginal cortex, and rolandic operculum. In contrast, EOAD patients showed smaller functional changes of the cortical regions connected to the hippocampus, such as the middle frontal cortex. CONCLUSIONS: EOAD and LOAD patients exhibited different hippocampal connectivity. The memory decline in EOAD may be due to brain areas other than the hippocampus. Korean Neurological Association 2017-10 2017-09-27 /pmc/articles/PMC5653627/ /pubmed/29057631 http://dx.doi.org/10.3988/jcn.2017.13.4.387 Text en Copyright © 2017 Korean Neurological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Park, Kee Hyung Noh, Young Choi, Eun-Jung Kim, Hyungsik Chun, Sohyun Son, Young-Don Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title | Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title_full | Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title_fullStr | Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title_full_unstemmed | Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title_short | Functional Connectivity of the Hippocampus in Early- and vs. Late-Onset Alzheimer's Disease |
title_sort | functional connectivity of the hippocampus in early- and vs. late-onset alzheimer's disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653627/ https://www.ncbi.nlm.nih.gov/pubmed/29057631 http://dx.doi.org/10.3988/jcn.2017.13.4.387 |
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