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Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study
Diabetes mellitus (DM) is considered to be a risk factor for dementia including Alzheimer's disease (AD). However, the molecular mechanism underlying this risk is not well understood. We examined gene expression profiles in postmortem human brains donated for the Hisayama study. Three-way analy...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128707/ https://www.ncbi.nlm.nih.gov/pubmed/23595620 http://dx.doi.org/10.1093/cercor/bht101 |
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author | Hokama, Masaaki Oka, Sugako Leon, Julio Ninomiya, Toshiharu Honda, Hiroyuki Sasaki, Kensuke Iwaki, Toru Ohara, Tomoyuki Sasaki, Tomio LaFerla, Frank M. Kiyohara, Yutaka Nakabeppu, Yusaku |
author_facet | Hokama, Masaaki Oka, Sugako Leon, Julio Ninomiya, Toshiharu Honda, Hiroyuki Sasaki, Kensuke Iwaki, Toru Ohara, Tomoyuki Sasaki, Tomio LaFerla, Frank M. Kiyohara, Yutaka Nakabeppu, Yusaku |
author_sort | Hokama, Masaaki |
collection | PubMed |
description | Diabetes mellitus (DM) is considered to be a risk factor for dementia including Alzheimer's disease (AD). However, the molecular mechanism underlying this risk is not well understood. We examined gene expression profiles in postmortem human brains donated for the Hisayama study. Three-way analysis of variance of microarray data from frontal cortex, temporal cortex, and hippocampus was performed with the presence/absence of AD and vascular dementia, and sex, as factors. Comparative analyses of expression changes in the brains of AD patients and a mouse model of AD were also performed. Relevant changes in gene expression identified by microarray analysis were validated by quantitative real-time reverse-transcription polymerase chain reaction and western blotting. The hippocampi of AD brains showed the most significant alteration in gene expression profile. Genes involved in noninsulin-dependent DM and obesity were significantly altered in both AD brains and the AD mouse model, as were genes related to psychiatric disorders and AD. The alterations in the expression profiles of DM-related genes in AD brains were independent of peripheral DM-related abnormalities. These results indicate that altered expression of genes related to DM in AD brains is a result of AD pathology, which may thereby be exacerbated by peripheral insulin resistance or DM. |
format | Online Article Text |
id | pubmed-4128707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41287072014-08-12 Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study Hokama, Masaaki Oka, Sugako Leon, Julio Ninomiya, Toshiharu Honda, Hiroyuki Sasaki, Kensuke Iwaki, Toru Ohara, Tomoyuki Sasaki, Tomio LaFerla, Frank M. Kiyohara, Yutaka Nakabeppu, Yusaku Cereb Cortex Articles Diabetes mellitus (DM) is considered to be a risk factor for dementia including Alzheimer's disease (AD). However, the molecular mechanism underlying this risk is not well understood. We examined gene expression profiles in postmortem human brains donated for the Hisayama study. Three-way analysis of variance of microarray data from frontal cortex, temporal cortex, and hippocampus was performed with the presence/absence of AD and vascular dementia, and sex, as factors. Comparative analyses of expression changes in the brains of AD patients and a mouse model of AD were also performed. Relevant changes in gene expression identified by microarray analysis were validated by quantitative real-time reverse-transcription polymerase chain reaction and western blotting. The hippocampi of AD brains showed the most significant alteration in gene expression profile. Genes involved in noninsulin-dependent DM and obesity were significantly altered in both AD brains and the AD mouse model, as were genes related to psychiatric disorders and AD. The alterations in the expression profiles of DM-related genes in AD brains were independent of peripheral DM-related abnormalities. These results indicate that altered expression of genes related to DM in AD brains is a result of AD pathology, which may thereby be exacerbated by peripheral insulin resistance or DM. Oxford University Press 2014-09 2013-04-17 /pmc/articles/PMC4128707/ /pubmed/23595620 http://dx.doi.org/10.1093/cercor/bht101 Text en © The Author 2013. Published by Oxford University Press. 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 non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Hokama, Masaaki Oka, Sugako Leon, Julio Ninomiya, Toshiharu Honda, Hiroyuki Sasaki, Kensuke Iwaki, Toru Ohara, Tomoyuki Sasaki, Tomio LaFerla, Frank M. Kiyohara, Yutaka Nakabeppu, Yusaku Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title | Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title_full | Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title_fullStr | Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title_full_unstemmed | Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title_short | Altered Expression of Diabetes-Related Genes in Alzheimer's Disease Brains: The Hisayama Study |
title_sort | altered expression of diabetes-related genes in alzheimer's disease brains: the hisayama study |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4128707/ https://www.ncbi.nlm.nih.gov/pubmed/23595620 http://dx.doi.org/10.1093/cercor/bht101 |
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