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Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease

Early diagnosis of dementia including Alzheimer’s disease (AD) is an urgent medical and welfare issue. However, to date, no simple biometrics have been available. We reported that blood DNA methylation levels of the COASY gene, which encodes coenzyme A synthase, were increased in individuals with AD...

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Autores principales: Kobayashi, Nobuyuki, Shinagawa, Shunichiro, Niimura, Hidehito, Kida, Hisashi, Nagata, Tomoyuki, Tagai, Kenji, Shimada, Kazuya, Oka, Naomi, Shikimoto, Ryo, Noda, Yoshihiro, Nakajima, Shinichiro, Mimura, Masaru, Shigeta, Masahiro, Kondo, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376092/
https://www.ncbi.nlm.nih.gov/pubmed/32699290
http://dx.doi.org/10.1038/s41598-020-69248-9
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author Kobayashi, Nobuyuki
Shinagawa, Shunichiro
Niimura, Hidehito
Kida, Hisashi
Nagata, Tomoyuki
Tagai, Kenji
Shimada, Kazuya
Oka, Naomi
Shikimoto, Ryo
Noda, Yoshihiro
Nakajima, Shinichiro
Mimura, Masaru
Shigeta, Masahiro
Kondo, Kazuhiro
author_facet Kobayashi, Nobuyuki
Shinagawa, Shunichiro
Niimura, Hidehito
Kida, Hisashi
Nagata, Tomoyuki
Tagai, Kenji
Shimada, Kazuya
Oka, Naomi
Shikimoto, Ryo
Noda, Yoshihiro
Nakajima, Shinichiro
Mimura, Masaru
Shigeta, Masahiro
Kondo, Kazuhiro
author_sort Kobayashi, Nobuyuki
collection PubMed
description Early diagnosis of dementia including Alzheimer’s disease (AD) is an urgent medical and welfare issue. However, to date, no simple biometrics have been available. We reported that blood DNA methylation levels of the COASY gene, which encodes coenzyme A synthase, were increased in individuals with AD and amnestic mild cognitive impairment (aMCI). The present study sought to replicate these findings with larger numbers of samples. Another objective was to clarify whether COASY methylation is associated with neurodegeneration through a comparison of AD, AD with cardiovascular disease (CVD), and vascular dementia (VaD). We measured blood COASY methylation levels in normal controls (NCs) (n = 200), and individuals with aMCI (n = 22), AD (n = 151), and VaD (n = 21). Compared with NCs, they were significantly higher in individuals with aMCI and AD. Further, they were significantly higher in AD patients without cardiovascular diseases compared to AD patients with them. These findings suggest that COASY methylation levels may be related to neurodegeneration in AD.
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spelling pubmed-73760922020-07-24 Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease Kobayashi, Nobuyuki Shinagawa, Shunichiro Niimura, Hidehito Kida, Hisashi Nagata, Tomoyuki Tagai, Kenji Shimada, Kazuya Oka, Naomi Shikimoto, Ryo Noda, Yoshihiro Nakajima, Shinichiro Mimura, Masaru Shigeta, Masahiro Kondo, Kazuhiro Sci Rep Article Early diagnosis of dementia including Alzheimer’s disease (AD) is an urgent medical and welfare issue. However, to date, no simple biometrics have been available. We reported that blood DNA methylation levels of the COASY gene, which encodes coenzyme A synthase, were increased in individuals with AD and amnestic mild cognitive impairment (aMCI). The present study sought to replicate these findings with larger numbers of samples. Another objective was to clarify whether COASY methylation is associated with neurodegeneration through a comparison of AD, AD with cardiovascular disease (CVD), and vascular dementia (VaD). We measured blood COASY methylation levels in normal controls (NCs) (n = 200), and individuals with aMCI (n = 22), AD (n = 151), and VaD (n = 21). Compared with NCs, they were significantly higher in individuals with aMCI and AD. Further, they were significantly higher in AD patients without cardiovascular diseases compared to AD patients with them. These findings suggest that COASY methylation levels may be related to neurodegeneration in AD. Nature Publishing Group UK 2020-07-22 /pmc/articles/PMC7376092/ /pubmed/32699290 http://dx.doi.org/10.1038/s41598-020-69248-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kobayashi, Nobuyuki
Shinagawa, Shunichiro
Niimura, Hidehito
Kida, Hisashi
Nagata, Tomoyuki
Tagai, Kenji
Shimada, Kazuya
Oka, Naomi
Shikimoto, Ryo
Noda, Yoshihiro
Nakajima, Shinichiro
Mimura, Masaru
Shigeta, Masahiro
Kondo, Kazuhiro
Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title_full Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title_fullStr Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title_full_unstemmed Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title_short Increased blood COASY DNA methylation levels a potential biomarker for early pathology of Alzheimer’s disease
title_sort increased blood coasy dna methylation levels a potential biomarker for early pathology of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376092/
https://www.ncbi.nlm.nih.gov/pubmed/32699290
http://dx.doi.org/10.1038/s41598-020-69248-9
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