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Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases

BACKGROUND: Cyclin-dependent kinase inhibitor 2A (CDKN2A) is an important gene in cellular senescence and aging. OBJECTIVE: This study assessed the utility of blood CDKN2A mRNA expression levels and methylation status as a potential biomarker for aging and the pathogenesis of Alzheimer’s disease (AD...

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Autores principales: Mori, Hiroaki, Funahashi, Yu, Yoshino, Yuta, Kumon, Hiroshi, Ozaki, Yuki, Yamazaki, Kiyohiro, Ochi, Shinichiro, Tachibana, Ayumi, Yoshida, Taku, Shimizu, Hideaki, Mori, Takaaki, Iga, Jun-ichi, Ueno, Shu-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461666/
https://www.ncbi.nlm.nih.gov/pubmed/34219731
http://dx.doi.org/10.3233/JAD-210483
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author Mori, Hiroaki
Funahashi, Yu
Yoshino, Yuta
Kumon, Hiroshi
Ozaki, Yuki
Yamazaki, Kiyohiro
Ochi, Shinichiro
Tachibana, Ayumi
Yoshida, Taku
Shimizu, Hideaki
Mori, Takaaki
Iga, Jun-ichi
Ueno, Shu-ichi
author_facet Mori, Hiroaki
Funahashi, Yu
Yoshino, Yuta
Kumon, Hiroshi
Ozaki, Yuki
Yamazaki, Kiyohiro
Ochi, Shinichiro
Tachibana, Ayumi
Yoshida, Taku
Shimizu, Hideaki
Mori, Takaaki
Iga, Jun-ichi
Ueno, Shu-ichi
author_sort Mori, Hiroaki
collection PubMed
description BACKGROUND: Cyclin-dependent kinase inhibitor 2A (CDKN2A) is an important gene in cellular senescence and aging. OBJECTIVE: This study assessed the utility of blood CDKN2A mRNA expression levels and methylation status as a potential biomarker for aging and the pathogenesis of Alzheimer’s disease (AD). METHODS: The correlation between CDKN2A mRNA expression levels and age was examined in 45 healthy subjects, after which mRNA expression levels were compared among 46 AD patients, 20 mild cognitive impairment due to AD patients, 21 Parkinson’s disease patients, 21 dementia with Lewy bodies patients, and 55 older healthy controls. The methylation rates of the second exon of the CDKN2A gene, known to influence its expression levels, was also examined. RESULTS: A significant correlation between CDKN2A mRNA expression levels and age was found (Spearman’s rank correlation coefficient: r = 0.407, p = 0.005). CDKN2A mRNA expression levels in blood were significantly decreased in AD patients, although those of healthy controls were significantly increased with age. Further, only in AD patients were CDKN2A mRNA expression levels significantly and positively correlated with methylation rates. CONCLUSION: Although further research with a larger sample size is needed to elucidate the relationships between CDKN2A gene expression in blood and the development of other neurodegenerative diseases, CDKN2A mRNA expression in blood may be a biomarker for differentiating AD from normal aging and other neurodegenerative diseases.
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spelling pubmed-84616662021-10-08 Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases Mori, Hiroaki Funahashi, Yu Yoshino, Yuta Kumon, Hiroshi Ozaki, Yuki Yamazaki, Kiyohiro Ochi, Shinichiro Tachibana, Ayumi Yoshida, Taku Shimizu, Hideaki Mori, Takaaki Iga, Jun-ichi Ueno, Shu-ichi J Alzheimers Dis Research Article BACKGROUND: Cyclin-dependent kinase inhibitor 2A (CDKN2A) is an important gene in cellular senescence and aging. OBJECTIVE: This study assessed the utility of blood CDKN2A mRNA expression levels and methylation status as a potential biomarker for aging and the pathogenesis of Alzheimer’s disease (AD). METHODS: The correlation between CDKN2A mRNA expression levels and age was examined in 45 healthy subjects, after which mRNA expression levels were compared among 46 AD patients, 20 mild cognitive impairment due to AD patients, 21 Parkinson’s disease patients, 21 dementia with Lewy bodies patients, and 55 older healthy controls. The methylation rates of the second exon of the CDKN2A gene, known to influence its expression levels, was also examined. RESULTS: A significant correlation between CDKN2A mRNA expression levels and age was found (Spearman’s rank correlation coefficient: r = 0.407, p = 0.005). CDKN2A mRNA expression levels in blood were significantly decreased in AD patients, although those of healthy controls were significantly increased with age. Further, only in AD patients were CDKN2A mRNA expression levels significantly and positively correlated with methylation rates. CONCLUSION: Although further research with a larger sample size is needed to elucidate the relationships between CDKN2A gene expression in blood and the development of other neurodegenerative diseases, CDKN2A mRNA expression in blood may be a biomarker for differentiating AD from normal aging and other neurodegenerative diseases. IOS Press 2021-08-17 /pmc/articles/PMC8461666/ /pubmed/34219731 http://dx.doi.org/10.3233/JAD-210483 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://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 Research Article
Mori, Hiroaki
Funahashi, Yu
Yoshino, Yuta
Kumon, Hiroshi
Ozaki, Yuki
Yamazaki, Kiyohiro
Ochi, Shinichiro
Tachibana, Ayumi
Yoshida, Taku
Shimizu, Hideaki
Mori, Takaaki
Iga, Jun-ichi
Ueno, Shu-ichi
Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title_full Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title_fullStr Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title_full_unstemmed Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title_short Blood CDKN2A Gene Expression in Aging and Neurodegenerative Diseases
title_sort blood cdkn2a gene expression in aging and neurodegenerative diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461666/
https://www.ncbi.nlm.nih.gov/pubmed/34219731
http://dx.doi.org/10.3233/JAD-210483
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