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Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease

INTRODUCTION: The “epigenetic clock” is a DNA methylation–based estimate of biological age and is correlated with chronological age—the greatest risk factor for Alzheimer's disease (AD). Genetic and environmental risk factors exist for AD, several of which are potentially modifiable. In this st...

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Autores principales: McCartney, Daniel L., Stevenson, Anna J., Walker, Rosie M., Gibson, Jude, Morris, Stewart W., Campbell, Archie, Murray, Alison D., Whalley, Heather C., Porteous, David J., McIntosh, Andrew M., Evans, Kathryn L., Deary, Ian J., Marioni, Riccardo E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111045/
https://www.ncbi.nlm.nih.gov/pubmed/30167451
http://dx.doi.org/10.1016/j.dadm.2018.05.006
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author McCartney, Daniel L.
Stevenson, Anna J.
Walker, Rosie M.
Gibson, Jude
Morris, Stewart W.
Campbell, Archie
Murray, Alison D.
Whalley, Heather C.
Porteous, David J.
McIntosh, Andrew M.
Evans, Kathryn L.
Deary, Ian J.
Marioni, Riccardo E.
author_facet McCartney, Daniel L.
Stevenson, Anna J.
Walker, Rosie M.
Gibson, Jude
Morris, Stewart W.
Campbell, Archie
Murray, Alison D.
Whalley, Heather C.
Porteous, David J.
McIntosh, Andrew M.
Evans, Kathryn L.
Deary, Ian J.
Marioni, Riccardo E.
author_sort McCartney, Daniel L.
collection PubMed
description INTRODUCTION: The “epigenetic clock” is a DNA methylation–based estimate of biological age and is correlated with chronological age—the greatest risk factor for Alzheimer's disease (AD). Genetic and environmental risk factors exist for AD, several of which are potentially modifiable. In this study, we assess the relationship between the epigenetic clock and AD risk factors. METHODS: Multilevel models were used to assess the relationship between age acceleration (the residual of biological age regressed onto chronological age) and AD risk factors relating to cognitive reserve, lifestyle, disease, and genetics in the Generation Scotland study (n = 5100). RESULTS: We report significant associations between age acceleration and body mass index, total cholesterol to high-density lipoprotein cholesterol ratios, socioeconomic status, high blood pressure, and smoking behavior (Bonferroni-adjusted P < .05). DISCUSSION: Associations are present between environmental risk factors for AD and age acceleration. Measures to modify such risk factors might improve the risk profile for AD and the rate of biological ageing. Future longitudinal analyses are therefore warranted.
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spelling pubmed-61110452018-08-30 Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease McCartney, Daniel L. Stevenson, Anna J. Walker, Rosie M. Gibson, Jude Morris, Stewart W. Campbell, Archie Murray, Alison D. Whalley, Heather C. Porteous, David J. McIntosh, Andrew M. Evans, Kathryn L. Deary, Ian J. Marioni, Riccardo E. Alzheimers Dement (Amst) Genetics INTRODUCTION: The “epigenetic clock” is a DNA methylation–based estimate of biological age and is correlated with chronological age—the greatest risk factor for Alzheimer's disease (AD). Genetic and environmental risk factors exist for AD, several of which are potentially modifiable. In this study, we assess the relationship between the epigenetic clock and AD risk factors. METHODS: Multilevel models were used to assess the relationship between age acceleration (the residual of biological age regressed onto chronological age) and AD risk factors relating to cognitive reserve, lifestyle, disease, and genetics in the Generation Scotland study (n = 5100). RESULTS: We report significant associations between age acceleration and body mass index, total cholesterol to high-density lipoprotein cholesterol ratios, socioeconomic status, high blood pressure, and smoking behavior (Bonferroni-adjusted P < .05). DISCUSSION: Associations are present between environmental risk factors for AD and age acceleration. Measures to modify such risk factors might improve the risk profile for AD and the rate of biological ageing. Future longitudinal analyses are therefore warranted. Elsevier 2018-06-21 /pmc/articles/PMC6111045/ /pubmed/30167451 http://dx.doi.org/10.1016/j.dadm.2018.05.006 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Genetics
McCartney, Daniel L.
Stevenson, Anna J.
Walker, Rosie M.
Gibson, Jude
Morris, Stewart W.
Campbell, Archie
Murray, Alison D.
Whalley, Heather C.
Porteous, David J.
McIntosh, Andrew M.
Evans, Kathryn L.
Deary, Ian J.
Marioni, Riccardo E.
Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title_full Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title_fullStr Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title_full_unstemmed Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title_short Investigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's disease
title_sort investigating the relationship between dna methylation age acceleration and risk factors for alzheimer's disease
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111045/
https://www.ncbi.nlm.nih.gov/pubmed/30167451
http://dx.doi.org/10.1016/j.dadm.2018.05.006
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