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Biological clocks and physical functioning in monozygotic female twins

BACKGROUND: Biomarkers of biological aging – DNA methylation age (DNAm age) and leukocyte telomere length (LTL)– correlate strongly with chronological age across the life course. It is, however, unclear how these measures of cellular wear and tear are associated with muscle strength and functional c...

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Autores principales: Sillanpää, Elina, Laakkonen, Eija K., Vaara, Elina, Rantanen, Taina, Kovanen, Vuokko, Sipilä, Sarianna, Kaprio, Jaakko, Ollikainen, Miina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883300/
https://www.ncbi.nlm.nih.gov/pubmed/29614968
http://dx.doi.org/10.1186/s12877-018-0775-6
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author Sillanpää, Elina
Laakkonen, Eija K.
Vaara, Elina
Rantanen, Taina
Kovanen, Vuokko
Sipilä, Sarianna
Kaprio, Jaakko
Ollikainen, Miina
author_facet Sillanpää, Elina
Laakkonen, Eija K.
Vaara, Elina
Rantanen, Taina
Kovanen, Vuokko
Sipilä, Sarianna
Kaprio, Jaakko
Ollikainen, Miina
author_sort Sillanpää, Elina
collection PubMed
description BACKGROUND: Biomarkers of biological aging – DNA methylation age (DNAm age) and leukocyte telomere length (LTL)– correlate strongly with chronological age across the life course. It is, however, unclear how these measures of cellular wear and tear are associated with muscle strength and functional capacity, which are known to decline with older age and are associated with mortality. We investigated if DNAm age and LTL were associated with body composition and physical functioning by examining 48 monozygotic twin sisters. METHODS: White blood cell DNAm age (predicted years) was calculated from Illumina 450 k BeadChip methylation data using an online calculator. DNAm age acceleration was defined from the residuals derived from a linear regression model of DNAm age on chronological age. LTL was measured by qPCR. Total body percentage of fat and lean mass were estimated using bioimpedance. Physical functioning was measured by grip strength, knee extension strength and by 10 m maximal walking speed test. RESULTS: In all participants, DNAm age (58.4 ± 6.6) was lower than chronological age (61.3 ± 5.9 years). Pairwise correlations of monozygotic co-twins were high for DNAm age (0.88, 95% CI 0.79, 0.97), age acceleration (0.68, 95% CI 0.30, 0.85) and LTL (0.77, 95% CI 0.60, 0.94). Increased age acceleration i.e. faster epigenetic aging compared to chronological age was associated with lower grip strength (β = − 5.3 SE 1.9 p = 0.011), but not with other measures of physical functioning or body composition. LTL was not associated with body composition or physical functioning. CONCLUSIONS: To conclude, accelerated DNAm age is associated with lower grip strength, a biomarker known to be associated with physiological aging, and which predicts decline in physical functioning and mortality. Further studies may clarify whether epigenetic aging explains the decline in muscle strength with aging or whether DNAm age just illustrates the progress of aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-018-0775-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-58833002018-04-10 Biological clocks and physical functioning in monozygotic female twins Sillanpää, Elina Laakkonen, Eija K. Vaara, Elina Rantanen, Taina Kovanen, Vuokko Sipilä, Sarianna Kaprio, Jaakko Ollikainen, Miina BMC Geriatr Research Article BACKGROUND: Biomarkers of biological aging – DNA methylation age (DNAm age) and leukocyte telomere length (LTL)– correlate strongly with chronological age across the life course. It is, however, unclear how these measures of cellular wear and tear are associated with muscle strength and functional capacity, which are known to decline with older age and are associated with mortality. We investigated if DNAm age and LTL were associated with body composition and physical functioning by examining 48 monozygotic twin sisters. METHODS: White blood cell DNAm age (predicted years) was calculated from Illumina 450 k BeadChip methylation data using an online calculator. DNAm age acceleration was defined from the residuals derived from a linear regression model of DNAm age on chronological age. LTL was measured by qPCR. Total body percentage of fat and lean mass were estimated using bioimpedance. Physical functioning was measured by grip strength, knee extension strength and by 10 m maximal walking speed test. RESULTS: In all participants, DNAm age (58.4 ± 6.6) was lower than chronological age (61.3 ± 5.9 years). Pairwise correlations of monozygotic co-twins were high for DNAm age (0.88, 95% CI 0.79, 0.97), age acceleration (0.68, 95% CI 0.30, 0.85) and LTL (0.77, 95% CI 0.60, 0.94). Increased age acceleration i.e. faster epigenetic aging compared to chronological age was associated with lower grip strength (β = − 5.3 SE 1.9 p = 0.011), but not with other measures of physical functioning or body composition. LTL was not associated with body composition or physical functioning. CONCLUSIONS: To conclude, accelerated DNAm age is associated with lower grip strength, a biomarker known to be associated with physiological aging, and which predicts decline in physical functioning and mortality. Further studies may clarify whether epigenetic aging explains the decline in muscle strength with aging or whether DNAm age just illustrates the progress of aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12877-018-0775-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-04 /pmc/articles/PMC5883300/ /pubmed/29614968 http://dx.doi.org/10.1186/s12877-018-0775-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sillanpää, Elina
Laakkonen, Eija K.
Vaara, Elina
Rantanen, Taina
Kovanen, Vuokko
Sipilä, Sarianna
Kaprio, Jaakko
Ollikainen, Miina
Biological clocks and physical functioning in monozygotic female twins
title Biological clocks and physical functioning in monozygotic female twins
title_full Biological clocks and physical functioning in monozygotic female twins
title_fullStr Biological clocks and physical functioning in monozygotic female twins
title_full_unstemmed Biological clocks and physical functioning in monozygotic female twins
title_short Biological clocks and physical functioning in monozygotic female twins
title_sort biological clocks and physical functioning in monozygotic female twins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883300/
https://www.ncbi.nlm.nih.gov/pubmed/29614968
http://dx.doi.org/10.1186/s12877-018-0775-6
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