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Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan
A reduction in aerobic capacity and the shortening of telomeres are hallmarks of the ageing process. We examined whether a lower aerobic capacity is associated with shorter TL in skeletal muscle and/or leukocytes, across a wide age range of individuals. We also tested whether TL in human skeletal mu...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977669/ https://www.ncbi.nlm.nih.gov/pubmed/31901896 http://dx.doi.org/10.18632/aging.102627 |
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author | Hiam, Danielle Smith, Cassandra Voisin, Sarah Denham, Josh Yan, Xu Landen, Shanie Jacques, Macsue Alvarez-Romero, Javier Garnham, Andrew Woessner, Mary N. Herrmann, Markus Duque, Gustavo Levinger, Itamar Eynon, Nir |
author_facet | Hiam, Danielle Smith, Cassandra Voisin, Sarah Denham, Josh Yan, Xu Landen, Shanie Jacques, Macsue Alvarez-Romero, Javier Garnham, Andrew Woessner, Mary N. Herrmann, Markus Duque, Gustavo Levinger, Itamar Eynon, Nir |
author_sort | Hiam, Danielle |
collection | PubMed |
description | A reduction in aerobic capacity and the shortening of telomeres are hallmarks of the ageing process. We examined whether a lower aerobic capacity is associated with shorter TL in skeletal muscle and/or leukocytes, across a wide age range of individuals. We also tested whether TL in human skeletal muscle (MTL) correlates with TL in leukocytes (LTL). Eighty-two recreationally active, healthy men from the Gene SMART cohort (31.4±8.2 years; body mass index (BMI)=25.3±3.3kg/m(2)), and 11 community dwelling older men (74.2±7.5years-old; BMI=28.7±2.8kg/m(2)) participated in the study. Leukocytes and skeletal muscle samples were collected at rest. Relative telomere length (T/S ratio) was measured by RT-PCR. Associations between TL, aerobic capacity (VO(2) peak and peak power) and age were assessed with robust linear models. Older age was associated with shorter LTL (45% variance explained, P<0.001), but not MTL (P= 0.7). Aerobic capacity was not associated with MTL (P=0.5), nor LTL (P=0.3). MTL and LTL were correlated across the lifespan (r(s)=0.26, P=0.03). In healthy individuals, age explain most of the variability of LTL and this appears to be independent of individual aerobic capacity. Individuals with longer LTL also have a longer MTL, suggesting that there might be a shared molecular mechanism regulating telomere length. |
format | Online Article Text |
id | pubmed-6977669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-69776692020-01-31 Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan Hiam, Danielle Smith, Cassandra Voisin, Sarah Denham, Josh Yan, Xu Landen, Shanie Jacques, Macsue Alvarez-Romero, Javier Garnham, Andrew Woessner, Mary N. Herrmann, Markus Duque, Gustavo Levinger, Itamar Eynon, Nir Aging (Albany NY) Research Paper A reduction in aerobic capacity and the shortening of telomeres are hallmarks of the ageing process. We examined whether a lower aerobic capacity is associated with shorter TL in skeletal muscle and/or leukocytes, across a wide age range of individuals. We also tested whether TL in human skeletal muscle (MTL) correlates with TL in leukocytes (LTL). Eighty-two recreationally active, healthy men from the Gene SMART cohort (31.4±8.2 years; body mass index (BMI)=25.3±3.3kg/m(2)), and 11 community dwelling older men (74.2±7.5years-old; BMI=28.7±2.8kg/m(2)) participated in the study. Leukocytes and skeletal muscle samples were collected at rest. Relative telomere length (T/S ratio) was measured by RT-PCR. Associations between TL, aerobic capacity (VO(2) peak and peak power) and age were assessed with robust linear models. Older age was associated with shorter LTL (45% variance explained, P<0.001), but not MTL (P= 0.7). Aerobic capacity was not associated with MTL (P=0.5), nor LTL (P=0.3). MTL and LTL were correlated across the lifespan (r(s)=0.26, P=0.03). In healthy individuals, age explain most of the variability of LTL and this appears to be independent of individual aerobic capacity. Individuals with longer LTL also have a longer MTL, suggesting that there might be a shared molecular mechanism regulating telomere length. Impact Journals 2020-01-03 /pmc/articles/PMC6977669/ /pubmed/31901896 http://dx.doi.org/10.18632/aging.102627 Text en Copyright © 2020 Hiam et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Hiam, Danielle Smith, Cassandra Voisin, Sarah Denham, Josh Yan, Xu Landen, Shanie Jacques, Macsue Alvarez-Romero, Javier Garnham, Andrew Woessner, Mary N. Herrmann, Markus Duque, Gustavo Levinger, Itamar Eynon, Nir Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title | Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title_full | Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title_fullStr | Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title_full_unstemmed | Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title_short | Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
title_sort | aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977669/ https://www.ncbi.nlm.nih.gov/pubmed/31901896 http://dx.doi.org/10.18632/aging.102627 |
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