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Aerobic capacity and telomere length in human skeletal muscle and leukocytes across the lifespan
Author(s) -
Danielle Hiam,
Cassandra Smith,
Sarah Voisin,
Joshua Denham,
Xu Yan,
Shanie Landen,
Macsue Jacques,
Javier AlvarezRomero,
Andrew Garnham,
Mary N. Woessner,
Markus Herrmann,
Gustavo Duque,
Itamar Levinger,
Nir Ey
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102627
Subject(s) - telomere , aerobic capacity , skeletal muscle , ageing , aerobic exercise , cohort , sarcopenia , body mass index , medicine , endocrinology , biology , gene , genetics
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.

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