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Leukocyte telomere dynamics in the elderly

Limited data suggest that leukocytes of the elderly display ultra-short telomeres. It was reported that in some elderly persons leukocyte telomere length (LTL) shows age-dependent elongation. Using cross-sectional and longitudinal models, we characterized LTL dynamics in participants of the Longitud...

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Autores principales: Steenstrup, Troels, Hjelmborg, Jacob v. B., Mortensen, Laust H., Kimura, Masayuki, Christensen, Kaare, Aviv, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3604590/
https://www.ncbi.nlm.nih.gov/pubmed/23430034
http://dx.doi.org/10.1007/s10654-013-9780-4
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author Steenstrup, Troels
Hjelmborg, Jacob v. B.
Mortensen, Laust H.
Kimura, Masayuki
Christensen, Kaare
Aviv, Abraham
author_facet Steenstrup, Troels
Hjelmborg, Jacob v. B.
Mortensen, Laust H.
Kimura, Masayuki
Christensen, Kaare
Aviv, Abraham
author_sort Steenstrup, Troels
collection PubMed
description Limited data suggest that leukocytes of the elderly display ultra-short telomeres. It was reported that in some elderly persons leukocyte telomere length (LTL) shows age-dependent elongation. Using cross-sectional and longitudinal models, we characterized LTL dynamics in participants of the Longitudinal Study of Aging Danish Twins. We measured LTL by Southern blots of the terminal restriction fragment length (TRFL) in 476 individuals (73–94 years) in a cross-sectional evaluation and in a subset of this cohort comprising 80 individuals (73–81 years at baseline) who were followed–up for approximately 10 years. Based on the mean TRFL, we found that a) the average rate of LTL attrition was respectively, 27 bp/year (P < 0.001) and 31 bp/year (P < 0.001) for the cross-sectional and longitudinal evaluations, and b) mean TRFL was 180 bp (95 % CI 43, 320) longer in females than males (P < 0.010). For the TRFL distribution, which captures telomeres of all lengths in the DNA sample, we observed significant shifts with age toward shorter telomeres. Based on the measurement error of the TRFLs, we computed that in the longitudinal evaluation 10.6 % of individuals would manifest LTL elongation over 10 years, assuming a 340 bp attrition during this period. This was not significantly different from the empirical observation of 7.5 % of individuals showing LTL elongation. We conclude that accumulation of ultra-short telomeres in leukocytes of the elderly reflects a shift toward shorter telomeres in the entire telomere distribution. Measurement error is the probable explanation for LTL elongation in longitudinal studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10654-013-9780-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-36045902013-03-25 Leukocyte telomere dynamics in the elderly Steenstrup, Troels Hjelmborg, Jacob v. B. Mortensen, Laust H. Kimura, Masayuki Christensen, Kaare Aviv, Abraham Eur J Epidemiol Gerontologic Epidemiology Limited data suggest that leukocytes of the elderly display ultra-short telomeres. It was reported that in some elderly persons leukocyte telomere length (LTL) shows age-dependent elongation. Using cross-sectional and longitudinal models, we characterized LTL dynamics in participants of the Longitudinal Study of Aging Danish Twins. We measured LTL by Southern blots of the terminal restriction fragment length (TRFL) in 476 individuals (73–94 years) in a cross-sectional evaluation and in a subset of this cohort comprising 80 individuals (73–81 years at baseline) who were followed–up for approximately 10 years. Based on the mean TRFL, we found that a) the average rate of LTL attrition was respectively, 27 bp/year (P < 0.001) and 31 bp/year (P < 0.001) for the cross-sectional and longitudinal evaluations, and b) mean TRFL was 180 bp (95 % CI 43, 320) longer in females than males (P < 0.010). For the TRFL distribution, which captures telomeres of all lengths in the DNA sample, we observed significant shifts with age toward shorter telomeres. Based on the measurement error of the TRFLs, we computed that in the longitudinal evaluation 10.6 % of individuals would manifest LTL elongation over 10 years, assuming a 340 bp attrition during this period. This was not significantly different from the empirical observation of 7.5 % of individuals showing LTL elongation. We conclude that accumulation of ultra-short telomeres in leukocytes of the elderly reflects a shift toward shorter telomeres in the entire telomere distribution. Measurement error is the probable explanation for LTL elongation in longitudinal studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10654-013-9780-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2013-02-21 2013 /pmc/articles/PMC3604590/ /pubmed/23430034 http://dx.doi.org/10.1007/s10654-013-9780-4 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Gerontologic Epidemiology
Steenstrup, Troels
Hjelmborg, Jacob v. B.
Mortensen, Laust H.
Kimura, Masayuki
Christensen, Kaare
Aviv, Abraham
Leukocyte telomere dynamics in the elderly
title Leukocyte telomere dynamics in the elderly
title_full Leukocyte telomere dynamics in the elderly
title_fullStr Leukocyte telomere dynamics in the elderly
title_full_unstemmed Leukocyte telomere dynamics in the elderly
title_short Leukocyte telomere dynamics in the elderly
title_sort leukocyte telomere dynamics in the elderly
topic Gerontologic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3604590/
https://www.ncbi.nlm.nih.gov/pubmed/23430034
http://dx.doi.org/10.1007/s10654-013-9780-4
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