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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2013
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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. |
format | Online Article Text |
id | pubmed-3604590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
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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