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Leukocyte telomere length dynamics in women and men: menopause vs age effects

Background: A longer leukocyte telomere length (LTL) in women than men has been attributed to a slow rate of LTL attrition in women, perhaps due to high estrogen exposure during the premenopausal period. Methods: To test this premise we performed a longitudinal study (an average follow-up of 12 year...

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Autores principales: Dalgård, Christine, Benetos, Athanase, Verhulst, Simon, Labat, Carlos, Kark, Jeremy D, Christensen, Kaare, Kimura, Masayuki, Kyvik, Kirsten Ohm, Aviv, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681111/
https://www.ncbi.nlm.nih.gov/pubmed/26385867
http://dx.doi.org/10.1093/ije/dyv165
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author Dalgård, Christine
Benetos, Athanase
Verhulst, Simon
Labat, Carlos
Kark, Jeremy D
Christensen, Kaare
Kimura, Masayuki
Kyvik, Kirsten Ohm
Aviv, Abraham
author_facet Dalgård, Christine
Benetos, Athanase
Verhulst, Simon
Labat, Carlos
Kark, Jeremy D
Christensen, Kaare
Kimura, Masayuki
Kyvik, Kirsten Ohm
Aviv, Abraham
author_sort Dalgård, Christine
collection PubMed
description Background: A longer leukocyte telomere length (LTL) in women than men has been attributed to a slow rate of LTL attrition in women, perhaps due to high estrogen exposure during the premenopausal period. Methods: To test this premise we performed a longitudinal study (an average follow-up of 12 years) in a subset of the population-based Danish National Twin Registry. Participants consisted of 405 women, aged 37.5 (range 18.0–64.3) years, and 329 men, aged 38.8 (range 18.0–58.5) years, at baseline examination. Results: Women showed a longer LTL [kb ± standard error(SE)] than men (baseline: 7.01 ± 0.03 vs 6.87 ± 0.04; follow-up: 6.79 ± 0.03 vs 6.65 ± 0.03; both P = 0.005). Women displayed deceleration of LTL attrition (bp/years ± SE), as they transitioned from the premenopausal period (20.6 ± 1.0) through the perimenopausal period (16.5 ± 1.3) to the postmenopausal period (15.1 ± 1.7). Age was not associated with LTL attrition in women after statistical control for menopausal status. Men, in contrast, displayed a trend for age-dependent increase in the rate of LTL attrition, which differed significantly from the pattern in women (P for interaction = 0.01). Conclusions: Results indicate that the premenopausal period is expressed in a higher rate of LTL attrition than the postmenopausal period. They further suggest that the sex gap in LTL stems from earlier ages—the period of growth and development. The higher rate of LTL attrition in premenopausal women, we propose, might relate to estrogen-mediated increased turnover of erythrocytes, menstrual bleeding or both.
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spelling pubmed-46811112015-12-16 Leukocyte telomere length dynamics in women and men: menopause vs age effects Dalgård, Christine Benetos, Athanase Verhulst, Simon Labat, Carlos Kark, Jeremy D Christensen, Kaare Kimura, Masayuki Kyvik, Kirsten Ohm Aviv, Abraham Int J Epidemiol Methodology Background: A longer leukocyte telomere length (LTL) in women than men has been attributed to a slow rate of LTL attrition in women, perhaps due to high estrogen exposure during the premenopausal period. Methods: To test this premise we performed a longitudinal study (an average follow-up of 12 years) in a subset of the population-based Danish National Twin Registry. Participants consisted of 405 women, aged 37.5 (range 18.0–64.3) years, and 329 men, aged 38.8 (range 18.0–58.5) years, at baseline examination. Results: Women showed a longer LTL [kb ± standard error(SE)] than men (baseline: 7.01 ± 0.03 vs 6.87 ± 0.04; follow-up: 6.79 ± 0.03 vs 6.65 ± 0.03; both P = 0.005). Women displayed deceleration of LTL attrition (bp/years ± SE), as they transitioned from the premenopausal period (20.6 ± 1.0) through the perimenopausal period (16.5 ± 1.3) to the postmenopausal period (15.1 ± 1.7). Age was not associated with LTL attrition in women after statistical control for menopausal status. Men, in contrast, displayed a trend for age-dependent increase in the rate of LTL attrition, which differed significantly from the pattern in women (P for interaction = 0.01). Conclusions: Results indicate that the premenopausal period is expressed in a higher rate of LTL attrition than the postmenopausal period. They further suggest that the sex gap in LTL stems from earlier ages—the period of growth and development. The higher rate of LTL attrition in premenopausal women, we propose, might relate to estrogen-mediated increased turnover of erythrocytes, menstrual bleeding or both. Oxford University Press 2015-10 2015-09-18 /pmc/articles/PMC4681111/ /pubmed/26385867 http://dx.doi.org/10.1093/ije/dyv165 Text en © The Author 2015. Published by Oxford University Press on behalf of the International Epidemiological Association http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Dalgård, Christine
Benetos, Athanase
Verhulst, Simon
Labat, Carlos
Kark, Jeremy D
Christensen, Kaare
Kimura, Masayuki
Kyvik, Kirsten Ohm
Aviv, Abraham
Leukocyte telomere length dynamics in women and men: menopause vs age effects
title Leukocyte telomere length dynamics in women and men: menopause vs age effects
title_full Leukocyte telomere length dynamics in women and men: menopause vs age effects
title_fullStr Leukocyte telomere length dynamics in women and men: menopause vs age effects
title_full_unstemmed Leukocyte telomere length dynamics in women and men: menopause vs age effects
title_short Leukocyte telomere length dynamics in women and men: menopause vs age effects
title_sort leukocyte telomere length dynamics in women and men: menopause vs age effects
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681111/
https://www.ncbi.nlm.nih.gov/pubmed/26385867
http://dx.doi.org/10.1093/ije/dyv165
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