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Telomere length and reproductive aging

BACKGROUND: Rate of reproductive aging may be related to rate of biological aging. Thus, indicators of aging, such as short telomere length, may be more frequent in women with a history suggestive of premature reproductive senescence. METHODS: Telomere-specific quantitative PCR was used to assess te...

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Autores principales: Hanna, Courtney W., Bretherick, Karla L., Gair, Jane L., Fluker, Margo R., Stephenson, Mary D., Robinson, Wendy P.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667790/
https://www.ncbi.nlm.nih.gov/pubmed/19202142
http://dx.doi.org/10.1093/humrep/dep007
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author Hanna, Courtney W.
Bretherick, Karla L.
Gair, Jane L.
Fluker, Margo R.
Stephenson, Mary D.
Robinson, Wendy P.
author_facet Hanna, Courtney W.
Bretherick, Karla L.
Gair, Jane L.
Fluker, Margo R.
Stephenson, Mary D.
Robinson, Wendy P.
author_sort Hanna, Courtney W.
collection PubMed
description BACKGROUND: Rate of reproductive aging may be related to rate of biological aging. Thus, indicators of aging, such as short telomere length, may be more frequent in women with a history suggestive of premature reproductive senescence. METHODS: Telomere-specific quantitative PCR was used to assess telomere length in two groups of women with evidence of reproductive aging: (i) patients with idiopathic premature ovarian failure (POF, N = 34) and (ii) women with a history of recurrent miscarriage (RM, N = 95); and two control groups: (1) women from the general population (C1, N = 108) and (2) women who had a healthy pregnancy after 37 years of age (C2, N = 46). RESULTS: The RM group had shorter age-adjusted mean telomere length than controls (8.46 versus 8.92 kb in C1 and 9.11 kb in C2, P = 0.0004 and P = 0.02 for C1 and C2, respectively), although short telomeres were not confined to subsets of this group known to have experienced single or multiple trisomic pregnancies. Although sample size is limited, mean telomere length in the POF group was significantly longer than that in C1 (9.58 versus 8.92 kb, P = 0.01). CONCLUSIONS: Women experiencing RM may have shorter telomeres as a consequence of a more rapid rate of aging, or as a reflection of an increased level of cellular stress. Longer telomere length in the POF group may be explained by abnormal hormone exposure, slow cell division rates or autoimmunity in these women. Despite small sample sizes, these results suggest that different manifestations of reproductive aging are likely influenced by distinct physiological factors.
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spelling pubmed-26677902009-04-13 Telomere length and reproductive aging Hanna, Courtney W. Bretherick, Karla L. Gair, Jane L. Fluker, Margo R. Stephenson, Mary D. Robinson, Wendy P. Hum Reprod Original Articles BACKGROUND: Rate of reproductive aging may be related to rate of biological aging. Thus, indicators of aging, such as short telomere length, may be more frequent in women with a history suggestive of premature reproductive senescence. METHODS: Telomere-specific quantitative PCR was used to assess telomere length in two groups of women with evidence of reproductive aging: (i) patients with idiopathic premature ovarian failure (POF, N = 34) and (ii) women with a history of recurrent miscarriage (RM, N = 95); and two control groups: (1) women from the general population (C1, N = 108) and (2) women who had a healthy pregnancy after 37 years of age (C2, N = 46). RESULTS: The RM group had shorter age-adjusted mean telomere length than controls (8.46 versus 8.92 kb in C1 and 9.11 kb in C2, P = 0.0004 and P = 0.02 for C1 and C2, respectively), although short telomeres were not confined to subsets of this group known to have experienced single or multiple trisomic pregnancies. Although sample size is limited, mean telomere length in the POF group was significantly longer than that in C1 (9.58 versus 8.92 kb, P = 0.01). CONCLUSIONS: Women experiencing RM may have shorter telomeres as a consequence of a more rapid rate of aging, or as a reflection of an increased level of cellular stress. Longer telomere length in the POF group may be explained by abnormal hormone exposure, slow cell division rates or autoimmunity in these women. Despite small sample sizes, these results suggest that different manifestations of reproductive aging are likely influenced by distinct physiological factors. Oxford University Press 2009-05 2009-02-06 /pmc/articles/PMC2667790/ /pubmed/19202142 http://dx.doi.org/10.1093/humrep/dep007 Text en © The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
spellingShingle Original Articles
Hanna, Courtney W.
Bretherick, Karla L.
Gair, Jane L.
Fluker, Margo R.
Stephenson, Mary D.
Robinson, Wendy P.
Telomere length and reproductive aging
title Telomere length and reproductive aging
title_full Telomere length and reproductive aging
title_fullStr Telomere length and reproductive aging
title_full_unstemmed Telomere length and reproductive aging
title_short Telomere length and reproductive aging
title_sort telomere length and reproductive aging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667790/
https://www.ncbi.nlm.nih.gov/pubmed/19202142
http://dx.doi.org/10.1093/humrep/dep007
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