Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.

Psychological challenges, including traumatic events, have been hypothesized to increase the age-related pace of biological aging. Here we test the hypothesis that psychological challenges can affect the pace of telomere attrition, a marker of cellular aging, using data from an ongoing longitudinal-...

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Main Authors: Cindy K Barha, Katrina G Salvante, Courtney W Hanna, Samantha L Wilson, Wendy P Robinson, Rachel M Altman, Pablo A Nepomnaschy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5444612?pdf=render
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spelling doaj-821262fca76046f399dc5f69c5b9208d2020-11-25T01:46:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01125e017786910.1371/journal.pone.0177869Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.Cindy K BarhaKatrina G SalvanteCourtney W HannaSamantha L WilsonWendy P RobinsonRachel M AltmanPablo A NepomnaschyPsychological challenges, including traumatic events, have been hypothesized to increase the age-related pace of biological aging. Here we test the hypothesis that psychological challenges can affect the pace of telomere attrition, a marker of cellular aging, using data from an ongoing longitudinal-cohort study of Kaqchikel Mayan women living in a population with a high frequency of child mortality, a traumatic life event. Specifically, we evaluate the associations between child mortality, maternal telomere length and the mothers' hypothalamic-pituitary-adrenal axis (HPAA), or stress axis, activity. Child mortality data were collected in 2000 and 2013. HPAA activity was assessed by quantifying cortisol levels in first morning urinary specimens collected every other day for seven weeks in 2013. Telomere length (TL) was quantified using qPCR in 55 women from buccal specimens collected in 2013.Shorter TL with increasing age was only observed in women who experienced child mortality (p = 0.015). Women with higher average basal cortisol (p = 0.007) and greater within-individual variation (standard deviation) in basal cortisol (p = 0.053) presented shorter TL. Non-parametric bootstrapping to estimate mediation effects suggests that HPAA activity mediates the effect of child mortality on TL. Our results are, thus, consistent with the hypothesis that traumatic events can influence cellular aging and that HPAA activity may play a mediatory role. Future large-scale longitudinal studies are necessary to confirm our results and further explore the role of the HPAA in cellular aging, as well as to advance our understanding of the underlying mechanisms involved.http://europepmc.org/articles/PMC5444612?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Cindy K Barha
Katrina G Salvante
Courtney W Hanna
Samantha L Wilson
Wendy P Robinson
Rachel M Altman
Pablo A Nepomnaschy
spellingShingle Cindy K Barha
Katrina G Salvante
Courtney W Hanna
Samantha L Wilson
Wendy P Robinson
Rachel M Altman
Pablo A Nepomnaschy
Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
PLoS ONE
author_facet Cindy K Barha
Katrina G Salvante
Courtney W Hanna
Samantha L Wilson
Wendy P Robinson
Rachel M Altman
Pablo A Nepomnaschy
author_sort Cindy K Barha
title Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
title_short Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
title_full Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
title_fullStr Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
title_full_unstemmed Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
title_sort child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Psychological challenges, including traumatic events, have been hypothesized to increase the age-related pace of biological aging. Here we test the hypothesis that psychological challenges can affect the pace of telomere attrition, a marker of cellular aging, using data from an ongoing longitudinal-cohort study of Kaqchikel Mayan women living in a population with a high frequency of child mortality, a traumatic life event. Specifically, we evaluate the associations between child mortality, maternal telomere length and the mothers' hypothalamic-pituitary-adrenal axis (HPAA), or stress axis, activity. Child mortality data were collected in 2000 and 2013. HPAA activity was assessed by quantifying cortisol levels in first morning urinary specimens collected every other day for seven weeks in 2013. Telomere length (TL) was quantified using qPCR in 55 women from buccal specimens collected in 2013.Shorter TL with increasing age was only observed in women who experienced child mortality (p = 0.015). Women with higher average basal cortisol (p = 0.007) and greater within-individual variation (standard deviation) in basal cortisol (p = 0.053) presented shorter TL. Non-parametric bootstrapping to estimate mediation effects suggests that HPAA activity mediates the effect of child mortality on TL. Our results are, thus, consistent with the hypothesis that traumatic events can influence cellular aging and that HPAA activity may play a mediatory role. Future large-scale longitudinal studies are necessary to confirm our results and further explore the role of the HPAA in cellular aging, as well as to advance our understanding of the underlying mechanisms involved.
url http://europepmc.org/articles/PMC5444612?pdf=render
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