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Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children

BACKGROUND/OBJECTIVES: Associations between overweight and altered stress biology have been reported cross-sectionally during childhood, but it is unclear whether overweight precedes altered stress biology or if altered stress biology predicts greater likelihood of overweight over time. The current...

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Autores principales: Doom, Jenalee R., Lumeng, Julie C., Sturza, Julie, Kaciroti, Niko, Vazquez, Delia M., Miller, Alison L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050333/
https://www.ncbi.nlm.nih.gov/pubmed/31477784
http://dx.doi.org/10.1038/s41366-019-0447-4
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author Doom, Jenalee R.
Lumeng, Julie C.
Sturza, Julie
Kaciroti, Niko
Vazquez, Delia M.
Miller, Alison L.
author_facet Doom, Jenalee R.
Lumeng, Julie C.
Sturza, Julie
Kaciroti, Niko
Vazquez, Delia M.
Miller, Alison L.
author_sort Doom, Jenalee R.
collection PubMed
description BACKGROUND/OBJECTIVES: Associations between overweight and altered stress biology have been reported cross-sectionally during childhood, but it is unclear whether overweight precedes altered stress biology or if altered stress biology predicts greater likelihood of overweight over time. The current longitudinal study investigates associations between overweight/obesity, salivary alpha amylase and cortisol morning intercept, diurnal slope, and reactivity to social stress in a cohort of low-income children during preschool and middle childhood. SUBJECTS/METHODS: Children were recruited through Head Start and were observed and followed into middle childhood (N = 257; M = 8.0 years). Height and weight were measured at both time points. Saliva samples were collected across the day and in response to a social challenge at both ages for alpha amylase and cortisol determination. RESULTS: Cross-lagged panel analyses indicated that overweight/obesity at preschool predicted lower morning alpha amylase (β = −0.18, 95% CI: −0.34, −0.03; p = .023), lower morning cortisol (β = −0.22, 95% CI: −0.38, −0.06; p = .006), lower sAA diurnal slope (β = −0.18, 95% CI: −0.34, −0.03; p = .021), and lower cortisol stress reactivity (β = −0.19, 95% CI: −0.35, −0.02; p = .031) in middle childhood. Lower alpha amylase reactivity at preschool was the only biological factor that predicted higher likelihood of overweight/obesity at middle childhood (β = −0.20, 95% CI: −0.38, −0.01; p = .035). CONCLUSIONS: These findings suggest that overweight/obesity may be driving changes in stress biology across early to middle childhood, particularly in down-regulation of morning levels of stress hormones, diurnal sAA slope, and cortisol reactivity to stress, rather than stress biology driving overweight/obesity.
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spelling pubmed-70503332020-03-02 Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children Doom, Jenalee R. Lumeng, Julie C. Sturza, Julie Kaciroti, Niko Vazquez, Delia M. Miller, Alison L. Int J Obes (Lond) Article BACKGROUND/OBJECTIVES: Associations between overweight and altered stress biology have been reported cross-sectionally during childhood, but it is unclear whether overweight precedes altered stress biology or if altered stress biology predicts greater likelihood of overweight over time. The current longitudinal study investigates associations between overweight/obesity, salivary alpha amylase and cortisol morning intercept, diurnal slope, and reactivity to social stress in a cohort of low-income children during preschool and middle childhood. SUBJECTS/METHODS: Children were recruited through Head Start and were observed and followed into middle childhood (N = 257; M = 8.0 years). Height and weight were measured at both time points. Saliva samples were collected across the day and in response to a social challenge at both ages for alpha amylase and cortisol determination. RESULTS: Cross-lagged panel analyses indicated that overweight/obesity at preschool predicted lower morning alpha amylase (β = −0.18, 95% CI: −0.34, −0.03; p = .023), lower morning cortisol (β = −0.22, 95% CI: −0.38, −0.06; p = .006), lower sAA diurnal slope (β = −0.18, 95% CI: −0.34, −0.03; p = .021), and lower cortisol stress reactivity (β = −0.19, 95% CI: −0.35, −0.02; p = .031) in middle childhood. Lower alpha amylase reactivity at preschool was the only biological factor that predicted higher likelihood of overweight/obesity at middle childhood (β = −0.20, 95% CI: −0.38, −0.01; p = .035). CONCLUSIONS: These findings suggest that overweight/obesity may be driving changes in stress biology across early to middle childhood, particularly in down-regulation of morning levels of stress hormones, diurnal sAA slope, and cortisol reactivity to stress, rather than stress biology driving overweight/obesity. 2019-09-02 2020-03 /pmc/articles/PMC7050333/ /pubmed/31477784 http://dx.doi.org/10.1038/s41366-019-0447-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Doom, Jenalee R.
Lumeng, Julie C.
Sturza, Julie
Kaciroti, Niko
Vazquez, Delia M.
Miller, Alison L.
Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title_full Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title_fullStr Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title_full_unstemmed Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title_short Longitudinal Associations between Overweight/Obesity and Stress Biology in Low-Income Children
title_sort longitudinal associations between overweight/obesity and stress biology in low-income children
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050333/
https://www.ncbi.nlm.nih.gov/pubmed/31477784
http://dx.doi.org/10.1038/s41366-019-0447-4
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