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Development of sleep patterns in children with obese and normal‐weight parents

AIM: To study the sleep development and sleep characteristics in children at different obesity risks, based on parental weight, and also to explore their weekday–weekend sleep variations and associated family factors. METHODS: A total of 145 children participating in a longitudinal obesity preventio...

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Autores principales: Xiu, Lijuan, Hagströmer, Maria, Bergqvist‐Norén, Linnea, Johansson, Elin, Ekbom, Kerstin, Svensson, Viktoria, Marcus, Claude, Ekstedt, Mirjam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899924/
https://www.ncbi.nlm.nih.gov/pubmed/30414228
http://dx.doi.org/10.1111/jpc.14294
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author Xiu, Lijuan
Hagströmer, Maria
Bergqvist‐Norén, Linnea
Johansson, Elin
Ekbom, Kerstin
Svensson, Viktoria
Marcus, Claude
Ekstedt, Mirjam
author_facet Xiu, Lijuan
Hagströmer, Maria
Bergqvist‐Norén, Linnea
Johansson, Elin
Ekbom, Kerstin
Svensson, Viktoria
Marcus, Claude
Ekstedt, Mirjam
author_sort Xiu, Lijuan
collection PubMed
description AIM: To study the sleep development and sleep characteristics in children at different obesity risks, based on parental weight, and also to explore their weekday–weekend sleep variations and associated family factors. METHODS: A total of 145 children participating in a longitudinal obesity prevention project were included, of which 37 had normal‐weight parents (low obesity risk), and 108 had overweight/obese parents (high obesity risk). Sleep diaries at ages 1 and 2 years were used to study sleep development in children at different obesity risks. Objectively assessed sleep using an accelerometer at 2 years of age was used to analyse weekday–weekend sleep variations. RESULTS: There was no difference in sleep development from age 1 to age 2 among children at different obesity risks, but more children in the high‐risk group had prolonged sleep onset latency and low sleep efficiency. At 2 years of age, children in the high‐risk group had more weekday–weekend variation in sleep offset (mean difference 18 min, 95% confidence interval (CI) 4–33 min), midpoint of sleep (mean difference 14 min, 95% CI 3–25 min) and nap onset (mean difference 42 min, 95% CI 10–74 min) than children in the low‐risk group, after adjusting for other family factors. However, no difference could be detected between groups in weekday–weekend variation in sleep duration. CONCLUSIONS: Unfavourable sleep characteristics, as well as more variation in sleep schedules, have been observed in children at high obesity risk. While the differences were relatively small, they may reflect the unfavourable sleep hygiene in families at high obesity risk.
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spelling pubmed-68999242019-12-20 Development of sleep patterns in children with obese and normal‐weight parents Xiu, Lijuan Hagströmer, Maria Bergqvist‐Norén, Linnea Johansson, Elin Ekbom, Kerstin Svensson, Viktoria Marcus, Claude Ekstedt, Mirjam J Paediatr Child Health Original Articles AIM: To study the sleep development and sleep characteristics in children at different obesity risks, based on parental weight, and also to explore their weekday–weekend sleep variations and associated family factors. METHODS: A total of 145 children participating in a longitudinal obesity prevention project were included, of which 37 had normal‐weight parents (low obesity risk), and 108 had overweight/obese parents (high obesity risk). Sleep diaries at ages 1 and 2 years were used to study sleep development in children at different obesity risks. Objectively assessed sleep using an accelerometer at 2 years of age was used to analyse weekday–weekend sleep variations. RESULTS: There was no difference in sleep development from age 1 to age 2 among children at different obesity risks, but more children in the high‐risk group had prolonged sleep onset latency and low sleep efficiency. At 2 years of age, children in the high‐risk group had more weekday–weekend variation in sleep offset (mean difference 18 min, 95% confidence interval (CI) 4–33 min), midpoint of sleep (mean difference 14 min, 95% CI 3–25 min) and nap onset (mean difference 42 min, 95% CI 10–74 min) than children in the low‐risk group, after adjusting for other family factors. However, no difference could be detected between groups in weekday–weekend variation in sleep duration. CONCLUSIONS: Unfavourable sleep characteristics, as well as more variation in sleep schedules, have been observed in children at high obesity risk. While the differences were relatively small, they may reflect the unfavourable sleep hygiene in families at high obesity risk. John Wiley & Sons Australia, Ltd 2018-11-10 2019-07 /pmc/articles/PMC6899924/ /pubmed/30414228 http://dx.doi.org/10.1111/jpc.14294 Text en © 2018 The Authors. Journal of Paediatrics and Child Health published by John Wiley & Sons Australia, Ltd on behalf of Paediatrics and Child Health Division (The Royal Australasian College of Physicians) This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Xiu, Lijuan
Hagströmer, Maria
Bergqvist‐Norén, Linnea
Johansson, Elin
Ekbom, Kerstin
Svensson, Viktoria
Marcus, Claude
Ekstedt, Mirjam
Development of sleep patterns in children with obese and normal‐weight parents
title Development of sleep patterns in children with obese and normal‐weight parents
title_full Development of sleep patterns in children with obese and normal‐weight parents
title_fullStr Development of sleep patterns in children with obese and normal‐weight parents
title_full_unstemmed Development of sleep patterns in children with obese and normal‐weight parents
title_short Development of sleep patterns in children with obese and normal‐weight parents
title_sort development of sleep patterns in children with obese and normal‐weight parents
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899924/
https://www.ncbi.nlm.nih.gov/pubmed/30414228
http://dx.doi.org/10.1111/jpc.14294
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