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Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children
Disruption of circadian rhythms and variations in the FTO gene may interfere with energy homeostasis and play a role in the development of obesity. The current study assessed the association of common polymorphisms in the CLOCK and FTO genes with standardized body mass index scores (BMI z-scores) an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423126/ https://www.ncbi.nlm.nih.gov/pubmed/32785234 http://dx.doi.org/10.1371/journal.pone.0236991 |
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author | Meng, Ying Lohse, Barbara Cunningham-Sabo, Leslie |
author_facet | Meng, Ying Lohse, Barbara Cunningham-Sabo, Leslie |
author_sort | Meng, Ying |
collection | PubMed |
description | Disruption of circadian rhythms and variations in the FTO gene may interfere with energy homeostasis and play a role in the development of obesity. The current study assessed the association of common polymorphisms in the CLOCK and FTO genes with standardized body mass index scores (BMI z-scores) and their potential modification of the impact of a culinary nutrition and physical activity intervention in school-age children. Anthropometric measurements were collected in 121 children at the baseline and one-year follow-up of a controlled trial of a school-based culinary nutrition and physical activity intervention. Genotypes of the CLOCK polymorphism (rs1801260) and the FTO polymorphism (rs9939609) were obtained from buccal swabs. Linear mixed-effects regression was applied to evaluate the genetic association and adjust for clusters within families and schools. In our participants, obesity affected 6.6% (8/121) of the children at the baseline and 6.4% (7/109) of the children at the follow-up. The associations between the age- and sex-adjusted BMI z-scores and the two polymorphisms did not reach statistically significance. Yet, sex potentially modified the association between rs1801260 and BMI z-scores. In girls, the G allele carriers had a higher BMI z-scores at the baseline and the follow-up. These polymorphisms did not modify the effect of our culinary nutrition and physical activity intervention on BMI z-scores. Sex is a potential modifier for the association between the CLOCK polymorphism, rs1801260, and BMI z-scores in school-age children. Further investigation is warranted to delineate the sex-dependent role of the CLOCK polymorphisms in the development of childhood obesity. |
format | Online Article Text |
id | pubmed-7423126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74231262020-08-20 Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children Meng, Ying Lohse, Barbara Cunningham-Sabo, Leslie PLoS One Research Article Disruption of circadian rhythms and variations in the FTO gene may interfere with energy homeostasis and play a role in the development of obesity. The current study assessed the association of common polymorphisms in the CLOCK and FTO genes with standardized body mass index scores (BMI z-scores) and their potential modification of the impact of a culinary nutrition and physical activity intervention in school-age children. Anthropometric measurements were collected in 121 children at the baseline and one-year follow-up of a controlled trial of a school-based culinary nutrition and physical activity intervention. Genotypes of the CLOCK polymorphism (rs1801260) and the FTO polymorphism (rs9939609) were obtained from buccal swabs. Linear mixed-effects regression was applied to evaluate the genetic association and adjust for clusters within families and schools. In our participants, obesity affected 6.6% (8/121) of the children at the baseline and 6.4% (7/109) of the children at the follow-up. The associations between the age- and sex-adjusted BMI z-scores and the two polymorphisms did not reach statistically significance. Yet, sex potentially modified the association between rs1801260 and BMI z-scores. In girls, the G allele carriers had a higher BMI z-scores at the baseline and the follow-up. These polymorphisms did not modify the effect of our culinary nutrition and physical activity intervention on BMI z-scores. Sex is a potential modifier for the association between the CLOCK polymorphism, rs1801260, and BMI z-scores in school-age children. Further investigation is warranted to delineate the sex-dependent role of the CLOCK polymorphisms in the development of childhood obesity. Public Library of Science 2020-08-12 /pmc/articles/PMC7423126/ /pubmed/32785234 http://dx.doi.org/10.1371/journal.pone.0236991 Text en © 2020 Meng et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Meng, Ying Lohse, Barbara Cunningham-Sabo, Leslie Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title | Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title_full | Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title_fullStr | Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title_full_unstemmed | Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title_short | Sex modifies the association between the CLOCK variant rs1801260 and BMI in school-age children |
title_sort | sex modifies the association between the clock variant rs1801260 and bmi in school-age children |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423126/ https://www.ncbi.nlm.nih.gov/pubmed/32785234 http://dx.doi.org/10.1371/journal.pone.0236991 |
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