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PROP taster status interacts with the built environment to influence children's food acceptance and body weight status

Eating behaviors and obesity are complex phenotypes influenced by genes and access to foods in the environment, but few studies have investigated the interaction of these two variables. The purpose of this study was to use a gene-environment interaction model to test for differences in children'...

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Autores principales: Burd, Carlye, Senerat, Araliya, Chambers, Earle, Keller, Kathleen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661723/
https://www.ncbi.nlm.nih.gov/pubmed/23401219
http://dx.doi.org/10.1002/oby.20059
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author Burd, Carlye
Senerat, Araliya
Chambers, Earle
Keller, Kathleen L.
author_facet Burd, Carlye
Senerat, Araliya
Chambers, Earle
Keller, Kathleen L.
author_sort Burd, Carlye
collection PubMed
description Eating behaviors and obesity are complex phenotypes influenced by genes and access to foods in the environment, but few studies have investigated the interaction of these two variables. The purpose of this study was to use a gene-environment interaction model to test for differences in children's food acceptance and body weights. Inherited ability to taste 6-n-propylthiouracil (PROP) was assessed as a marker of oral taste responsiveness. Food environment was classified as “healthy” or “unhealthy” based on proximity to outlets that sell fruits/vegetables and fast foods using Geographic Information Systems (GIS). The cohort consisted of 120 children, ages 4–6 years, recruited from New York City over 2005–2010. Home address and other demographic variables were reported by parents and PROP status, food acceptance, and anthropometrics were assessed in the laboratory. Based on a screening test, children were classified as PROP tasters or non-tasters. Hierarchical linear models analysis of variance was performed to examine differences in food acceptance and body mass index (BMI) z-scores as a function of PROP status, the food environment (“healthy” vs. “unhealthy”), and their interaction. Results showed an interaction between taster status and the food environment on BMI z-score and food acceptance. Non-taster children living in healthy food environments had greater acceptance of vegetables than taster children living in healthy food environments (p≤0.005). Moreover, non-tasters from unhealthy food environments had higher BMI z-scores than all other groups (p≤0.005). Incorporating genetic markers of taste into studies that assess the built environment may improve the ability of these measures to predict risk for obesity and eating behaviors.
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spelling pubmed-36617232013-10-01 PROP taster status interacts with the built environment to influence children's food acceptance and body weight status Burd, Carlye Senerat, Araliya Chambers, Earle Keller, Kathleen L. Obesity (Silver Spring) Article Eating behaviors and obesity are complex phenotypes influenced by genes and access to foods in the environment, but few studies have investigated the interaction of these two variables. The purpose of this study was to use a gene-environment interaction model to test for differences in children's food acceptance and body weights. Inherited ability to taste 6-n-propylthiouracil (PROP) was assessed as a marker of oral taste responsiveness. Food environment was classified as “healthy” or “unhealthy” based on proximity to outlets that sell fruits/vegetables and fast foods using Geographic Information Systems (GIS). The cohort consisted of 120 children, ages 4–6 years, recruited from New York City over 2005–2010. Home address and other demographic variables were reported by parents and PROP status, food acceptance, and anthropometrics were assessed in the laboratory. Based on a screening test, children were classified as PROP tasters or non-tasters. Hierarchical linear models analysis of variance was performed to examine differences in food acceptance and body mass index (BMI) z-scores as a function of PROP status, the food environment (“healthy” vs. “unhealthy”), and their interaction. Results showed an interaction between taster status and the food environment on BMI z-score and food acceptance. Non-taster children living in healthy food environments had greater acceptance of vegetables than taster children living in healthy food environments (p≤0.005). Moreover, non-tasters from unhealthy food environments had higher BMI z-scores than all other groups (p≤0.005). Incorporating genetic markers of taste into studies that assess the built environment may improve the ability of these measures to predict risk for obesity and eating behaviors. 2012-12-27 2013-04 /pmc/articles/PMC3661723/ /pubmed/23401219 http://dx.doi.org/10.1002/oby.20059 Text en http://www.nature.com/authors/editorial_policies/license.html#terms 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
Burd, Carlye
Senerat, Araliya
Chambers, Earle
Keller, Kathleen L.
PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title_full PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title_fullStr PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title_full_unstemmed PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title_short PROP taster status interacts with the built environment to influence children's food acceptance and body weight status
title_sort prop taster status interacts with the built environment to influence children's food acceptance and body weight status
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661723/
https://www.ncbi.nlm.nih.gov/pubmed/23401219
http://dx.doi.org/10.1002/oby.20059
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