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Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys

BACKGROUND: Genome-wide association studies have identified more than 60 single nucleotide polymorphisms associated with Body Mass Index (BMI). Additional genetic variants, such as copy number variations (CNV), have also been investigated in relation to BMI. Recently, the highly polymorphic CNV in t...

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Autores principales: Marcovecchio, M. Loredana, Florio, Rosalba, Verginelli, Fabio, De Lellis, Laura, Capelli, Cristian, Verzilli, Delfina, Chiarelli, Francesco, Mohn, Angelika, Cama, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858278/
https://www.ncbi.nlm.nih.gov/pubmed/27149670
http://dx.doi.org/10.1371/journal.pone.0154961
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author Marcovecchio, M. Loredana
Florio, Rosalba
Verginelli, Fabio
De Lellis, Laura
Capelli, Cristian
Verzilli, Delfina
Chiarelli, Francesco
Mohn, Angelika
Cama, Alessandro
author_facet Marcovecchio, M. Loredana
Florio, Rosalba
Verginelli, Fabio
De Lellis, Laura
Capelli, Cristian
Verzilli, Delfina
Chiarelli, Francesco
Mohn, Angelika
Cama, Alessandro
author_sort Marcovecchio, M. Loredana
collection PubMed
description BACKGROUND: Genome-wide association studies have identified more than 60 single nucleotide polymorphisms associated with Body Mass Index (BMI). Additional genetic variants, such as copy number variations (CNV), have also been investigated in relation to BMI. Recently, the highly polymorphic CNV in the salivary amylase (AMY1) gene, encoding an enzyme implicated in the first step of starch digestion, has been associated with obesity in adults and children. We assessed the potential association between AMY1 copy number and a wide range of BMI in a population of Italian school-children. METHODS: 744 children (354 boys, 390 girls, mean age (±SD): 8.4±1.4years) underwent anthropometric assessments (height, weight) and collection of saliva samples for DNA extraction. AMY1 copies were evaluated by quantitative PCR. RESULTS: A significant increase of BMI z-score by decreasing AMY1 copy number was observed in boys (β: -0.117, p = 0.033), but not in girls. Similarly, waist circumference (β: -0.155, p = 0.003, adjusted for age) was negatively influenced by AMY1 copy number in boys. Boys with 8 or more AMY1 copy numbers presented a significant lower BMI z-score (p = 0.04) and waist circumference (p = 0.01) when compared to boys with less than 8 copy numbers. CONCLUSIONS: In this pediatric-only, population-based study, a lower AMY1 copy number emerged to be associated with increased BMI in boys. These data confirm previous findings from adult studies and support a potential role of a higher copy number of the salivary AMY1 gene in protecting from excess weight gain.
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spelling pubmed-48582782016-05-13 Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys Marcovecchio, M. Loredana Florio, Rosalba Verginelli, Fabio De Lellis, Laura Capelli, Cristian Verzilli, Delfina Chiarelli, Francesco Mohn, Angelika Cama, Alessandro PLoS One Research Article BACKGROUND: Genome-wide association studies have identified more than 60 single nucleotide polymorphisms associated with Body Mass Index (BMI). Additional genetic variants, such as copy number variations (CNV), have also been investigated in relation to BMI. Recently, the highly polymorphic CNV in the salivary amylase (AMY1) gene, encoding an enzyme implicated in the first step of starch digestion, has been associated with obesity in adults and children. We assessed the potential association between AMY1 copy number and a wide range of BMI in a population of Italian school-children. METHODS: 744 children (354 boys, 390 girls, mean age (±SD): 8.4±1.4years) underwent anthropometric assessments (height, weight) and collection of saliva samples for DNA extraction. AMY1 copies were evaluated by quantitative PCR. RESULTS: A significant increase of BMI z-score by decreasing AMY1 copy number was observed in boys (β: -0.117, p = 0.033), but not in girls. Similarly, waist circumference (β: -0.155, p = 0.003, adjusted for age) was negatively influenced by AMY1 copy number in boys. Boys with 8 or more AMY1 copy numbers presented a significant lower BMI z-score (p = 0.04) and waist circumference (p = 0.01) when compared to boys with less than 8 copy numbers. CONCLUSIONS: In this pediatric-only, population-based study, a lower AMY1 copy number emerged to be associated with increased BMI in boys. These data confirm previous findings from adult studies and support a potential role of a higher copy number of the salivary AMY1 gene in protecting from excess weight gain. Public Library of Science 2016-05-05 /pmc/articles/PMC4858278/ /pubmed/27149670 http://dx.doi.org/10.1371/journal.pone.0154961 Text en © 2016 Marcovecchio 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
Marcovecchio, M. Loredana
Florio, Rosalba
Verginelli, Fabio
De Lellis, Laura
Capelli, Cristian
Verzilli, Delfina
Chiarelli, Francesco
Mohn, Angelika
Cama, Alessandro
Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title_full Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title_fullStr Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title_full_unstemmed Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title_short Low AMY1 Gene Copy Number Is Associated with Increased Body Mass Index in Prepubertal Boys
title_sort low amy1 gene copy number is associated with increased body mass index in prepubertal boys
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858278/
https://www.ncbi.nlm.nih.gov/pubmed/27149670
http://dx.doi.org/10.1371/journal.pone.0154961
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