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INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men

BACKGROUND: A common SNP upstream of the INSIG2 gene, rs7566605 (g.-10,1025G>C, Chr2:118,552,255, NT_022135.15), was reported to be associated with obesity (Body Mass Index, [BMI]) in a genome-wide association scan using the Framingham Heart Study but has not been reproduced in other cohorts. As...

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Autores principales: Orkunoglu-Suer, Funda E, Gordish-Dressman, Heather, Clarkson, Priscilla M, Thompson, Paul D, Angelopoulos, Theodore J, Gordon, Paul M, Moyna, Niall M, Pescatello, Linda S, Visich, Paul S, Zoeller, Robert F, Harmon, Brennan, Seip, Richard L, Hoffman, Eric P, Devaney, Joseph M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646703/
https://www.ncbi.nlm.nih.gov/pubmed/19105843
http://dx.doi.org/10.1186/1471-2350-9-117
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author Orkunoglu-Suer, Funda E
Gordish-Dressman, Heather
Clarkson, Priscilla M
Thompson, Paul D
Angelopoulos, Theodore J
Gordon, Paul M
Moyna, Niall M
Pescatello, Linda S
Visich, Paul S
Zoeller, Robert F
Harmon, Brennan
Seip, Richard L
Hoffman, Eric P
Devaney, Joseph M
author_facet Orkunoglu-Suer, Funda E
Gordish-Dressman, Heather
Clarkson, Priscilla M
Thompson, Paul D
Angelopoulos, Theodore J
Gordon, Paul M
Moyna, Niall M
Pescatello, Linda S
Visich, Paul S
Zoeller, Robert F
Harmon, Brennan
Seip, Richard L
Hoffman, Eric P
Devaney, Joseph M
author_sort Orkunoglu-Suer, Funda E
collection PubMed
description BACKGROUND: A common SNP upstream of the INSIG2 gene, rs7566605 (g.-10,1025G>C, Chr2:118,552,255, NT_022135.15), was reported to be associated with obesity (Body Mass Index, [BMI]) in a genome-wide association scan using the Framingham Heart Study but has not been reproduced in other cohorts. As BMI is a relatively insensitive measure of adiposity that is subject to many confounding variables, we sought to determine the relationship between the INSIG2 SNP and subcutaneous fat volumes measured by MRI in a young adult population. METHODS: We genotyped the INSIG2 SNP rs7566605 in college-aged population enrolled in a controlled resistance-training program, (the Functional Polymorphism Associated with Human Muscle Size and Strength, FAMuSS cohort, n = 752 volunteers 18–40 yrs). In this longitudinal study, we examined the effect of the INSIG2 polymorphism on subcutaneous fat and muscle volumes of the upper arm measured by magnetic resonance imaging (MRI) before and after 12 wks of resistance training. Gene/phenotype associations were tested using an analysis of covariance model with age and weight as covariates. Further, the % variation in each phenotype attributable to genotype was determined using hierarchical models and tested with a likelihood ratio test. RESULTS: Women with a copy of the C allele had higher levels of baseline subcutaneous fat (GG: n = 139; 243473 ± 5713 mm(3 )vs. GC/CC: n = 181; 268521 ± 5003 mm(3); p = 0.0011); but men did not show any such association. Men homozygous for the G ancestral allele showed a loss of subcutaneous fat, while those with one or two copies of the C allele gained a greater percentage of subcutaneous fat with resistance training (GG: n = 103; 1.02% ± 1.74% vs. GC/CC: n = 93; 6.39% ± 1.82%; p = 0.035). CONCLUSION: Our results show that the INSIG2 rs7566605 polymorphism underlies variation in subcutaneous adiposity in young adult women and suppresses the positive effects of resistance training on men. This supports and extends the original finding that there is an association between measures of obesity and INSIG2 rs7566605 and further implicates this polymorphism in fat regulation.
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spelling pubmed-26467032009-02-24 INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men Orkunoglu-Suer, Funda E Gordish-Dressman, Heather Clarkson, Priscilla M Thompson, Paul D Angelopoulos, Theodore J Gordon, Paul M Moyna, Niall M Pescatello, Linda S Visich, Paul S Zoeller, Robert F Harmon, Brennan Seip, Richard L Hoffman, Eric P Devaney, Joseph M BMC Med Genet Research Article BACKGROUND: A common SNP upstream of the INSIG2 gene, rs7566605 (g.-10,1025G>C, Chr2:118,552,255, NT_022135.15), was reported to be associated with obesity (Body Mass Index, [BMI]) in a genome-wide association scan using the Framingham Heart Study but has not been reproduced in other cohorts. As BMI is a relatively insensitive measure of adiposity that is subject to many confounding variables, we sought to determine the relationship between the INSIG2 SNP and subcutaneous fat volumes measured by MRI in a young adult population. METHODS: We genotyped the INSIG2 SNP rs7566605 in college-aged population enrolled in a controlled resistance-training program, (the Functional Polymorphism Associated with Human Muscle Size and Strength, FAMuSS cohort, n = 752 volunteers 18–40 yrs). In this longitudinal study, we examined the effect of the INSIG2 polymorphism on subcutaneous fat and muscle volumes of the upper arm measured by magnetic resonance imaging (MRI) before and after 12 wks of resistance training. Gene/phenotype associations were tested using an analysis of covariance model with age and weight as covariates. Further, the % variation in each phenotype attributable to genotype was determined using hierarchical models and tested with a likelihood ratio test. RESULTS: Women with a copy of the C allele had higher levels of baseline subcutaneous fat (GG: n = 139; 243473 ± 5713 mm(3 )vs. GC/CC: n = 181; 268521 ± 5003 mm(3); p = 0.0011); but men did not show any such association. Men homozygous for the G ancestral allele showed a loss of subcutaneous fat, while those with one or two copies of the C allele gained a greater percentage of subcutaneous fat with resistance training (GG: n = 103; 1.02% ± 1.74% vs. GC/CC: n = 93; 6.39% ± 1.82%; p = 0.035). CONCLUSION: Our results show that the INSIG2 rs7566605 polymorphism underlies variation in subcutaneous adiposity in young adult women and suppresses the positive effects of resistance training on men. This supports and extends the original finding that there is an association between measures of obesity and INSIG2 rs7566605 and further implicates this polymorphism in fat regulation. BioMed Central 2008-12-23 /pmc/articles/PMC2646703/ /pubmed/19105843 http://dx.doi.org/10.1186/1471-2350-9-117 Text en Copyright © 2008 Orkunoglu-Suer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Orkunoglu-Suer, Funda E
Gordish-Dressman, Heather
Clarkson, Priscilla M
Thompson, Paul D
Angelopoulos, Theodore J
Gordon, Paul M
Moyna, Niall M
Pescatello, Linda S
Visich, Paul S
Zoeller, Robert F
Harmon, Brennan
Seip, Richard L
Hoffman, Eric P
Devaney, Joseph M
INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title_full INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title_fullStr INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title_full_unstemmed INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title_short INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
title_sort insig2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646703/
https://www.ncbi.nlm.nih.gov/pubmed/19105843
http://dx.doi.org/10.1186/1471-2350-9-117
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