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Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training
Glucocorticoid receptor (NR3C1) polymorphisms associate with obesity, muscle strength, and cortisol sensitivity. We examined associations among four NR3C1 polymorphisms and the muscle response to resistance training (RT). European-American adults (n = 602, 23.8±0.4yr) completed a 12 week unilateral...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731199/ https://www.ncbi.nlm.nih.gov/pubmed/26821164 http://dx.doi.org/10.1371/journal.pone.0148112 |
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author | Ash, Garrett I. Kostek, Matthew A. Lee, Harold Angelopoulos, Theodore J. Clarkson, Priscilla M. Gordon, Paul M. Moyna, Niall M. Visich, Paul S. Zoeller, Robert F. Price, Thomas B. Devaney, Joseph M. Gordish-Dressman, Heather Thompson, Paul D. Hoffman, Eric P. Pescatello, Linda S. |
author_facet | Ash, Garrett I. Kostek, Matthew A. Lee, Harold Angelopoulos, Theodore J. Clarkson, Priscilla M. Gordon, Paul M. Moyna, Niall M. Visich, Paul S. Zoeller, Robert F. Price, Thomas B. Devaney, Joseph M. Gordish-Dressman, Heather Thompson, Paul D. Hoffman, Eric P. Pescatello, Linda S. |
author_sort | Ash, Garrett I. |
collection | PubMed |
description | Glucocorticoid receptor (NR3C1) polymorphisms associate with obesity, muscle strength, and cortisol sensitivity. We examined associations among four NR3C1 polymorphisms and the muscle response to resistance training (RT). European-American adults (n = 602, 23.8±0.4yr) completed a 12 week unilateral arm RT program. Maximum voluntary contraction (MVC) assessed isometric strength (kg) and MRI assessed biceps size (cm(2)) pre- and post-resistance training. Subjects were genotyped for NR3C1 -2722G>A, -1887G>A, -1017T>C, and +363A>G. Men carrying the -2722G allele gained less relative MVC (17.3±1.2vs33.5±6.1%) (p = 0.010) than AA homozygotes; men with -1887GG gained greater relative MVC than A allele carriers (19.6±1.4vs13.2±2.3%) (p = 0.016). Women carrying the -1017T allele gained greater relative size (18.7±0.5vs16.1±0.9%) (p = 0.016) than CC homozygotes. We found sex-specific NR3C1 associations with the muscle strength and size response to RT. Future studies should investigate whether these associations are partially explained by cortisol’s actions in muscle tissue as they interact with sex differences in cortisol production. |
format | Online Article Text |
id | pubmed-4731199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47311992016-02-04 Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training Ash, Garrett I. Kostek, Matthew A. Lee, Harold Angelopoulos, Theodore J. Clarkson, Priscilla M. Gordon, Paul M. Moyna, Niall M. Visich, Paul S. Zoeller, Robert F. Price, Thomas B. Devaney, Joseph M. Gordish-Dressman, Heather Thompson, Paul D. Hoffman, Eric P. Pescatello, Linda S. PLoS One Research Article Glucocorticoid receptor (NR3C1) polymorphisms associate with obesity, muscle strength, and cortisol sensitivity. We examined associations among four NR3C1 polymorphisms and the muscle response to resistance training (RT). European-American adults (n = 602, 23.8±0.4yr) completed a 12 week unilateral arm RT program. Maximum voluntary contraction (MVC) assessed isometric strength (kg) and MRI assessed biceps size (cm(2)) pre- and post-resistance training. Subjects were genotyped for NR3C1 -2722G>A, -1887G>A, -1017T>C, and +363A>G. Men carrying the -2722G allele gained less relative MVC (17.3±1.2vs33.5±6.1%) (p = 0.010) than AA homozygotes; men with -1887GG gained greater relative MVC than A allele carriers (19.6±1.4vs13.2±2.3%) (p = 0.016). Women carrying the -1017T allele gained greater relative size (18.7±0.5vs16.1±0.9%) (p = 0.016) than CC homozygotes. We found sex-specific NR3C1 associations with the muscle strength and size response to RT. Future studies should investigate whether these associations are partially explained by cortisol’s actions in muscle tissue as they interact with sex differences in cortisol production. Public Library of Science 2016-01-28 /pmc/articles/PMC4731199/ /pubmed/26821164 http://dx.doi.org/10.1371/journal.pone.0148112 Text en © 2016 Ash 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 Ash, Garrett I. Kostek, Matthew A. Lee, Harold Angelopoulos, Theodore J. Clarkson, Priscilla M. Gordon, Paul M. Moyna, Niall M. Visich, Paul S. Zoeller, Robert F. Price, Thomas B. Devaney, Joseph M. Gordish-Dressman, Heather Thompson, Paul D. Hoffman, Eric P. Pescatello, Linda S. Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title | Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title_full | Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title_fullStr | Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title_full_unstemmed | Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title_short | Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training |
title_sort | glucocorticoid receptor (nr3c1) variants associate with the muscle strength and size response to resistance training |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731199/ https://www.ncbi.nlm.nih.gov/pubmed/26821164 http://dx.doi.org/10.1371/journal.pone.0148112 |
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