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THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING

The GSTP1 c.313A>G polymorphism is a candidate to explain some of the individual differences in cardiorespiratory fitness phenotypes’ responses to aerobic exercise training. We aim to explore the association between the GSTP1 c.313A>G polymorphism and the response to low-high impact aerobic ex...

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Autores principales: Zarebska, A, Jastrzebski, Z, Kaczmarczyk, M, Ficek, K, Maciejewska-Karlowska, A, Sawczuk, M, Leońska-Duniec, A, Krol, P, Cieszczyk, P, Zmijewski, P, Eynon, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Institute of Sport in Warsaw 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203841/
https://www.ncbi.nlm.nih.gov/pubmed/25435667
http://dx.doi.org/10.5604/20831862.1120932
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author Zarebska, A
Jastrzebski, Z
Kaczmarczyk, M
Ficek, K
Maciejewska-Karlowska, A
Sawczuk, M
Leońska-Duniec, A
Krol, P
Cieszczyk, P
Zmijewski, P
Eynon, N
author_facet Zarebska, A
Jastrzebski, Z
Kaczmarczyk, M
Ficek, K
Maciejewska-Karlowska, A
Sawczuk, M
Leońska-Duniec, A
Krol, P
Cieszczyk, P
Zmijewski, P
Eynon, N
author_sort Zarebska, A
collection PubMed
description The GSTP1 c.313A>G polymorphism is a candidate to explain some of the individual differences in cardiorespiratory fitness phenotypes’ responses to aerobic exercise training. We aim to explore the association between the GSTP1 c.313A>G polymorphism and the response to low-high impact aerobic exercise training. Sixty-six Polish Caucasian women were genotyped for the GSTP1 c.313A>G polymorphism; 62 of them completed 12-week aerobic (50-75% HR(max)) exercise training and were measured for selected somatic features (body mass and BMI) and cardiorespiratory fitness indices – maximal oxygen uptake (VO(2max), maximum heart rate (HR(max)), maximum ventilation (V(Emax)) and anaerobic threshold (AT) – before and after the training period. Two-factor analysis of variance revealed a main training effect for body mass reduction (p=0.007) and BMI reduction (p=0.013), improvements of absolute and relative VO(2max) (both p<0.001), and increased V(Emax) (p=0.005), but not for changes in fat-free mass (FFM) (p=0.162). However, a significant training x GSTP1 c.313A>G interaction was found only for FFM (p=0.042), absolute and relative VO(2max) (p=0.029 and p=0.026), and V(Emax) (p=0.005). As the result of training, significantly greater improvements in VO(2max), V(Emax) and FFM were gained by the GG+GA group compared to the AA genotype group. The results support the hypothesis that heterogeneity in individual response to training stimuli is at least in part determined by genetics, and GSTP1 c.313A>G may be considered as one (of what appear to be many) target polymorphisms to influence these changes.
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spelling pubmed-42038412014-12-01 THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING Zarebska, A Jastrzebski, Z Kaczmarczyk, M Ficek, K Maciejewska-Karlowska, A Sawczuk, M Leońska-Duniec, A Krol, P Cieszczyk, P Zmijewski, P Eynon, N Biol Sport Original Article The GSTP1 c.313A>G polymorphism is a candidate to explain some of the individual differences in cardiorespiratory fitness phenotypes’ responses to aerobic exercise training. We aim to explore the association between the GSTP1 c.313A>G polymorphism and the response to low-high impact aerobic exercise training. Sixty-six Polish Caucasian women were genotyped for the GSTP1 c.313A>G polymorphism; 62 of them completed 12-week aerobic (50-75% HR(max)) exercise training and were measured for selected somatic features (body mass and BMI) and cardiorespiratory fitness indices – maximal oxygen uptake (VO(2max), maximum heart rate (HR(max)), maximum ventilation (V(Emax)) and anaerobic threshold (AT) – before and after the training period. Two-factor analysis of variance revealed a main training effect for body mass reduction (p=0.007) and BMI reduction (p=0.013), improvements of absolute and relative VO(2max) (both p<0.001), and increased V(Emax) (p=0.005), but not for changes in fat-free mass (FFM) (p=0.162). However, a significant training x GSTP1 c.313A>G interaction was found only for FFM (p=0.042), absolute and relative VO(2max) (p=0.029 and p=0.026), and V(Emax) (p=0.005). As the result of training, significantly greater improvements in VO(2max), V(Emax) and FFM were gained by the GG+GA group compared to the AA genotype group. The results support the hypothesis that heterogeneity in individual response to training stimuli is at least in part determined by genetics, and GSTP1 c.313A>G may be considered as one (of what appear to be many) target polymorphisms to influence these changes. Institute of Sport in Warsaw 2014-09-12 2014-12 /pmc/articles/PMC4203841/ /pubmed/25435667 http://dx.doi.org/10.5604/20831862.1120932 Text en Copyright © Biology of Sport 2014 http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zarebska, A
Jastrzebski, Z
Kaczmarczyk, M
Ficek, K
Maciejewska-Karlowska, A
Sawczuk, M
Leońska-Duniec, A
Krol, P
Cieszczyk, P
Zmijewski, P
Eynon, N
THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title_full THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title_fullStr THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title_full_unstemmed THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title_short THE GSTP1 c.313A>G POLYMORPHISM MODULATES THE CARDIORESPIRATORY RESPONSE TO AEROBIC TRAINING
title_sort gstp1 c.313a>g polymorphism modulates the cardiorespiratory response to aerobic training
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203841/
https://www.ncbi.nlm.nih.gov/pubmed/25435667
http://dx.doi.org/10.5604/20831862.1120932
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