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The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men

BACKGROUND: The Gly482Ser polymorphism in peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PPARGC1A) has been demonstrated to be associated with diabetes, obesity and hypertension, all of which are important risk factors for left ventricular diastolic dysfunction. METHODS: The P...

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Autores principales: Ingelsson, Erik, Bennet, Louise, Ridderstråle, Martin, Söderström, Marianne, Råstam, Lennart, Lindblad, Ulf
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637232/
https://www.ncbi.nlm.nih.gov/pubmed/19077249
http://dx.doi.org/10.1186/1471-2261-8-37
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author Ingelsson, Erik
Bennet, Louise
Ridderstråle, Martin
Söderström, Marianne
Råstam, Lennart
Lindblad, Ulf
author_facet Ingelsson, Erik
Bennet, Louise
Ridderstråle, Martin
Söderström, Marianne
Råstam, Lennart
Lindblad, Ulf
author_sort Ingelsson, Erik
collection PubMed
description BACKGROUND: The Gly482Ser polymorphism in peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PPARGC1A) has been demonstrated to be associated with diabetes, obesity and hypertension, all of which are important risk factors for left ventricular diastolic dysfunction. METHODS: The PPARGC1A Gly482Ser polymorphism was genotyped in a community-based cohort of 499 men and 533 women, who also underwent an echocardiographic examination to determine their left ventricular diastolic function. The association between the polymorphism and the presence of diastolic dysfunction was evaluated using logistic regression models. RESULTS: The Ser allele of the PPARGC1A Gly482Ser polymorphism was significantly associated with a lower risk of diastolic dysfunction in men, but not in women. In a model adjusting for potential confounders (age, body mass index, leisure time physical activity, hypertension and diabetes) the results were still significant and substantial (odds ratio 0.13, 95% confidence interval 0.03–0.54, p for trend = 0.004). The results were consistent in a series of models, and they imply a multiplicative, protective effect of the Ser allele, with lower risk of diastolic dysfunction for each copy of the allele. CONCLUSION: The Ser allele of the PPARGC1A Gly482Ser polymorphism was associated with decreased risk of diastolic left ventricular dysfunction in men, but not in women, in our large community-based sample. It was associated with a substantially decreased risk, even after adjustment for potential confounders. The clinical importance of the findings has to be established in further studies.
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spelling pubmed-26372322009-02-07 The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men Ingelsson, Erik Bennet, Louise Ridderstråle, Martin Söderström, Marianne Råstam, Lennart Lindblad, Ulf BMC Cardiovasc Disord Research Article BACKGROUND: The Gly482Ser polymorphism in peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PPARGC1A) has been demonstrated to be associated with diabetes, obesity and hypertension, all of which are important risk factors for left ventricular diastolic dysfunction. METHODS: The PPARGC1A Gly482Ser polymorphism was genotyped in a community-based cohort of 499 men and 533 women, who also underwent an echocardiographic examination to determine their left ventricular diastolic function. The association between the polymorphism and the presence of diastolic dysfunction was evaluated using logistic regression models. RESULTS: The Ser allele of the PPARGC1A Gly482Ser polymorphism was significantly associated with a lower risk of diastolic dysfunction in men, but not in women. In a model adjusting for potential confounders (age, body mass index, leisure time physical activity, hypertension and diabetes) the results were still significant and substantial (odds ratio 0.13, 95% confidence interval 0.03–0.54, p for trend = 0.004). The results were consistent in a series of models, and they imply a multiplicative, protective effect of the Ser allele, with lower risk of diastolic dysfunction for each copy of the allele. CONCLUSION: The Ser allele of the PPARGC1A Gly482Ser polymorphism was associated with decreased risk of diastolic left ventricular dysfunction in men, but not in women, in our large community-based sample. It was associated with a substantially decreased risk, even after adjustment for potential confounders. The clinical importance of the findings has to be established in further studies. BioMed Central 2008-12-11 /pmc/articles/PMC2637232/ /pubmed/19077249 http://dx.doi.org/10.1186/1471-2261-8-37 Text en Copyright © 2008 Ingelsson 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
Ingelsson, Erik
Bennet, Louise
Ridderstråle, Martin
Söderström, Marianne
Råstam, Lennart
Lindblad, Ulf
The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title_full The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title_fullStr The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title_full_unstemmed The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title_short The PPARGC1A Gly482Ser polymorphism is associated with left ventricular diastolic dysfunction in men
title_sort ppargc1a gly482ser polymorphism is associated with left ventricular diastolic dysfunction in men
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637232/
https://www.ncbi.nlm.nih.gov/pubmed/19077249
http://dx.doi.org/10.1186/1471-2261-8-37
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