Int J Sports Med 2013; 34(03): 274-280
DOI: 10.1055/s-0032-1316365
Genetics & Molecular Biology
© Georg Thieme Verlag KG Stuttgart · New York

GNAS A-1121G Variant is Associated with Improved Diastolic Dysfunction in Response to Exercise Training in Heart Failure Patients

A. J. Alves
1   Faculty of Sport, Research Centre in Physical Activity, Health and Leisure, University of Porto, Porto, Portugal
,
E. Goldhammer
2   Bnai-Zion Haifa Medical Center, Heart Institute, Haifa, Israel
,
F. Ribeiro
1   Faculty of Sport, Research Centre in Physical Activity, Health and Leisure, University of Porto, Porto, Portugal
6   CESPU, Polytechnic Health Institute of the North, Physiotherapy Department Gandra PRD
,
N. Eynon
3   Institute of Sports Exercise and Active Living, Victoria University, Melbourne, Australia
,
S. Ben-Zaken Cohen
4   Genetics and Molecular Biology Laboratory, The Zinman College of Physical Education and Sport Sciences at the Wingate Institute, Netanya, United States
,
J. A. Duarte
1   Faculty of Sport, Research Centre in Physical Activity, Health and Leisure, University of Porto, Porto, Portugal
,
J. L. Viana
5   School of Sport, Exercise and Health Sciences Loughborough, Loughborough University, United Kingdom
7   Research Center in Sports, Health Sciences and Human Development (CIDESD), Portugal
,
M. Sagiv
4   Genetics and Molecular Biology Laboratory, The Zinman College of Physical Education and Sport Sciences at the Wingate Institute, Netanya, United States
,
J. Oliveira
1   Faculty of Sport, Research Centre in Physical Activity, Health and Leisure, University of Porto, Porto, Portugal
› Author Affiliations
Further Information

Publication History



accepted after revision 22 May 2012

Publication Date:
12 October 2012 (online)

Abstract

β1-adrenergic receptors (ADRB1) and Gαs proteins (GNAS) play important roles in the regulation of cardiac function. The present study sought to investigate whether ADRB1 Arg389Gly (rs1801253), GNAS -1211 G/A (rs6123837) and GNAS 2291 C/T (rs6026584) variants are associated with left ventricular function and exercise tolerance in heart failure patients. 61 heart failure patients completed a 6-month exercise-training programme. Left ventricular ejection fraction (LVEF), mitral inflow velocities (deceleration time, and E/A ratio) and exercise tolerance (METs) were assessed at baseline and following exercise training. There were no associations between the studied variants and LVEF or E/A ratio measured at baseline and after exercise training. Deceleration time of early mitral flow was higher at baseline in GNAS -1211G allele carriers compared with -1211A allele homozygotes (P<0.05). Exercise training attenuated deceleration time in -1211G allele carriers (P<0.05) but not in -1211A allele homozygotes. Moreover, ADRB1 389Gly homozygotes had a greater training-induced increase in exercise tolerance than 389Arg homozygotes (P=0.04). This study shows that the functional GNAS -1121 G/A polymorphism is associated with diastolic function at baseline and in response to exercise training in heart failure patients. Furthermore, our data suggest that ADRB1 Arg389Gly polymorphism may influence exercise tolerance.

 
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