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Published in: BMC Medical Genetics 1/2008

Open Access 01-12-2008 | Research article

Association of the 894G>T polymorphism in the endothelial nitric oxide synthase gene with risk of acute myocardial infarction

Authors: George K Andrikopoulos, Dimitris K Grammatopoulos, Stylianos E Tzeis, Sevasti I Zervou, Dimitris J Richter, Michalis N Zairis, Elias J Gialafos, Dimitris C Sakellariou, Stefanos G Foussas, Antonis S Manolis, Christodoulos I Stefanadis, Pavlos K Toutouzas, Edward W Hillhouse, The GEMIG study investigators

Published in: BMC Medical Genetics | Issue 1/2008

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Abstract

Background

This study was designed to investigate the association of the 894G>T polymorphism in the eNOS gene with risk of acute myocardial infarction (AMI), extent of coronary artery disease (CAD) on coronary angiography, and in-hospital mortality after AMI.

Methods

We studied 1602 consecutive patients who were enrolled in the GEMIG study. The control group was comprised by 727 individuals, who were randomly selected from the general adult population.

Results

The prevalence of the Asp298 variant of eNOS was not found to be significantly and independently associated with risk of AMI (RR = 1.08, 95%CI = 0.77–1.51, P = 0.663), extent of CAD on angiography (OR = 1.18, 95%CI = 0.63–2.23, P = 0.605) and in-hospital mortality (RR = 1.08, 95%CI = 0.29–4.04, P = 0.908).

Conclusion

In contrast to previous reports, homozygosity for the Asp298 variant of the 894G>T polymorphism in the eNOS gene was not found to be associated with risk of AMI, extent of CAD and in-hospital mortality after AMI
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Metadata
Title
Association of the 894G>T polymorphism in the endothelial nitric oxide synthase gene with risk of acute myocardial infarction
Authors
George K Andrikopoulos
Dimitris K Grammatopoulos
Stylianos E Tzeis
Sevasti I Zervou
Dimitris J Richter
Michalis N Zairis
Elias J Gialafos
Dimitris C Sakellariou
Stefanos G Foussas
Antonis S Manolis
Christodoulos I Stefanadis
Pavlos K Toutouzas
Edward W Hillhouse
The GEMIG study investigators
Publication date
01-12-2008
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2008
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-9-43

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