Τόμος 24 (2010) – Τεύχος 2 – Άρθρο 42 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 24 (2010) – Issue 2 – Article 42 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title Relationship between a polymorphism of the eNOS gene and myocardial infarction in a subgroup of Greek MI patients
Authors Chaido Dafni1, Dennis V. Cokkinos4, Olfert Landt2, Dimitris Panidis1, Martin Reczko3 and Nikolaos Drakoulis1

1. Department of Pharmaceutical Technology, School of Pharmacy, University of Athens, Panepistimiopolis Zografou, GR-15771, Athens, Hellas

2. TIB MOLBIOL, 22-23 Eresburstrasse, D-12103 Berlin, Germany

3. Institute of Molecular Oncology, Biomedical Sciences Research Center Alexander Fleming, P.O. Box 74145, GR-16602, Vari, Hellas

4. 1st Cardiology Department, Onassis Cardiac Surgery Center, 356 Sygrou Avenue, GR-17674 Kallithea, Athens, Hellas

Citation Dafni, C., Cokkinos, D.V., Landt, O., Panidis, D. et al.: Relationship between a polymorphism of the eNOS gene and myocardial infarction in a subgroup of Greek MI patients, Epitheorese Klin. Farmakol. Farmakokinet. 24(2): 130-132 (2010)
Publication Date 2010
Full Text Language English
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Keywords eNOS gene, myocardial infarction, nitric oxide synthase, nitric oxide.
Other Terms Review article
Summary Nitric oxide (NO), produced by endothelial nitric oxide synthase (eNOS), plays a key role in the regulation of vascular tone. The E298D polymorphic variant of eNOS has been associated with myocardial infarction (MI), but data relating to this variant are divergent in Greece. Accordingly, we examined a possible association between the E298D polymorphism of the eNOS gene and MI in a subgroup of the Greek population. The study population consisted of 204 patients with a history of MI and 218 control subjects. All subjects were of Greek origin. According to the univariate findings, the risk for MI in E298D TT was 2.06 (95%CI: 1.06-4.00, p=0.032) versus GG+GT and 2.34 (95%CI: 1.17-4.68, p=0.016) versus GG. The risk for the T allele was estimated at 1.42 (95%CI, 1.06-1.89, p=0.022) as compared to G allele. The positive association of TT versus GG+GT with MI risk remained even after adjusting for the main study covariates. Moreover, strong evidence was found for an increased risk for MI among carriers of the TT genotype who were smokers, hypertensive and had a family history of CAD. This study indicates that E298D polymorphism of the eNOS gene seems to be associated with MI occurrence in the Greek population. It is possible that TT genotype is closely linked to the etiology of MI even after adjusting for known MI risk factors.
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