Fol. Biol. 2009, 55, 187-191

https://doi.org/10.14712/fb2009055050187

Association of the eNOS 4a/b and -786T/C Polymormphisms with Coronary Artery Disease, Obesity and Diabetes Mellitus

Vladimír Kincl1, A. Vašků2, J. Meluzín1, R. Panovský1, J. Seménka1, L. Groch1

11st Department of Internal Medicine and Cardioangiology, St. Anne’s University Hospital, Faculty of Medicine, Masaryk University, Brno, Czech Republic
2Department of Pathophysiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic

Received January 2009
Accepted June 2009

The aim was to assess the relationship between eNOS 4a/b and -786T/C polymorphisms with coronary artery disease (CAD), obesity and diabetes mellitus. Total number of 1313 patients underwent coronary angiography, 939 had significant CAD (stenosis of ≥ 1 coronary artery ≥ 50%), 222 had smooth coronary arteries. Patients with insignificant atherosclerosis were excluded, the study finally comprised 1161 patients. The analysis of eNOS 4a/b and -786T/ C polymorphisms was performed by polymerase chain reaction. No significant interaction was found between -786T/C polymorphism and solitary CAD or CAD with diabetes and obesity. For 4a/b polymorphism, genotypes aa+ab were almost three times more frequent in diabetic patients without CAD versus patients without CAD and without diabetes – OR 2.79; P = 0.009, Pcorr = 0.03. In 4a/b polymorphism and CAD with obesity and diabetes: bb genotype was significantly more frequent: in patients with CAD, diabetes and obesity in comparison with obese diabetic patients without CAD (OR = 3.63, Pcorr = 0.05); in non-diabetic non-obese patients with CAD, versus diabetic and obese patients without CAD (OR = 3.38, Pcorr = 0.05); in obese non-diabetic patients without CAD vs. obese diabetic patients without CAD (OR = 5.91, Pcorr = 0.01); in patients without CAD, obesity and diabetes vs. obese diabetic patients without CAD (OR = 3.59, Pcorr = 0.05). The eNOS 4a/b polymorphism has significant association with diabetes mellitus in CAD-negative patients, and with CAD in combination with obesity and diabetes mellitus. No association between 4a/b or -786T/C polymorphism and solitary CAD was found.

Funding

This study was supported in part by grant of the Ministry of Education of the Czech Republic No. MSM 0021622402.

References

25 live references