Abstract
The renin–angiotensin system (RAS) plays an important role in regulating the main characteristics of cardiovascular functions. The aim of the study is to test possible associations of ACE I/D polymorphism with coronary artery disease (CAD) and diabetes evaluated together in 600 persons with coronarography. Four groups of patients (the CAD + DM + patients with both CAD and diabetes, the CAD + DM − patients with CAD, the CAD − DM + with only diabetes, and the CAD − DM − without CAD as well as diabetes) were compared in ACE I/D polymorphism, intermediate phenotypes (hemodynamic and metabolic parameters), and pharmacological therapy. We proved a number of significant differences especially between the CAD + DM + and CAD − DM − groups. Although the patients had been treated according to their clinical state, we were able to prove significant differences between ACE I/D genotypes (in the model of heterozygote advantage) in these groups (hypertension, obesity, BMI, renal insufficiency, more cardiovascular risk factors, some inflammatory factors, glycemia, and lipid profile). The drugs were administrated more frequently to the DD + II carriers, which further supports the heterozygote advantage hypothesis tested in the study. We proved a heterozygote advantage model for ACE I/D polymorphism, CAD, and diabetes mellitus confirmed by associations with intermediate phenotypes and by therapy schedule.
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Acknowledgments
The study was supported by the project IGA NS10206-3/2009 of the Ministry of Health of the Czech Republic.
Special thanks to Prof. Jaroslav Meluzín, MD, CSc. and Vladimír Kincl, MD from the 1st Department of Internal Medicine/Cardioangiology, St. Ann’s Faculty Hospital Brno, Faculty of Medicine, Masaryk University for providing clinical data databases.
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Vasku, A., Blahak, J., Baumgartner, D., Bienertova-Vasku, J. (2011). Angiotensin Converting Enzyme I/D Polymorphism and Cardiovascular Risk: Disclosed Story. In: Ostadal, B., Nagano, M., Dhalla, N. (eds) Genes and Cardiovascular Function. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-7207-1_13
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DOI: https://doi.org/10.1007/978-1-4419-7207-1_13
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