Inherited Platelet Glycoprotein Polymorphisms and a Risk for Coronary Heart Disease in Young Central Europeans

• Published in: Thrombosis research Vol. 90; no. 3; pp. 117 - 123
• Main Authors: Sperr, Wolfgang R., Huber, Kurt, Roden, Michael, Janisiw, Michael, Lang, Thomas, Graf, Senta, Maurer, Gerd, Mayr, Wolfgang R., Panzer, Simon
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Ltd 01.05.1998; Elsevier Science
• Subjects: Adolescent - physiology; Adult; Aged; Aged, 80 and over; Alleles; Antigens, Human Platelet - genetics; Biological and medical sciences; Cardiology. Vascular system; Coronary artery disease; Coronary Disease - epidemiology; Coronary Disease - genetics; Coronary heart disease; Diabetes Mellitus - epidemiology; Diabetic Angiopathies - epidemiology; Europe - epidemiology; Female; Gene Frequency; Heart; Human platelet antigens; Humans; Male; Medical sciences; Middle Aged; Platelet glycoproteins; Platelet Membrane Glycoproteins - genetics; Polymorphism, Genetic - genetics; Polymorphisms; Risk Factors; Smoking - epidemiology; Central Europe; Europe; HPA, human platelet antigen; DM, diabetes mellitus; Platelet glycoproteins; Polymorphisms; Coronary artery disease; Human platelet antigens; CAD, coronary artery disease; Antigen; Human; Platelet; Young adult; Risk factor; Cardiovascular disease; Glycoproteins; Coronary heart disease; Polymorphism
• ISSN: 0049-3848; 1879-2472
• DOI: 10.1016/S0049-3848(98)00042-5

Among central Europeans polymorphisms of GPIIIa, GPIb, GPIIb, and GPIa named human platelet antigen-1 (HPA-1), -2, -3, and -5 are the clinically most relevant systems in which alloimmunization occurs. These genetically determined polymorphisms of glycoproteins may render platelets sensible for plaque formation and thus could increase risk for coronary artery disease (CAD). We therefore determined gene frequencies of HPA-1, -2, -3, and -5 in European patients suffering from CAD ( n=92; median age, 46 years) or CAD accompanied by diabetes mellitus (DM) ( n=30; median age, 60 years, DM I/II, 5/25) and compared the data obtained with those in DM patients without CAD ( n=80; median age, 43 years; DM I/II, 53/27) and a control group (newborns, n=906). Triglyceride and cholesterin levels as well as the percentage of smokers was significantly higher in the CAD group compared with the diabetics without DM ( p<0.005). No significant difference of the frequencies of any HPA-type between CAD patients with or without DM, diabetics, or controls could be detected. This was also true when evaluating a subgroup of patients aged 45 years or younger. To include a mutual influence of the described HPA-polymorphisms, we condensed the four HPA genotypes to joint glycoprotein variants. Again the same frequencies were found in patient groups and controls, when analyzing the five most common condensed joint glycoprotein variants. The analysis of the combined published studies shows that the pooled HPA-1 allele frequencies are identical in controls and CAD patients. Thus, no significant association between the polymorphisms of any of the studied HPA systems and the development of CAD can be found in central Europeans.