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Gewählte Publikation:

Zotz, RB; Winkelmann, BR; Nauck, M; Giers, G; Maruhn-Debowski, B; März, W; Scharf, RE.
Polymorphism of platelet membrane glycoprotein IIIa: human platelet antigen 1b (HPA-1b/PlA2) is an inherited risk factor for premature myocardial infarction in coronary artery disease.
Thromb Haemost. 1998; 79(4):731-735 Doi: 10.1055/s-0037-1615054
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Co-Autor*innen der Med Uni Graz
März Winfried
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Abstract:
Conflicting results of an association between the human platelet antigen 1b (HPA-1b or PlA2) allele and the risk of myocardial infarction and coronary artery disease have been reported. To assess the reason for this discrepancy, we determined the HPA-1 genotype in 298 men who had undergone coronary angiography, including 124 individuals with myocardial infarction, 83 individuals with coronary artery disease but no history of myocardial infarction, and 91 control patients. Among patients with acute or recent onset myocardial infarction (< 1 year), the prevalence of HPA-1b was higher than among patients with coronary artery disease but without myocardial infarction (33 percent vs. 14 percent, p = 0.016). In patients under 60 years of age this difference was even more pronounced (45 percent vs. 15 percent, p = 0.003). Unlike conventional risk factors HPA-1b does not represent a risk factor for coronary artery disease itself but appears to be associated with increased platelet thrombogenicity.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Age of Onset -
Antigens, Human Platelet - genetics
Coronary Disease - complications
Coronary Thrombosis - epidemiology
Disease Susceptibility - epidemiology
Female - epidemiology
Genotype - epidemiology
Humans - epidemiology
Male - epidemiology
Middle Aged - epidemiology
Myocardial Infarction - epidemiology
Platelet Glycoprotein GPIIb-IIIa Complex - genetics
Polymorphism, Genetic - genetics
Prospective Studies - genetics
Risk Factors - genetics
Survival Analysis - genetics
Thrombophilia - epidemiology

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