Why the study?
Does the human platelet antigen-1 (HPA-1) polymorphism influence the antiplatelet effects of glycoprotein IIb/IIIa inhibitors?
Does the human platelet antigen-1 (HPA-1) polymorphism influence the antiplatelet effects of glycoprotein IIb/IIIa inhibitors?
The HPA-1 polymorphism does not explain the inter-individual variability in the antiplatelet effects of clinically used GPIIb/IIIa inhibitors.
Animal data indicate no HPA-1 effect on GPIIb/IIIa inhibition; leaves open relevance to human pharmacogenetics.
This study investigated the hypothesis that the human platelet antigen-1 (HPA-1) polymorphism may influence the antiplatelet effects of glycoprotein (GP)IIb/IIIa inhibitors. Adenosine diphosphate (30 micro mol)-induced fibrinogen binding was measured by flow cytometry. Abciximab (0.03-3 micro g/ml), tirofiban (0.3-30 nmol/l) or eptifibatide (0.01-1 micro g/ml) were incubated for 15 min with the samples prior to stimulation. IC(50) values for the inhibition of fibrinogen binding were determined from each experiment. All subjects were genotyped by GALIOS and automated fluorescence correlation spectroscopy. Although a marked variability in the inhibitory effects of all three GPIIb/IIIa inhibitors was confirmed, there were no significant differences between the genotypes with respect to the inhibition of fibrinogen binding. Thus, the present study does not provide evidence for an effect of HPA-1 polymorphism on the inter-individual variability in the platelet inhibitory effects of the three GPIIb/IIIa inhibitors approved for clinical use.
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Weber et al. (2002) studied this question.
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