“…These include CYP2C19 singlenucleotide polymorphisms, age, body mass index, diabetes mellitus, renal function, C-reactive protein, fibrinogen, and endothelial function. 18,[21][22][23][24][25][26] In this study, we simultaneously measured peripheral endothelial function by RHI and evaluated RPR in a population lacking CYP2C19*2 or *3 loss-offunction allele, selected specifically to avoid the effects of this gene on platelet activity. The results identified peripheral endothelial dysfunction as a significant determinant of high RPR in patients with stable CAD.…”