scholarly journals DETERMINATION OF OPTIMAL CUT-OFF VALUE IN ON-CLOPIDOGREL PLATELET AGGREGATION BY VERIFYNOW P2Y12 SYSTEM BASED ON FUNCTIONAL CYP2C19 GENE VARIANTS

2011 ◽  
Vol 57 (14) ◽  
pp. E1146
Author(s):  
Takamichi Ono ◽  
Koichi Kaikita ◽  
Seiji Hokimoto ◽  
Koichiro Yamamoto ◽  
Yuji Miyazaki ◽  
...  
1981 ◽  
Author(s):  
M Yamamoto ◽  
K Watanabe ◽  
Y Ando ◽  
H Iri ◽  
N Fujiyama ◽  
...  

It has been suggested that heparin caused potentiation of aggregation induced by ADP or epinephrine. The exact mechanism of heparin-induced platelet activation, however, remained unknown. In this paper, we have investigated the role of anti-thrombin III ( AT ) in heparin-induced platelet activation using purified AT and AT depleted plasma. When ADP or epinephrine was added to citrated PRP one minute after addition of heparin ( 1 u/ml, porcine intestinal mucosal heparin, Sigma Co. USA ), marked enhancement of platelet aggregation was observed, compared with the degree of aggregation in the absence of heparin. However, in platelet suspensions prepared in modified Tyrode’s solution, heparin exhibited no potentiating effect on platelet aggregation induced by epinephrine or ADP. Potentiation of epinephrine- or ADP-induced platelet aggregation by heparin was demonstrated when purified AT was added to platelet suspensions at a concentration of 20 μg/ml. AT depleted plasma, which was prepared by immunosorption using matrix-bound antibodies to AT, retained no AT, while determination of α1-antitrypsinα2- macroglobulin and fibrinogen in AT depleted plasma produced values which corresponded to those of the original plasma when dilution factor was taken into account. The activities of coagulation factors were also comparable to those of the original plasma. Heparin exhibited potentiating effect on ADP- or epinephrine-induced aggregation of platelets in original plasma, but no effect in AT depleted plasma. When purified AT was added back to AT depleted plasma at a concentration of 20 μg/ml, potentiation of platelet aggregation by heparin was clearly demonstrated.Our results suggest that effect of heparin on platelet aggregation is also mediated by anti-thrombin III.


2020 ◽  
Vol 194 ◽  
pp. 95-97
Author(s):  
Makiko Yoshida ◽  
Kazumasa Oura ◽  
Mie Shimizu ◽  
Tatsunori Natori ◽  
Shinsuke Narumi ◽  
...  

2020 ◽  
Vol 21 (12) ◽  
pp. 889-897
Author(s):  
Moataz Ellithi ◽  
Jordan Baye ◽  
Russell A Wilke

Pharmacogenetic variants can alter the mechanism of action (pharmacodynamic gene variants) or kinetic processes such as absorption, distribution, metabolism and elimination (pharmacokinetic gene variants). Many initial successes in precision medicine occurred in the context of genes encoding the cytochromes P450 (CYP enzymes). CYP2C19 activates the antiplatelet drug clopidogrel, and polymorphisms in the CYP2C19 gene are known to alter the outcome for patients taking clopidogrel in the context of cardiovascular disease. CYP2C19 loss-of-function alleles are specifically associated with increased risk for coronary stent thrombosis and major adverse cardiovascular events in patients taking clopidogrel following percutaneous coronary intervention. We explore successes and challenges encountered as the clinical and scientific communities advance CYP2C19 genotyping in the context of routine patient care.


2016 ◽  
Vol 64 (S1) ◽  
pp. 99-107 ◽  
Author(s):  
Martin Petrek ◽  
Lenka Kocourkova ◽  
Veronika Zizkova ◽  
Zdenek Nosek ◽  
Milos Taborsky ◽  
...  

2019 ◽  
Vol 10 ◽  
Author(s):  
Simran Maggo ◽  
Martin A. Kennedy ◽  
Zoe A. Barczyk ◽  
Allison L. Miller ◽  
Julia J. Rucklidge ◽  
...  

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