dc.contributor.author |
Dogot, Marta |
|
dc.contributor.author |
Popa, Ana |
|
dc.date.accessioned |
2020-08-18T12:09:12Z |
|
dc.date.available |
2020-08-18T12:09:12Z |
|
dc.date.issued |
2018 |
|
dc.identifier.citation |
DOGOT, Marta, POPA, Ana. Therapy with clopidogrel based on CYP2C19 genotype. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 99-100. |
en_US |
dc.identifier.uri |
https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf |
|
dc.identifier.uri |
http://repository.usmf.md/handle/20.500.12710/11416 |
|
dc.description |
Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova |
en_US |
dc.description.abstract |
Introduction. Combined therapy, clopidogrel plus aspirin, prevents secondary thrombotic in
acute coronary syndromes (ACS), after percutaneous coronary interventions (PCI) with
placement of a coronary artery stent. Clopidogrel is activated in the liver by cytochrome P450
enzymes. CYP2C19 is the principal enzyme. The most common loss-of-function variant is CYP2C19*2. This contributes to the decrease in the active metabolite of clopidogrel in the blood
and reduce the effectiveness of clopidogrel therapy. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
MedEspera |
en_US |
dc.subject |
CYP2C19 genotype |
en_US |
dc.subject |
clopidogrel |
en_US |
dc.title |
Therapy with clopidogrel based on CYP2C19 genotype |
en_US |
dc.type |
Article |
en_US |