Prevalence of CYP2C19 Polymorphisms in Clopidogrel Treated Turkish
Patients: Preliminary Results, 2017
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Published:2021-08
Issue:2
Volume:18
Page:116-122
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ISSN:1875-6921
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Container-title:Current Pharmacogenomics and Personalized Medicine
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language:en
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Short-container-title:CPPM
Author:
Susleyici Belgin1, Ciftci Cavlan2, Yurdakul Selen3, Cevik Mehtap1, Akdeniz Cansu Selcan3, Canbolat Ismail Polat3, Deliorman Gokce4, Karaalp Atila5
Affiliation:
1. Department of Molecular Biology, Marmara University Faculty of Science and Letters, Istanbul, Turkey 2. Department
of Cardiology, Demiroglu Bilim University Faculty of Medicine, Istanbul, Turkey 3. Department of Cardiology, Demiroglu Bilim University Faculty of Medicine, Istanbul, Turkey 4. Department of Software Engineering,
Faculty of Engineering and Architecture, Beykoz University, Istanbul, Turkey 5. Department of Medical Pharmacology,
Marmara University School of Medicine, Istanbul, Turkey
Abstract
Background:
Clopidogrel is one of the most frequently prescribed antiplatelet agents to reduce
the risk of atherosclerotic symptoms. CYP2C19 enzyme is involved in clopidogrel metabolism,
and several genetic variations of CYP2C19gene are able to affect the clinical response of clopidogrel.
Despite the lack of a fully accepted guideline for CYP2C19 pharmacogenetic testing before
clopidogrel treatment by relevant communities, we believe that determination of the variant frequencies
is important to predict the efficiency and possible clopidogrel related risks before the initiation of
treatment on the basis of populations. Our aim was to determine the distribution of gene polymorphisms
affecting the enzyme activity in Turkish cardiac patients prescribed clopidogrel.
Methods:
54 clopidogrel prescribed patients were included in the study. The presence of CYP2C19*2,
*3, *4, *5, *6, *7, *8, *9, *10 and *17 polymorphisms were investigated using a microarray platform.
Results :
No variant allele was detected for *4, *5, *6, *7, *8, *9 and *10 polymorphisms. The genotype
frequencies were detected as 38.89% for *1/*1, 16.67% for *1/*2, 11.11% for *2/*17, 1.85% for
*1/*3, 1.85% for *2/*3, 27.78% for *1/*17 and 1.85% for *17/*17. According to genotype analysis,
1.85% of the patients were recorded as poor and 29.63% intermediate; whereas 27.78% as rapid and
1.85% ultra-rapid metabolizers.
Conclusion:
Although our study population does not consist of a high number of patients, since the
high frequency of intermediate, rapid and ultra-rapid metabolizer patients were detected in relatively
high frequencies, CYP2C19 polymorphisms should be taken into account for efficiency and possible
clopidogrel related risks in Turkish cardiac patients.
Funder
Istanbul Development Agency
Publisher
Bentham Science Publishers Ltd.
Subject
Genetics (clinical),Pharmacology,Genetics,Molecular Biology,Molecular Medicine
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