氯吡格雷治疗的土耳其患者CYP2C19多态性的患病率:初步结果,2017

Q4 Pharmacology, Toxicology and Pharmaceutics Current Pharmacogenomics and Personalized Medicine Pub Date : 2021-08-10 DOI:10.2174/1875692118666210810092755
Belgin Susleyici, C. Ciftci, S. Yurdakul, M. Çevik, C. Akdeniz, I. P. Canbolat, G. Deliorman, A. Karaalp
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引用次数: 0

摘要

氯吡格雷是最常用的抗血小板药物之一,用于降低动脉粥样硬化症状的风险。CYP2C19酶参与氯吡格雷代谢,CYP2C19基因的几种遗传变异可影响氯吡格雷的临床疗效。尽管相关社区对氯吡格雷治疗前CYP2C19药物遗传学检测缺乏完全接受的指南,但我们认为,在人群基础上,确定变异频率对于预测治疗开始前的效率和可能的氯吡格雷相关风险非常重要。我们的目的是确定影响氯吡格雷处方土耳其心脏病患者酶活性的基因多态性分布。54例氯吡格雷处方患者纳入研究。利用微阵列平台检测CYP2C19*2、*3、*4、*5、*6、*7、*8、*9、*10和*17多态性的存在。*4、*5、*6、*7、*8、*9、*10多态性未检出变异等位基因。*1/*1基因型频率为38.89%,*1/*2基因型频率为16.67%,*2/*17基因型频率为11.11%,*1/*3基因型频率1.85%,*2/*3基因型频率1.85%,*1/*17基因型频率27.78%,*17/*17基因型频率1.85%。根据基因型分析,1.85%的患者为不良,29.63%为中等;27.78%为快速代谢产物,1.85%为超快速代谢产物。虽然我们的研究人群患者数量并不多,但由于中、快速和超快速代谢患者的频率较高,CYP2C19多态性在土耳其心脏病患者中检测到的效率和可能的氯吡格雷相关风险应考虑在内。
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Prevalence of CYP2C19 Polymorphisms in Clopidogrel Treated Turkish Patients: Preliminary Results, 2017
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. 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. 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. 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.
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来源期刊
Current Pharmacogenomics and Personalized Medicine
Current Pharmacogenomics and Personalized Medicine Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
11
期刊介绍: Current Pharmacogenomics and Personalized Medicine (Formerly ‘Current Pharmacogenomics’) Current Pharmacogenomics and Personalized Medicine (CPPM) is an international peer reviewed biomedical journal that publishes expert reviews, and state of the art analyses on all aspects of pharmacogenomics and personalized medicine under a single cover. The CPPM addresses the complex transdisciplinary challenges and promises emerging from the fusion of knowledge domains in therapeutics and diagnostics (i.e., theragnostics). The journal bears in mind the increasingly globalized nature of health research and services.
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