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中华临床实验室管理电子杂志 ›› 2023, Vol. 11 ›› Issue (03) : 163 -166,180. doi: 10.3877/cma.j.issn.2095-5820.2023.03.007

调查研究

山西地区心脑血管疾病患者CYP2C19基因多态性检测
任宇璐(), 王舒宁, 畅锴, 杨苗   
  1. 030032 山西太原,太原金域临床检验所有限公司
  • 收稿日期:2021-12-11 出版日期:2023-08-28
  • 通信作者: 任宇璐

Study of CYP2C19 gene polymorphism in patients with cardiovascular and cerebrovascular diseases in Shanxi Province

Yulu Ren(), Shuning Wang, Kai Chang, Miao Yang   

  1. Taiyuan KingMed Center for Clinical Laboratory, Taiyuan Shanxi 030032, China
  • Received:2021-12-11 Published:2023-08-28
  • Corresponding author: Yulu Ren
引用本文:

任宇璐, 王舒宁, 畅锴, 杨苗. 山西地区心脑血管疾病患者CYP2C19基因多态性检测[J]. 中华临床实验室管理电子杂志, 2023, 11(03): 163-166,180.

Yulu Ren, Shuning Wang, Kai Chang, Miao Yang. Study of CYP2C19 gene polymorphism in patients with cardiovascular and cerebrovascular diseases in Shanxi Province[J]. Chinese Journal of Clinical Laboratory Management(Electronic Edition), 2023, 11(03): 163-166,180.

目的

研究心脑血管疾病患者CYP2C19的基因多态性,分析其是否与年龄、性别差异有关,为氯吡格雷的个体化用药提供指导依据。

方法

使用荧光定量PCR法,测定送检的776例考虑接受氯吡格雷抗血栓治疗的心脑血管疾病患者的CYP2C19基因型,分析年龄、性别与其基因多态性的关系。

结果

共检测出4种基因型,分别为CYP2C19*1/*1(42.14%)、*2/*2(10.82%)、*3/*3(1.03%)、*3/*17(46.01%);3种代谢表型,分别为快代谢型即正常代谢型(42.14%)、中代谢型(46.01%)、慢代谢型(11.85%),代谢表型与相关报道中所占的频率相似;患者CYP2C19基因型和代谢表型与性别差异均有统计学意义(均P<0.05);患者CYP2C19基因型和代谢表型与年龄差异均无统计学意义(均P>0.05)。

结论

山西地区心脑血管疾病患者中以正常代谢型、中代谢型患者为主,符合亚洲人群分布,其中基因型为CYP2C19*1/*1与*3/*17的患者人数最多,同时尚不可认为可以根据CYP2C19基因型、代谢表型与年龄、性别的差异指导用药,还需根据患者自身情况给予个体化用药治疗。

Objective

Study the gene polymorphism of CYP2C19 in patients with cardiovascular and cerebrovascular diseases, analyze whether it is related to age and sex differences, and provide guidance for the individualized medication of clopidogrel.

Methods

Using real-time PCR, to monitor the genotype of CYP2C19 for 776 patients with cardiovascular and cerebrovascular diseases,who were considered to receive clopidogrel antithrombotic therapy,and the correlation between age, sex and their genetic polymorphisms was analyzed.

Results

Four genotypes were detected, which were CYP2C19*1/*1 (42.14%), *2/*2 (10.82%), *3/*3 (1.03%) and *3/*17 (46.01%). The three metabolic phenotypes were extensive metabolizer/EM (42.14%), intermediata metabolizer/IM (46.01%) and poor metabolizer/PM (11.85%). The metabolic phenotypes were similar to those of related report. The CYP2C19 genotype and metabolic phenotype was associated with an increased rate of male and female patients (all P<0.05). There was no significant difference among patients of different age in CYP2C19 genotype and metabolic phenotype (all P<0.05).

Conclusions

The patients with cardiovascular and cerebrovascular diseases in Shanxi are mainly EM and IM patients, which is in line with Asian population distribution, and the number of patients with genotype CYP2C19 *1/*1 and *3/*17 is the largest. At the same time, it can not be considered to be guided according to the differences of CYP2C19 genotype, metabolic phenotype and the age, sex in drug use, still need according to the patient's own situation to give individualized medication treatment.

表1 CYP2C19基因型和代谢表型检测结果(n=161)
表2 基因型与代谢表型的性别分布情况/例(%)
表3 基因型与代谢表型年龄分布情况/例(%)
1
HASAN M S, BASRI H B, HIN L P, et al. Genetic polymorphisms and drug interactions leading to clopidogrel resistance: Why the Asian population requires special attention[J]. The international journal of neuroscience, 2013, 123(3): 143-154.
2
杨瑞, 刘慧, 陈泽姮, 等. 临床药师基于CYP2C19基因检测指导氯吡格雷个体化用药及其疗效评价[J]. 中国临床药理学与治疗学, 2019, 24(8): 938-943.
3
董结芬. 药物基因检测指导氯吡格雷的临床用药价值研究[J]. 深圳中西医结合杂志, 2020, 30(15): 96-97.
4
CHEN D Y, WANG C Y, WEN M S, et al. Paraoxonase-1 is not a maor determinant of stent thrombosis in a Taiwanese population[J]. PLoS One, 2012, 7(6): e39178.
5
HULOT J S, BURA A, VILLARD E, et al. Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects[J]. Blood, 2006, 108(7): 2244-2247.
6
COLLET J P, HULO J S, PENA A, et al. Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: A cohort study[J]. Lancet (London, England), 2009, 373(9660): 309-317.
7
MEGA J L, CLOSE S L, WIVIOTT S D, et al. Cytochrome P-450 polymorphisms and response to clopidogrel[J]. New England journal of medicine, 2009, 360: 354-362.
8
SHULDINER A R, O'CONNELL J R, BLIDEN K P, et al. Association of cytochrome P450 2C19 genotype with the antiplateleteffect and clinical effcacy of clopidogrel therapy[J]. The journal of the American medical association, 2009, 302(8): 849-857.
9
FRÉRE C, CUISSET T, GABORIT B, et al. The CYP2C19*17 allele is associated with better platelet response to clopidogrel in patients admitted for non-ST acute coronary syndrome[J]. Journal of thrombosis and haemostasis, 2009, 7(8): 1409-1411.
10
SIBBING D, GEBHARD D, KOCH W, et al. Isolated and interactive impact of common CYP2C19 genetic variants on the antiplatelet effect of chronic clopidogrel therapy[J]. Journal of thrombosis and haemostasis, 2010, 8(8): 1685-1693.
11
TIROCH KA, SIBBING D, KOCH W, et al. Protective effect of the CYP2C19*17 polymorphismwith increased activation of clopidogrel on cardiovascular events[J]. American heart journal, 2010, 160(3): 506-512.
12
邵明凤. 内科急性心绞痛患者使用氯吡格雷治疗的临床效果研究[J]. 系统医学, 2022, 7(14): 103-106.
13
栾鹏娇. 氯吡格雷对冠心病介入治疗后发生心血管不良事件的预防效果观察[J]. 中国医药指南, 2022, 20(31): 95-97.
14
GOLUKHOVA E Z, RYABININA M N, BULAEVA N I, et al. Clopidogrel response variability: Impact of genetic polymorphism and platelet biomarkers for predicting adverse outcomes poststenting[J]. American journal of therapeutics, 2015, 22(3): 222-230.
15
付梦璐, 董若兰, 凃玲, 等. 氯吡格雷抵抗研究进展[J]. 医药导报, 2018, 37(2): 139-145.
16
FEFER P, MATETZKY S. The genetic basis of platelet responsiveness to clopidogrel. A critical review of the literature[J]. Thromb haemost, 2011, 106(2): 203-210.
17
MEGA J L, SIMON T, Collet J P, et al. Reduced-function CYP2C19 genotype and risk of adverse clinical outcomes among patients treated with clopidogrel predominantly for PCI: A meta-analysis[J]. The journal of the American medical association, 2010, 304(16): 1821-1830.
18
刘龙梅, 周双艳, 王仲朝, 等. 太原地区汉族冠心病患者CYP2C19基因多态性研究[J]. 实用检验医师杂志, 2018, 10(4): 216-219.
19
张红楠, 王强, 朱晓红, 等. CYP2C19基因指导冠心病患者经皮冠状动脉介人术后抗血小板药合理应用[J]. 药学实践杂志, 2018, 36(6): 518-521.
20
DEHBOZORGI M, KAMALIDEHGHAN B, HOSSEINI I, et al. Prevalence of the CYP2C19*2 (681 G>A), *3(636 G>A) and*17 (-806 C>T) alleles among an Iranian population of different ethnicities[J]. Molecular medicine reports, 2018, 17(3): 4195-4202.
21
郭秀彩, 银雪艳, 许启荣, 等. CYP2C19和ABCB1基因检测指导患者氯吡格雷个体化给药[J]. 今日药学, 2020, 30(1): 36-39.
22
WIVIOTT S D, BRAUNWALD E, MCCABE C H, et al. Prasugrel versus clopidogrel in patients with acute coronary syndromes[J]. The New England journal of medicine, 2007, 357(20): 2001-2015.
23
刘新正, 李晓龙. 血栓弹力图监测抗血小板药物抑制率在老年急性冠脉综合征患者临床治疗中的价值[J]. 临床血液学杂志, 2020, 33(6): 425-427.
24
司家章, 冯雪茹, 刘梅林. 老年患者服用不同剂量氯吡格雷、替格瑞洛的反应性及安全性分析[J]. 临床心血管病杂志, 2022, 38(6): 460-466.
25
梁晶星, 陈芳, 梁启明. 应用血栓弹力图比较替格瑞洛及氯吡格雷治疗急性冠脉综合征患者的临床疗效[J]. 基层医学论坛, 2022, 26(22): 22-24.
26
刘福波, 杨琨. 替格瑞洛在冠心病介入治疗中的应用及对患者凝血功能的影响[J]. 吉林医学, 2022, 43(6): 1599-1601.
27
钟诗龙, 韩雅玲, 陈纪言, 等. 氯吡格雷抗血小板治疗个体化用药基因型检测指南解读[J]. 中国实用内科杂志, 2015, 35(1): 38-41.
28
唐晓春, 刘猛, 丁俭, 等. 急性脑梗死患者氯吡格雷基因代谢类型与氯吡格雷抵抗的关系[J]. 江苏医药, 2020, 46(5): 483-486.
29
SCOTT S A, SANGKUHL K, STEIN C M, et al. Clinical pharmacogenetics implementation consortium guidelines for CYP2C19 genotype and clopidogrel therapy: 2013update[J]. Clinical pharmacology and therapeutics, 2013, 94(3): 317-323.
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