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基因多态性对HVR患者华法林起始抗凝效果的影响
引用本文:丁征,邱罕凡,张振龙,张树亮,林美钦,张晶,宋洪涛. 基因多态性对HVR患者华法林起始抗凝效果的影响[J]. 药物流行病学杂志, 2014, 0(2): 98-101
作者姓名:丁征  邱罕凡  张振龙  张树亮  林美钦  张晶  宋洪涛
作者单位:南京军区福州总医院药学科(福州 350025);中国医学科学院阜外心血管病医院药剂科。;福建医科大学附属协和医院;;福建医科大学附属协和医院;;福建医科大学附属协和医院;;南京军区福州总医院药学科(福州 350025);;南京军区福州总医院药学科(福州 350025);;南京军区福州总医院药学科(福州 350025);
摘    要:目的:观察心脏瓣膜置换术后患者基线信息和CYP2C9*3、VKORC1-1639A/G基因多态性与术后华法林初始抗凝效果的关系。方法:收集患者的遗传信息和人口统计学信息,同时记录测得的INR值、华法林剂量、达标天数等。结果:纳入的172例患者中,VKORC1-1639AG型患者达到目标INR的时间与AA型相比约延长79.6%;CYP2C9*1/*3型患者达到目标INR的时间与*1/*1型相比约缩短50.9%;大部分VKORC1-1639AA(77.6%)和CYP2C9*1/*1(68.2%)基因型患者能够在术后第7日达到目标INR值;VKORC1-1639AG突变杂合子患者只有23%术后第7日达到目标INR值,且无抗凝过度现象;CYP2C9*1/*3突变杂合子患者全部达到目标INR值,且较易引起抗凝过度。结论:华法林起始抗凝阶段,VKORC1-1639AG突变型患者更难达到目标INR值,CYP2C9*1/*3突变型患者更易达到目标INR值。患者用药前可进行基因型检测,预测华法林用药剂量。

关 键 词:华法林  基因多态性  起始抗凝

Research on the Influence of VKORC1 and CYP2C9 Polymorphisms with Warfarin Initial Anticoagulant Effect
Ding Zheng,Qiu Hanfan,Zhang Zhenlong,Zhang Shuliang,Lin Meiqin,Zhang Jing and Song Hongtao. Research on the Influence of VKORC1 and CYP2C9 Polymorphisms with Warfarin Initial Anticoagulant Effect[J]. Chinese Journal of Pharmacoepidemiology, 2014, 0(2): 98-101
Authors:Ding Zheng  Qiu Hanfan  Zhang Zhenlong  Zhang Shuliang  Lin Meiqin  Zhang Jing  Song Hongtao
Affiliation:Ding Zheng Qiu Hanfan Zhang Zhenlong Zhang Shuliang Lin Meiqin Zhang Jing Song Hongtao Department of Pharmacy, Fuzhou General Hospital of Nanjing Military Command,Fuzhou 350025,China; 2. Union Hospital, Fujian Medical University ;3. Fuwai Cardiovacular Disease Hospital, Chinese Academy of Medical Sciences
Abstract:Objective:To explore the relationship between the baseline information and the reponse of VKORC1 and CYP2C9 polymorphisms of patients after heart valve replacement (HVR) to warfarin during initial anticoagulation. Methods:The patients' genetic and demographic information was collected and their INR value, dosage of warfarin and days of obtaining target INR value were recorded. Results : Of 172 consecutive patients, the mean time to target INR value for the patients with VKORCl-1639AG genotype were 79.6% longer than those with VKORCl-1639AA genotype; the mean time to target INR value for the patients with CYP2C9 * 1/* 3 genotype was 50.9% shorter than those with CYP2C9 * 1/ * 1 genotype; most patients with VKORCl-1639AA genotype or CYP2C9 * 1/* 1 genotype could reach the target INR val-ue on the seventh day postoperatively. Conclusion: It took longer time for the patients with VKORCl-1639AG genotype to obtain the target INR value and shorter time for patients with CYP2C9 * 1/* 3 genotype to obtain the target INR value. Pa-tients should have their genotype detection before taking the medicine to predict the dose of warfarin.
Keywords:Warfarin   Gene polymorphisms   Initial anticoagulation
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