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一例罕见的华法林抵抗病例及可能机制探讨

One Rare Warfarin Resistance Case and Possible Mechanism Exploration.

作者信息

Zhao Li, Zhai Zhenguo, Li Pengmei

机构信息

Pharmacy Department, China-Japan Friendship Hospital, Beijing, People's Republic of China.

Department of Respiratory and Critical Care Medicine, China-Japan Friendship Hospital, Beijing, People's Republic of China.

出版信息

Pharmgenomics Pers Med. 2023 Jun 20;16:609-615. doi: 10.2147/PGPM.S404474. eCollection 2023.

DOI:10.2147/PGPM.S404474
PMID:37359384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10290475/
Abstract

One 59-year-old female patient with deep venous thrombosis (DVT) and pulmonary embolism (PE) was treated with 6 mg warfarin once daily as an anticoagulant. Before taking warfarin, her international normalized ratio (INR) was 0.98. Two days after warfarin treatment, her INR did not change from baseline. Due to the high severity of the PE, the patient needed to reach her target range (INR goal = 2.5, range = 2~3) rapidly, so the dose of warfarin was increased from 6 mg daily to 27 mg daily. However, the patient's INR did not improve with the dose escalation, still maintaining an INR of 0.97-0.98. We drew a blood sample half an hour before administering 27 mg warfarin and detected single nucleotide polymorphism for the following genes, which were identified to be relevant with warfarin resistance: CYP2C9 rs1799853, rs1057910, VKORC1 rs9923231, rs61742245, rs7200749, rs55894764, CYP4F2 rs2108622, and GGCX rs2592551. The trough plasma concentration of warfarin was 196.2 ng/mL after 2 days of warfarin administration with 27 mg QD, which was much lower than the therapeutic drug concentration ranges of warfarin (500-3,000 ng/mL). The genotype results demonstrate that the CYP4F2gene has rs2108622 mutation which can explain some aspect of warfarin resistance. Further investigations are necessary to fully characterize other pharmacogenomics or pharmacodynamics determinants of warfarin dose-response in Chinese.

摘要

一名59岁患有深静脉血栓形成(DVT)和肺栓塞(PE)的女性患者,接受每日一次6毫克华法林作为抗凝治疗。服用华法林前,她的国际标准化比值(INR)为0.98。华法林治疗两天后,她的INR与基线相比没有变化。由于PE的严重程度较高,患者需要迅速达到目标范围(INR目标值 = 2.5,范围 = 2~3),因此将华法林剂量从每日6毫克增加到每日27毫克。然而,随着剂量增加,患者的INR并未改善,仍维持在0.97 - 0.98。在给予27毫克华法林前半小时采集血样,检测了以下与华法林抵抗相关基因的单核苷酸多态性:CYP2C9 rs1799853、rs1057910、VKORC1 rs9923231、rs61742245、rs7200749、rs55894764、CYP4F2 rs2108622和GGCX rs2592551。给予27毫克/日华法林治疗2天后,华法林的谷血浆浓度为196.2纳克/毫升,远低于华法林的治疗药物浓度范围(500 - 3000纳克/毫升)。基因型结果表明,CYP4F2基因存在rs2108622突变,这可以解释华法林抵抗的某些方面。有必要进一步研究以全面了解中国人华法林剂量反应的其他药物基因组学或药效学决定因素。

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Blood. 2018 Sep 27;132(13):1365-1371. doi: 10.1182/blood-2018-04-848333. Epub 2018 Jul 12.
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