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One Rare Warfarin Resistance Case and Possible Mechanism Exploration

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 baseli...

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Autores principales: Zhao, Li, Zhai, Zhenguo, Li, Pengmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290475/
https://www.ncbi.nlm.nih.gov/pubmed/37359384
http://dx.doi.org/10.2147/PGPM.S404474
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author Zhao, Li
Zhai, Zhenguo
Li, Pengmei
author_facet Zhao, Li
Zhai, Zhenguo
Li, Pengmei
author_sort Zhao, Li
collection PubMed
description 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.
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spelling pubmed-102904752023-06-25 One Rare Warfarin Resistance Case and Possible Mechanism Exploration Zhao, Li Zhai, Zhenguo Li, Pengmei Pharmgenomics Pers Med Case Report 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. Dove 2023-06-20 /pmc/articles/PMC10290475/ /pubmed/37359384 http://dx.doi.org/10.2147/PGPM.S404474 Text en © 2023 Zhao et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Report
Zhao, Li
Zhai, Zhenguo
Li, Pengmei
One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title_full One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title_fullStr One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title_full_unstemmed One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title_short One Rare Warfarin Resistance Case and Possible Mechanism Exploration
title_sort one rare warfarin resistance case and possible mechanism exploration
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290475/
https://www.ncbi.nlm.nih.gov/pubmed/37359384
http://dx.doi.org/10.2147/PGPM.S404474
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