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本文引用的文献

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Lessons learned from the influence of CYP2C9 genotype on warfarin dosing.从CYP2C9基因分型对华法林剂量的影响中吸取的经验教训。
Expert Opin Drug Metab Toxicol. 2023 Apr;19(4):185-188. doi: 10.1080/17425255.2023.2220961. Epub 2023 Jun 2.
2
An Expiration Date for Pharmacogenetic Test Results and Prescribing Guidance?药物遗传学检测结果及处方指南的有效期?
J Appl Lab Med. 2023 Jul 5;8(4):826-830. doi: 10.1093/jalm/jfad016.
3
Using an electronic medical record patient portal for warfarin self-management: Empowering children and parents.使用电子病历患者门户进行华法林自我管理:赋予儿童和家长权力。
Res Pract Thromb Haemost. 2023 Feb 3;7(2):100066. doi: 10.1016/j.rpth.2023.100066. eCollection 2023 Feb.
4
Pharmacogenomics: current status and future perspectives.药物基因组学:现状与未来展望。
Nat Rev Genet. 2023 Jun;24(6):350-362. doi: 10.1038/s41576-022-00572-8. Epub 2023 Jan 27.
5
Genomewide Association Study Identifies Copy Number Variants Associated With Warfarin Dose Response and Risk of Venous Thromboembolism in African Americans.全基因组关联研究鉴定出与非裔美国人华法林剂量反应和静脉血栓栓塞风险相关的拷贝数变异。
Clin Pharmacol Ther. 2023 Mar;113(3):624-633. doi: 10.1002/cpt.2820. Epub 2023 Jan 19.
6
Optimizing warfarin dosing using deep reinforcement learning.使用深度强化学习优化华法林剂量。
J Biomed Inform. 2023 Jan;137:104267. doi: 10.1016/j.jbi.2022.104267. Epub 2022 Dec 7.
7
Evaluating the frequency and the impact of pharmacogenetic alleles in an ancestrally diverse Biobank population.评估一个具有多种族背景的生物库人群中药物遗传学等位基因的频率和影响。
J Transl Med. 2022 Nov 28;20(1):550. doi: 10.1186/s12967-022-03745-5.
8
Understanding the public health value and defining preferred product characteristics for therapeutic human papillomavirus (HPV) vaccines: World Health Organization consultations, October 2021-March 2022.理解治疗性人乳头瘤病毒(HPV)疫苗的公共卫生价值并确定其首选产品特征:世界卫生组织磋商,2021 年 10 月至 2022 年 3 月。
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9
The Impact of CYP2C9*11 Allelic Variant on the Pharmacokinetics of Phenytoin and (S)-Warfarin.CYP2C9*11 等位基因变异对苯妥英和(S)-华法林药代动力学的影响。
Clin Pharmacol Ther. 2022 Jul;112(1):156-163. doi: 10.1002/cpt.2613. Epub 2022 May 5.
10
Warfarin dosing strategies evolution and its progress in the era of precision medicine, a narrative review.华法林剂量策略的演变及其在精准医学时代的进展:叙述性综述。
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津巴布韦黑人队列的华法林药物遗传学:一项观察性前瞻性研究。

Warfarin pharmacogenetics in a black Zimbabwean cohort: an observational prospective study.

机构信息

Department of Genomic Medicine, African Institute of Biomedical Science & Technology, 911 Boronia Township, Beatrice, Zimbabwe.

Department of Biotechnology, Chinhoyi University of Technology, Private Bag 7724, Chinhoyi, Zimbabwe.

出版信息

Pharmacogenomics. 2023 Jul;24(10):529-538. doi: 10.2217/pgs-2023-0089. Epub 2023 Jul 12.

DOI:10.2217/pgs-2023-0089
PMID:37435666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10621760/
Abstract

A prospective observational study was conducted to evaluate the feasibility of implementing clinical guidelines for warfarin dosing in black Zimbabwean patients. , ,  and and  c. 1639 G>A variations were observed in 62 study patients. Overall, 39/62 (62.90%) participants did not receive a warfarin starting dose as would have been recommended by Clinical Pharmacogenetics Implementation Consortium guidelines. US FDA and Dutch Pharmacogenetics Working Group guidelines are based on and only, hence, unlikely useful in this cohort, where such variants were not detected. Clinical Pharmacogenetics Implementation Consortium guidelines, on the other hand, have a specific recommendation on the African-specific variants , and , and are hence suitable for implementation in Zimbabwe and would help optimize warfarin doses in patients in the study cohort.

摘要

一项前瞻性观察性研究评估了在津巴布韦黑人患者中实施华法林剂量临床指南的可行性。在 62 例研究患者中观察到 、 、 和 以及 1639 G>A 变异。总体而言,62 例患者中有 39 例(62.90%)未接受临床药物遗传学实施联盟指南推荐的华法林起始剂量。美国 FDA 和荷兰药物遗传学工作组指南仅基于 和 ,因此,在未检测到这些变异的情况下,不太可能对本队列有用。另一方面,临床药物遗传学实施联盟指南对华法林剂量有特定的推荐,适用于在津巴布韦实施,并有助于优化研究队列中患者的华法林剂量。