精确使用抗凝剂来减少药物不良反应:我们还在那里吗?
Benjamin Cross1, Richard M Turner1,2, J Eunice Zhang1
1Wolfson Centre for Personalised Medicine, Institute of Systems, Molecular and Integrative Biology, The University of Liverpool, 1-5 Brownlow Street, Liverpool, L69 3GL, UK.
The pharmacogenomics journal
|March 5, 2024
概括
了解抗凝剂的变性是提高患者安全的关键. 遗传和临床因素影响药物反应,需要个性化剂量和监测策略以获得更好的结果.
科学领域:
- 药物基因组学 药物基因组学
- 临床药理学 临床药理学
- 药品安全 药品安全
背景情况:
- 抗凝剂是医疗的关键药物,随着医疗保健成本的上升.
- 对抗凝血剂反应的个体间变化可能导致血栓形成或出血.
- 直接口服抗凝剂 (DOAC) 和肝素越来越多地与华法林一起被处方.
研究的目的:
- 审查影响抗凝剂反应变异性的因素.
- 探索针对患者子组量身定制抗凝剂治疗的证据.
- 确定对抗凝血剂安全性的未来研究领域.
主要方法:
- 对影响抗凝剂反应的遗传,环境和临床因素的文献综述.
- 对个性化剂量和监测策略的现有证据的分析.
- 识别知识缺口和未来的研究方向.
主要成果:
- 遗传变异 (VKORC1,CYP2C9,CYP4F2) 影响华法林反应,基因型知情剂量提高了安全性.
- CES1多态可能会影响达比加特兰暴露,但临床结果数据有限.
- 体重和抗Xa水平需要进一步调查低分子量肝素 (LMWH) 反应和临床结果.
结论:
- 根据遗传和临床因素来个性化抗凝剂治疗可以提高安全性.
- 需要进一步的研究,以优化高风险患者子组的治疗策略.
- 对于有效的抗凝药来说,更深入地了解反应变异性是必不可少的.
相关概念视频
Anticoagulant Drugs: Low-Molecular-Weight Heparins
696
Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
696
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
1.2K
Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.2K
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
523
Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
523
Therapeutic Index
4.3K
The therapeutic index of a drug is a key parameter in pharmacology that quantifies the relative safety of a drug by calculating the ratio between the dose that causes toxicity in half the population (50%) to the dose that proves to be effective for half the population (50%). It provides a spectrum of doses for a particular drug ranging from effective to potentially toxic. To illustrate, consider an anticoagulant agent like warfarin. It possesses a narrow window within its therapeutic index to...
4.3K
Clot Retraction and Fibrinolysis
5.9K
After a fibrin clot is formed, the next step is clot retraction, a vital process facilitated by platelet contractile proteins, such as actin and myosin. These proteins pull the fibrin strands closer together and condense the clot. This action reduces the size of the clot, creating a smaller, denser structure that effectively seals off the damaged vessel. Clot retraction consolidates the clot and helps with wound healing by bringing the edges of the damaged blood vessel closer together.
5.9K
Combined Effects of Drugs: Antagonism
8.5K
The combined effects of drugs can result in various interactions, of which an important type is antagonism. Antagonism is a mechanism where one drug inhibits or counteracts the effects of another drug. Antagonism can occur through various means, including receptor binding, allosteric modulation, functional interaction, chemical reactions, and pharmacokinetic processes.
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
The most common type is receptor antagonism, where one drug acts as an antagonist to block the effects of another drug by...
8.5K


