Key result
Pharmacogenetics plays a role in the administration of novel oral anticoagulants due to considerable interindividual variations, highlighting the need to identify clinically relevant SNPs.
This review highlights the potential future role of pharmacogenetics in optimizing the dosage of novel oral anticoagulants based on individual genetic variants.
Does not support routine pharmacogenetic NOAC dosing; leaves open SNP validation in prospective trials.
Novel oral anticoagulants (NOACs) are becoming a therapy of choice in everyday clinical practice after almost 50 years during which warfarin and related coumarin derivatives were used as the main anticoagulants. Advantages of NOACs over standard anticoagulants include their predictable pharmacodynamics and pharmacokinetics, stable plasma concentrations and less drug-drug and food-drug interactions. However, pharmacogenetics has its place in administration of NOACs, as considerable interindividual variations have been detected. In this review, previous findings in pharmacogenetics of dabigatran, rivaroxaban, apixaban and edoxaban are summarized, along with recommendations for studying genes encoding metabolically important enzymes for four selected NOACs. Future directions include identification of clinically relevant SNPs, and change in optimum dosage for patients who are carriers of significant variants.
No takes yet. Share an insight, caveat, or question.
Ašić et al. (2018) conducted a review in Anticoagulation therapy. Novel oral anticoagulants (NOACs) was evaluated. Pharmacogenetics plays a role in the administration of novel oral anticoagulants due to considerable interindividual variations, highlighting the need to identify clinically relevant SNPs.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: