Key result
Genetic alterations in ~30 genes drive VKA dosing variability, supporting NOAC use in difficult cases.
Why the study?
VKA dosing varies widely due to environmental and genetic factors, prompting a review of genetic alterations affecting VKA sensitivity or resistance and the role of NOACs.
Genetic polymorphisms in CYP2C9 and VKORC significantly influence inter-individual variability in VKA dosing, highlighting the potential utility of NOACs in patients with genetic resistance or sensitivity.
May support NOAC preference in genetically variable VKA cases; leaves open need for prospective genotype-guided trials.
Anticoagulant treatment is extremely important and frequently encountered in the therapy of various cardiovascular diseases. Vitamin K antagonists (VKA) are in use for the prevention and treatment of arterial and venous thromboembolism, despite the introduction of new direct-acting oral anticoagulants (NOAC). The VKA still have the clear recommendation in patients with a mechanical prosthetic heart valve replacement or moderate to severe mitral stenosis of the rheumatic origin, in deep vein thrombosis associated with congenital thrombophilia, and in cases where NOAC are prohibited by social condition (financial reason) or by comorbidities (extreme weight, severe renal or liver disease). VKA dosing required to reach the targeted therapeutic range varies largely between patients (inter-individual variability). This inter-individual variability depends on multiple environmental factors such as age, mass, diet, etc. but it is also influenced by genetic determinism. About 30 genes implicated in the metabolism coumarins derivatives were identified, the most important being CYP2C9 and VKORC, each with several polymorphisms. Herein, we review the data regarding genetic alterations in general and specific populations, highlight the diagnosis options in particular cases presenting with genetic alteration causing higher sensitivity and/or resistance to VKA therapy and underline the utility of NOAC in solving such rare and difficult problems.
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Cîmpan et al. (2019) conducted a review in Cardiovascular diseases requiring anticoagulant therapy. Vitamin K antagonists (VKA) and NOACs was evaluated. Genetic alterations in about 30 genes, particularly CYP2C9 and VKORC, influence inter-individual variability in Vitamin K antagonist dosing, highlighting the utility of NOACs in difficult cases.
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