On the basis of the analysis of published data the role of P-glycoprotein, carrier protein, in rational pharmacotherapy in cardiology was shown on the example of its substrates-digoxin, antiplatelet agents and anticoagulants. Determination of C3435T polymorphism of multidrug resistance gene (MDR1), encoding P-glycoprotein, in pharmacotherapy with digoxin, antiplatelet drugs (clopidogrel tikagrelol, prasugrel) and anticoagulants (dabigatran etexilate, rivaroxaban, edoxaban) is not feasible in routine practice. Drug interactions have clinical implications for the efficacy and safety of pharmacotherapy in coadministration of these drugs with P-glycoprotein substrates, inducers and inhibitors.
CITATION STYLE
Shulkin, A. V., Yakusheva, E. N., & Popova, N. M. (2013). The role of P-glycoprotein in rational pharmacotherapy in cardiology. Rational Pharmacotherapy in Cardiology, 9(6), 701–707. https://doi.org/10.20996/1819-6446-2013-9-6-701-707
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