For more than 50 years, oral vitamin K antagonists were the choice of anticoagulant for the long-term treatment and prevention of arterial and venous thromboembolic events. In recent years, four direct oral anticoagulants (DOACs), dabigatran, rivaroxaban, apixaban and edoxaban have been compared with warfarin for thromboembolism prevention. These anticoagulants directly inhibit specific proteins within the coagulation cascade; in contrast, oral vitamin K antagonists inhibit the synthesis of vitamin K-dependent clotting factors. Dabigatran, a direct thrombin inhibitor, and rivaroxaban, apixaban and edoxaban, the factor Xa inhibitors, produce a more predictable, less labile anticoagulant effect. DOACs do not have limitations inherent vitamin K antagonists. DOACs have a predictable pharmacokinetic profile and are free of advers drugs reactions inherent in vitamin K antagonists. However, it is necessary to take into account the pharmacogenetic characteristics of the individual that can affect effectiveness and safety of use of DOACs. The results carried out to the present fundamental and clinical studies of DOACs studies demonstrate an undeniable the influence of genome changes on the pharmacokinetics and pharmacodynamics of DOACs. However, the studies need to be continued. There is a need to plan and conduct larger studies in various ethnic groups with the inclusion of sufficient associative genetic studies of the number of patients in each of the documented groups treatments with well-defined phenotypes.
- dabigatran etexilate
- single nucleotide variant
Thromboembolism (such as stroke and systemic embolism) is a serious complication of non-valvular atrial fibrillation (AF) . Pulmonary embolism (PE) can cause death within first 14 days after a stroke in 25–50% of cases . In absence of preventive measures, venous thromboembolic complications in lower limb arthroplasty (deep vein thrombosis and PE) reached 15–30% of cases before widespread use of anticoagulant therapy in clinical practice. However, with introduction of new anticoagulants in 2001, these indicators decreased to 1–2% , and in recent years-to 0.7–1.7% of . Long-term use of anticoagulants is necessary for prevention of thromboembolic complications in patients with high risk of thromboembolism. For long time, vitamin K antagonists (warfarin, acenocumarol, phenindione) and indirect thrombin inhibitors (heparins) were used as drugs to prevent occurrence of thromboembolic complications [5, 6]. However, despite its effectiveness, coumarin therapy has some limitations. Drugs of this group are characterized by delayed therapeutic effect (after 36–72 hours from start of administration, with development of maximum effect on 5–7 days from start of use) . Also, there is a need for regular therapeutic drug monitoring with the control of international normalized ratio (INR) indicator at safe level within 2–3, which entails additional economic burdens on health system . A significant disadvantage of this group of drugs is irreversibility of drug in the event of an overdose . The deviation of the INR from the permissible limits, both in lower and in higher direction, is prognostically unfavorable indicator. In first case, the therapeutic effect of anticoagulant therapy will not be achieved. In second case, the risk of hemorrhagic complications increases . Balancing the effectiveness and safety of anticoagulant therapy is a difficult task in real clinical practice. Genetically determined features of individual’s enzyme systems involved in drug metabolism make significant contribution to their effectiveness and safety . An alternative to vitamin K antagonists were direct oral anticoagulants (DOACs), which do not have limitations inherent in warfarin : dabigatran, rivaroxaban, apixaban, endoxaban. DOACs have a predictable pharmacokinetic profile and are free of disadvantages inherent in vitamin K antagonists. However, it is necessary to take into account the pharmacogenetic characteristics of the individual that can affect effectiveness and safety of use of DOACs.
Dabigatran etexilate is first DOAC that has direct reversible inhibitory effect on thrombin [13, 14]. Thrombin is catalyst for conversion of factors V, VIII and XI in blood clotting cascade, and also catalyzes conversion of fibrinogen to fibrin and factor XIII to factor XIIIa, which contributes to stabilization of fibrin . Also, thrombin activates GPCR receptors, which leads to conformational changes in platelets and promotes their aggregation. This leads to the release of even more clotting factors and the formation of more thrombin .
After entering the human body, dabigatran etexilate, being an inactive precursor (prodrug), quickly turns into an active metabolite – dabigatran. Dabigatran reversibly binds to the active center of the thrombin molecule, preventing thrombin-mediated activation of clotting factors. An important feature of dabigatran is that it can inactivate thrombin, even if it is in a bound state with fibrin . The maximum concentration (Cmax) of dabigatran in plasma and, accordingly, anticoagulant action is observed as early as 0.5–2 hours after oral administration . The half-life (T 1/2) of dabigatran with a single dose is 11 hours, but with regular intake it increases to 12–14 hours, which allows you to prescribe dabigatran etexilate 2 times a day . Approximately one-third of the dabigatran circulating in blood binds to proteins. The drug is excreted unchanged from the body: 85% - with kidneys, 15% - with bile [20, 21].
It is important that dabigatran etexilate is not metabolized by cytochrome P450 isoenzymes of liver and does not change their activity. The CES1 and CES2 enzymes are human liver carboxylesterases that hydrolyze various xenobiotics and endogenous substrates using ester or amide bonds. Conversion of dabigatran etexylate to dabigatran depends more on activity of CES1 than on activity of CES2 [22, 23, 24].
Glycoprotein P (P-gp) is an ATP-dependent transporter that is involved in transfer of substrate molecules across membranes of expressing cells and components (regardless of concentration gradient) [25, 26]. P-gp is widely present in human body tissues and plays leading role in pharmacokinetics of dabigatran etexilate, which is a substrate for P-gp . It is necessary to take into account drug interaction when prescribing dabigatran etexilate with P-gp inhibitors (verapamil, amiodarone, carvedilol, quinidine, spironolactone, nicardipine, propafenone, atorvastatin, clarithromycin, erythromycin, fluoroquinolones, ketoconazole, intraconazole, cyclosporine, fluoxetine, paroxetine, pentazocine, ritonavir, lopinavir, grapefruit juice, and others), as this leads to decrease in its effectiveness, increased absorption of these drugs, inhibition of their excretion, and increased penetration through barriers. This leads to an increase in the concentration of P-gp substrate drugs in the blood and tissues and increases the risk of adverse drug reactions (ADRs). Bernier et al. revealed development of bleeding in 30.4% of patients taking P-gp inhibitors together with dabigatran . On contrary, drugs that are inducers of P-gp (rifampicin, morphine, dexamethasone, retinoids, barbiturates, nicotine, diphenin, isoniazid, carbamazepine, caffeine, diazepam, diphenhydramine, tricyclic antidepressants, phenytoin, ethanol), when used with dabigatran, by increasing activity of P-gp, lead to inhibition of dabigatran absorption, increase its elimination and inhibition of penetration through barriers. This leads to decrease in concentration of P-gp substrate drug and a decrease in its effectiveness. It is also important to take into account that simultaneous use of substrates and P-gp inhibitors increases the risk of developing congenital anomalies in fetus .
In addition to CES1 and ABCB1, which affect biotransformation of dabigatran etexylate and the effectiveness of active dabigatran, glucuronidation enzymes UGT2B15, UGT1A9, and UGT2B7 also participate in its metabolism (elimination). Their activity reflects safety of using dabigatran . The main and most interesting enzyme involved in elimination of dabigatran is UGT2B15. When prescribing dabigatran etexilate, it is important to consider drug interactions with drugs that are metabolized by UGT2B15. By interacting competitively with enzyme, they can slow down metabolism of dabigatran (for example, acetaminophen, loratadine, lorazepam, oxazepam, morphine, valproic acid) [30, 31], and its concentration will increase, increasing the risk of ADRs.
To date, the
Gouin-Thibault et al.  evaluated effect of clarithromycin on pharmacokinetics of dabigatran in 60 healthy male volunteers selected for
The aim of the study is Shi et al.  studied effect of the ONVs of
The activity of glucuronidation enzymes depends on the ONVs of their encoding genes. To date, we have not found any works that would present studies of association of carrier of the UGT family genes on metabolism of dabigatran in humans. However, we can assume that this may change its concentration in blood plasma of patients. This hypothesis is based on previous studies of associations of ONVs carrier of
Rivaroxaban is the first direct factor Xa inhibitor. Pharmacokinetics of rivaroxaban does not have disadvantages of vitamin K antagonists. However, pharmacokinetics and pharmacogenetics of rivaroxaban are variable. This can affect both effectiveness and safety of anticoagulant therapy.
Rivaroxaban inhibits platelet activation and fibrin clot formation by direct, selective and reversible inhibition of factor Xa in both intrinsic and extrinsic coagulation pathways. Factor Xa, as part of prothrombinase complex, also composed of factor Va, calcium ions, factor II, and phospholipids, catalyzes the conversion of prothrombin to thrombin. Thrombin activates platelets and catalyzes the conversion of fibrinogen to fibrin. Thus, factor Xa is a coagulation factor that acts at point of convergence of internal and external pathways in blood coagulation system. It catalyzes the breakdown of prothrombin and is therefore critical for thrombin generation. It is important to note that rivaroxaban inhibits free prothrombinase- and clot-associated factor Xa without directly affecting platelet aggregation . This distinguishes rivaroxaban from indirect inhibitors of factor Xa, which does not inhibit factor Xa associated with prothrombinase complex .
When taken orally, rivaroxaban reaches its maximum plasma concentration after 2–4 hours. The absolute bioavailability of rivaroxaban for dosage of 10 mg is relatively high (80–100%) and does not depend on food intake [41, 42]. Under fasting conditions, oral bioavailability of rivaroxaban at dosage of 20 mg decreases to 66%. When using drugs at a dosage of 20 mg with food, the AUC increases to 39%. This indicates an almost absolute absorption and, at same time, a high oral bioavailability of rivaroxaban. The connection with plasma proteins reaches 92–95%. Because of this high plasma protein binding, rivaroxaban is not removed during dialysis .
Rivaroxaban is eliminated from body in various ways, of which three are main ones. Approximately 36% of dose is excreted unchanged by kidneys through active transporter-mediated secretion by P-glycoprotein (Pgp) and BCRP (ABCG2). In addition, 14% of dose is eliminated by hydrolysis of amide bonds and 32% of dose is eliminated via oxidative metabolic pathways. Liver isoenzymes CYP3A4 and CYP3A5 are responsible for metabolism about 18%, and CYP2J2 - about 14% of the dose [44, 45]. Level of rivaroxaban when administered concomitantly with midazolam (a CYP3A4 substrate) is reduced by an average of 11% compared with rivaroxaban alone. The following drugs moderately alter the level of rivaroxaban: erythromycin (a moderate inhibitor of CYP3A4/P-gp; an increase of 34%); clarithromycin (potent CYP3A4/mild P-gp inhibitor; 54% increase); fluconazole (moderate CYP3A4, a possible inhibitor of BCRP (ABCG2); an increase of 42%). A significant increase in blood levels and strength of action of rivaroxaban has been demonstrated when used simultaneously with drugs that are potent inhibitors of the CYP3A4 enzyme and P-gp/BCRP transporter proteins (ABCG2) and potential inhibitors of CYP2J2 enzyme, for example: use of ketoconazole 400 mg once a day leads to an increase in level of rivaroxaban by 158% (95% CI: 136% - 182%); the use of ritonavir increases level of rivaroxaban by 153% (95% CI: 134% - 174%) .
The expression of rivaroxaban transporter proteins may be influenced by SNVs of
In the study by Sychev et al. found no significant differences in peak steady-state concentration of rivaroxaban between mutant haplotypes and wild haplotypes of
Promising direction is study of BCRP protein, encoded by
Metabolism of rivaroxaban in liver is carried out by cytochrome P450 isoenzymes 3A4 (
The study of effect of a potent P-gp inhibitor cyclosporin and its combination with a moderate CYP3A inhibitor fluconazole on pharmacokinetics of rivaroxaban and CYP3A activity (compared with baseline) showed that cyclosporine increased average exposure of rivaroxaban by 47%, maximum concentration of CYP3A4 and decreased by 34%, and cyclosporine in combination with fluconazole increased the average exposure of rivaroxaban by 86% and maximum concentration by 115%. This effect was significantly stronger than that observed in control group that received rivaroxaban with fluconazole alone .
The high clinical significance of interaction of rivaroxaban with other drugs is shown in a systematic review and meta-analysis of studies in which patients with atrial fibrillation were randomized to groups taking DOACs or warfarin, stratified by number of concomitant drugs . Polypharmacy was significantly associated with poor outcomes and reduced the benefit in terms of risk of major bleeding in patients receiving rivaroxaban, especially in presence of drugs that modulate P-gp/CYP3A4.
Also, about 10 different SNVs for
Apixaban is a potent direct oral reversible and highly selective factor Xa inhibitor that does not require antithrombin III for antithrombotic activity [60, 61]. Apixaban inhibits both free and clot-associated factor Xa and prothrombinase activity, which inhibits clot growth . By inhibiting factor Xa, apixaban reduces formation of thrombin and development of blood clots. It has no direct effect on platelet aggregation, but indirectly inhibits thrombin-induced platelet aggregation .
Absorption of apixaban occurs mainly in small intestine and gradually decreases as it passes through it . For oral doses up to 10 mg, absolute bioavailability of apixaban is about 50% due to incomplete absorption [65, 66] and first passage through liver [67, 68]. Apixaban Cmax in plasma is reached 3–4 hours after oral administration [69, 70]. Binding of apixaban to blood plasma proteins, mainly albumin, is about 87% . After oral administration, unchanged apixaban is main drug component in human blood plasma without presence of active circulating metabolites . Excretion of apixaban involves several pathways, including metabolism in liver, as well as excretion by unchanged parent compound in bile and kidneys, and direct intestinal excretion .
Metabolic pathways of apixaban include O-demethylation, hydroxylation, and sulfation of hydroxylated O-demethylapixaban . At same time, metabolism mainly occurs through isoenzymes CYP3A4 /5 of liver cytochrome P450, with an insignificant participation of isoenzymes CYP1A2, CYP2C8, CYP2C9, CYP2C19 and CYP2J2 .
The role of non-functional allele G (rs776746) of
The highest risk of developing apixaban-induced ADRs due to a slowdown in the metabolism of drug in liver, especially when combined with drugs-inhibitors of CYP3A5 isoenzyme, in homozygous carriers of non-functional alleles CYP3A5*2 (rs28365083), CYP3A5*3 (rs776746), CYP3A5*6 (rs10264272), CYP3A5*7 (rs41303343), CYP3A5*8 (rs55817950), CYP3A5*9 (rs28383479), CYP3A5*10 или CYP3A5*3 K (rs41279854), CYP3A5*11 (rs72552791), CYP3A5*3D (rs56244447), CYP3A5*3F (rs28365085), CYP3A5_3705C > T(H30Y) (rs28383468), CYP3A5_7298C > A(S100Y) (rs41279857). Among them, the most common is non-functional allele CYP3A5*3 (rs776746). In terms of phenotypes, individuals are “expressors” of CYP3A5 if they carry at least one CYP3A5*1 allele, and “non-expressors” if not. It should be noted that frequency of carriage of SNVs of CYP3A5 gene varies significantly depending on ethnicity of patients. For example, most Europeans are not expressors, while many people of African descent are CYP3A5 expressors [63, 74]. Higher concentrations of active component of drugs, metabolized with participation of isoenzyme CYP3A5, in blood plasma are higher in non-expressors of CYP3A5 compared with expressors . In patients belonging to group of non-expressing CYP3A5 (homozygous carriers of the above non-functional alleles), apixaban dosing should be cautious and requires monitoring of ADRs. Co-administration of apixaban with other drugs metabolized with participation of CYP3A5 isoenzyme should be avoided in non-expressors,
The study SNVs of CYP3A5 gene was conducted among 200 postmenopausal women who had an episode of venous thromboembolism and more than 500 comparable control groups. It is known that oral estrogen intake increases the risk of venous thromboembolism in all women (odds ratio (OR) - 4.5; CI: 2.6–7). Compared with women who did not receive oral estrogens, the OR for venous thromboembolism in users of oral estrogens was 3.8 (CI: 2.1–6.7) among women who did not have the common (wild) CYP3A5 * 1 allele encoding a highly functional isoenzyme CYP3A5, and 30.0 (CI: 4.4–202.9) among patients with this allele (interaction test p = 0.04) . This is important to consider when prescribing apixaban to postmenopausal women.
Carriage of low-functional alleles CYP1A2*1C (rs2069514), CYP1A2*1K_-729C > T (rs12720461), CYP1A2*1K_-739 T > G (rs2069526), CYP1A2*3 (rs56276452), CYP1A2*4A (rs56276455), CYP1A*4A (rs28399424) of
Carriers of SNVs of
Some of major metabolic pathways of apixaban include o-demethylation, hydroxylation, and sulfation, with o-demethylapixaban sulfate being main metabolite . Potentially important pharmacogenomic metabolic pathway is via sulfotransferases (SULT) SULT1A1 and SULT1A2, which are responsible for sulfation of o-demethyl-apixaban to o-demethyl-apixaban sulfate [79, 80]. SULT1A1 enzyme is more efficient than SULT1A2 in sulfation of o-demethyl-apixaban . O-demethyl-apixaban is the most well-known metabolite and accounts for 25% of the estimated active apixaban . It is important to know that o-demethyl-apixaban sulfate does not have any inhibitory activity against factor Xa, which may contribute to anticoagulant efficacy of apixaban . Three important SNVs of
Edoxaban is a selective, direct and reversible inhibitor of activated blood coagulation factor X (F Xa), a serine protease responsible for thrombin formation. Edoxaban is used to prevent stroke in nonvalvular AF, treat deep vein thrombosis and PE [84, 85, 86].
It binds to both free FXa and free FXa in prothrombinase complex, thus causing a dose-dependent decrease in thrombin formation .
Edoxaban is characterized by linear, predictable pharmacokinetic profile . After oral administration, edoxaban reaches peak plasma concentrations (C max) within 1–2 hours . The half-life (T1/2) of edoxaban is approximately 10–14 hours . Edoxaban is absorbed mainly in upper gastrointestinal tract, approximately 13% is absorbed in large intestine .
In an in vitro study, five phase 1 metabolites of edoxaban were found in human liver microsomes: M-1, M-4, M-5, M-6 and a hydroxylated metabolite at the N-dimethylcarbamoyl group of edoxaban (hydroxymethylenedoxaban) (M-7) . Formation of a metabolite M-4, unique for humans, is catalyzed by CES1, which is present in human liver microsomes and in the cytosol. Cytochrome P450 (CYP) 3A4 isoenzyme mediates formation of M-5 and hydroxymethylenedoxaban in presence of nicotinamide adenine dinucleotide phosphate (NADPH). It is assumed that M-8, minor metabolite, arises spontaneously (non-enzymatically) via an intermediary, hydroxymethylenedoxaban, which is formed via CYP3A4/5 .
Second phase of edoxaban metabolism is mediated by glucuronidation to form N-glucuronide metabolite (M-3). This metabolite has not been quantified. Three metabolites (M-4, M-6 and M-8) have anticoagulant activity with half-maximum inhibitory concentration (IC50) values for anti-FXa 1.8 nM (M-4), 6.9 nM (M-6) and 2.7 nM (M-8). The IC 50 value of edoxaban for anti-FXa is 3 nM . However, due to its low content and high protein binding (80%), it is expected that most abundant metabolite M-4 will not make a significant contribution to overall pharmacological activity of edoxaban in patients with at least a moderate decline in renal function . Other metabolites are present in even smaller amounts and (in the absence of liver cytochrome P450 inducers) do not significantly contribute to total anticoagulant activity of drugs. None of metabolic pathways alone contributes more than 10% to total clearance of edoxoban .
Edoxaban is a substrate for P-gp and is not a substrate for other transporters such as anion transport polypeptide (OATPs), 1B1, or organic cation transporters (OATs) 2 .
Edoxaban is mainly excreted unchanged in urine and through the secretion of biliary tract with feces . Renal clearance of unchanged drugs is approximately 50% of total clearance, and remaining 50% of non-renal clearance occurs due to metabolism and secretion of the biliary tract. As previously described, edoxaban is metabolized by the enzymes CES1 (<10%), CYP3A4 (<10%) and by glucuronidation; but metabolism is a minor route of elimination of edoxaban in patients with normal renal function. Therefore, inhibitors or inducers of these enzymes are unlikely to have clinically significant interactions with edoxaban. However, drug interaction studies have been performed to investigate the effect of CYP3A4 inhibitors on the pharmacokinetics of edoxaban. In addition, the effects of other drugs that could be administered concurrently with edoxaban were evaluated. Since edoxaban is a substrate of the P-gp efflux transporter, several studies have been carried out on interaction of drugs with inhibitors, substrates and inducers of P-gp. The effect of co-administration of P-gp inhibitors was an increase in effect of edoxaban (maximum observed drug concentration in plasma C max and area under the curve of concentration versus time AUC), but the increase was less than 2 times. P-gp inhibitors and potent CYP3A4 / 5 inhibitors (eg, ketoconazole, erythromycin) do not result in greater increases in exposure compared to mild P-gp inhibitors (eg verapamil) or mild inhibitors (eg cyclosporine) CYP3A4 / 5. This confirms that the metabolism of CYP3A4/5 is not the main route of elimination of edoxaban [96, 97].
Сo-administration of ketoconazole (P-gp inhibitor; potent CYP3A4 inhibitor) increased the single dose peak and overall exposure to edoxaban by 89% and 87%, respectively . However, co-administration of oral quinidine (P-gp and OCT2 transporter inhibitor; potent CYP2D6 inhibitor) increased the single dose peak and 24-hour exposure of oral edoxaban by 85% and 77%, respectively .
Co-administration of sustained-release verapamil (P-gp inhibitor (main effect); moderate CYP3A4 inhibitor) increased the peak and 24-hour exposure of single doses of edoxaban by 53% .
Co-administration of erythromycin (P-gp inhibitor; moderate CYP3A4 inhibitor) increased the peak and total exposure of single doses of edoxaban by 68% and 85%, respectively . Co-administration of cyclosporine (P-gp inhibitor, OATP1B1 and BCRP; weak inhibitor of CYP3A4) increased both the peak and total exposure of single doses of edoxaban by 74% and 73%, respectively . Co-administration of dronedarone (a P-gp inhibitor) increased the peak and total exposure of single doses of edoxaban by 46% and 85%, respectively .
The administration of amiodarone (P-gp inhibitor; moderate CYP2C9 inhibitor, weak CYP2D6 inhibitor) to patients receiving edoxaban for 3 days of once daily administration increased the peak and total exposure of single doses of edoxaban by 66% and 40%, respectively . This is important to remember because amiodarone has a long half-life, reaching an average of 58 days . Rifampicin, inducer of P-gp (strong CYP3A4 inducer; moderate inducer of CYP2B6, 2C8, 2C9, 2C19; inhibitor of P-gp, OATP1B1, OATP1B3) after 7 days of dosing reduced the total exposure to edoxaban by about 34%, without affecting its peak exposure . Co-administration of digoxin (P-gp substrate) increased the C max of edoxaban by 16% without significantly affecting overall exposure or renal clearance at steady state .
At the same time, atorvastatin (OATP1B1 and OATP1B3 substrate; weak CYP3A4 inhibitor), when taken together with edoxaban, does not affect the peak or total exposure of edoxaban . Co-administration of naproxen and edoxaban also had no effect on the peak and total exposure of edoxaban. However, led to an increase in the duration of bleeding compared with each drug administered separately. Co-administration of naproxen increased the baseline-adjusted bleeding time ratio by 72% on day 2 compared with edoxaban alone (90% CI: 139.3–213.3). In contrast, concomitant administration of edoxaban with naproxen increased the equivalent bleeding time by 22% compared with naproxen alone (90% CI: 98.1–151.0) . Naproxen reduced the baseline-adjusted platelet aggregation coefficient on the 2nd day of co-administration by 69.89% (90% CI: 68.20–71.62), while edoxaban itself did not affect platelet aggregation.
Co-administration of high doses of aspirin (325 mg) increased the stationary peak and total exposure of edoxaban by 34% and 30%, respectively, and decreased renal clearance by 17%, possibly due to inhibition of active renal secretion. Co-administration of low-dose aspirin (100 mg) did not affect the peak or total exposure of edoxaban either after a single dose or with stable use (90% CI: 80–125%). Co-administration of edoxaban and aspirin at low (100 mg) or high (325 mg) doses resulted in an additive effect in terms of increased bleeding time. The anticoagulant effects of edoxaban were not affected by the simultaneous administration of aspirin. Coadministration of low doses of aspirin (100 mg) did not significantly affect INR, prothrombin time (PTI), activated partial thromboplastin time (APTT), or intrinsic FXa activity . Enoxaparin did not affect the peak and total exposure of edoxaban with simultaneous dosing or with an interval of 12 hours. Co-administration of edoxaban at a dose of 60 mg and subcutaneous enoxaparin at a dose of 1 mg/kg led to an increase in the effect on the parameters of the analysis of thrombin formation compared to any of the drugs introduced separately. The effect was generally not additive, with the exception of the delay in thrombin formation and the time to peak. The effect on anti-FXa with the simultaneous use of both drugs was additive .
Edoxaban and its active metabolite M4 are substrates for P-gp encoded by
Only a limited amount of edoxaban is metabolized by liver cytochrome P450 isoenzymes (less than 4%) . Metabolites M4 and M1 are formed during the hydrolysis of edoxaban with the participation of the CES1 enzyme encoded by
There is probably a high risk of developing edoxaban-induced adverse reactions due to a slowdown in the metabolism of the drug in the liver when combined with drug inhibitors of the CYP3A5 isoenzyme in homozygous carriers of non-functional alleles
The results carried out to the present fundamental and clinical studies of DOACs studies demonstrate an undeniable the influence of genome changes on the pharmacokinetics and pharmacodynamics of DOACs. However, the studies need to be continued. There is a need to plan and conduct larger studies in various ethnic groups with the inclusion of sufficient associative genetic studies of the number of patients in each of the documented groups treatments with well-defined phenotypes. Additional work needed to translation of research results into real clinical practice using results of pharmacogenetic testing and taking into account genomic variations for selection DOACs, their starting and target dosages, which is especially important when the need for long-term pharmacotherapy.