Preview

Acta Biomedica Scientifica

Advanced search

Features of drug-drug interactions rivaroxaban and calcium channel blockers depending on the ABCB1 genotype (rs1045642 and rs4148738) in patients 80 years of age and older with non-valvular atrial fibrillation

https://doi.org/10.29413/ABS.2023-8.6.6

Abstract

Background. The use of P-glycoprotein (P-gp) inhibitors and carriage of certain ABCB1 polymorphisms can lead to increased concentrations of rivaroxaban and the development of bleeding.

The aim of the study. To study the features of drug-drug interactions (DDI) of rivaroxaban in patients over 80 years of age with non-valvular atrial fibrillation depending on the ABCB1 genotype (rs1045642 and rs4148738) using the example of verapamil (P-gp inhibitor) and amlodipine.

Materials and methods. One hundred and twenty-eight patients were examined (median age – 87.5 [83–90] years). Genotyping, determination of the minimum equilibrium concentration of rivaroxaban (Cmin, ss), with standardization for the daily dose (Cmin, ss/D), coagulogram and analysis of medical documentation for the presence of clinically relevant non-major bleeding (CRNM) were carried out. Analysis of CRNM was performed depending on the ABCB1 genotype.

Results. The use of rivaroxaban with verapamil in comparison with patients not taking calcium channel blockers (CCBs) leads to high Cmin, ss values in the CC genotype (rs1045642, rs4148738); Сmin, ss and Сmin, ss/D in the CT genotype (rs1045642); prothrombin time in the CC genotype (rs1045642), more frequent occurrence of CRNM in the TT  genotype (rs1045642, rs4148738). In  comparison with patients taking amlodipine, it leads to high Cmin, ss values in the CT genotype (rs1045642), a more frequent occurrence of CRNM in the TT genotype (rs1045642, rs4148738). The use of rivaroxaban with amlodipine in comparison with patients not taking CCBs leads to high Cmin, ss and Cmin, ss/D values in the CC genotype (rs1045642) (p < 0.017).

Conclusion. The use of verapamil with rivaroxaban in ABCB1 TT carriers (rs4148738 and rs4148738) leads to the development of CRNM in 75 and 78 % of cases, respectively. In  patients taking rivaroxaban, it is advisable to test the ABCB1 genotype (rs4148738 and rs4148738) before adding a P-gp inhibitor to therapy.

About the Authors

D. A. Sychev
Russian Medical Academy of Continuous Professional Education
Russian Federation

Dmitry A. Sychev – Dr. Sc. (Med.), Professor, Professor of the RAS, Member of the RAS, Honored Scientist of the Russian Federation, Head of the Academician B.E. Votchal Department of Clinical Pharmacology and General Medicine, Rector 

Barrikadnaya str. 2/1, building 1, Moscow 125993



K. B. Mirzaev
Russian Medical Academy of Continuous Professional Education
Russian Federation

Karin B. Mirzaev – Dr. Sc. (Med.), Vice Rector for Science and Innovation 

Barrikadnaya str. 2/1, building 1, Moscow 125993



M. S. Cherniaeva
Central State Medical Academy of the Administrative Directorate of the President of the Russian Federation; War Veterans Hospital No. 2 of the Department of Health Services of Moscow
Russian Federation

Marina S. Cherniaeva – Cand. Sc. (Med.), Associate Professor at the Department of Internal Diseases and Preventive Medicine; Head of the Department of Geriatrics, Geriatrician, General Physician 

Marshala Timoshenko str. 19, building 1A, Moscow 121359;
Volgogradskiy Ave. 168, Moscow 109472



N. V. Shakhgildyan
Lomonosov Moscow State University
Russian Federation

Nataliia V. Shakhgildian – Resident Physician 

Leninskie Gory str. 1, Moscow 119991



Sh. P. Abdullaev
Russian Medical Academy of Continuous Professional Education
Russian Federation

Sherzod P. Abdullaev – Cand. Sc. (Biol.), Head of the Department of Predictive and Prognostic Biomarkers, Research Institute for Molecular and Personalized Medicine 

Barrikadnaya str. 2/1, building 1, Moscow 125993



N. P. Denisenko
Russian Medical Academy of Continuous Professional Education
Russian Federation

Natalia P. Denisenko – Cand. Sc. (Med.), Deputy Director, Research Institute for Molecular and Personalized Medicine, Associate Professor at the Academician B.E. Votchal Department of Clinical Pharmacology and General Medicine 

Barrikadnaya str. 2/1, building 1, Moscow 125993



Zh. A. Sozaeva
Russian Medical Academy of Continuous Professional Education
Russian Federation

Zhannet A. Sozaeva – Junior Research Officer at the Department of Predictive and Prognostic Biomarkers, Research Institute for Molecular and Personalized Medicine 

Barrikadnaya str. 2/1, building 1, Moscow 125993



A. A. Kachanova
Russian Medical Academy of Continuous Professional Education
Russian Federation

Anastasia A. Kachanova – Junior Research Officer at the Department of Predictive and Prognostic Biomarkers, Research Institute for Molecular and Personalized Medicine 

Barrikadnaya str. 2/1, building 1, Moscow 125993



V. R. Shastina
War Veterans Hospital No. 2 of the Department of Health Services of Moscow; I.M. Sechenov First Moscow State Medical University (Sechenov University)
Russian Federation

Vera R. Shastina – Cand. Sc. (Med.), Associate Professor at the Department of N.A. Semashko Department for Public Health and Healthcare; Chief Physician 

Volgogradskiy Ave. 168, Moscow 109472;
Trubetskaya str. 8, building 2, Moscow 119991



S. V. Gorbatenkova
War Veterans Hospital No. 2 of the Department of Health Services of Moscow
Russian Federation

Svetlana V. Gorbatenkova – Cand. Sc. (Med.), Deputy Chief Physician for Medicine 

Volgogradskiy Ave. 168, Moscow 109472



References

1. Burnett A, Mahan C, Vazquez S, Oertel L, Garcia D, Ansell J. Guidance for the practical management of the direct oral anticoagulants (DOACs) in VTE treatment. J Thromb Thrombolysis. 2016; 41(1): 206-232. doi: 10.1007/s11239-015-1310-7

2. Vazquez S. Drug-drug interactions in an era of multiple anticoagulants: a focus on clinically relevant drug interactions. Blood. 2018; 132(21): 2230-2239. doi: 10.1182/blood-2018-06-848747

3. Wieland E, Shipkova M. Pharmacokinetic and pharmacodynamic drug monitoring of direct acting oral anticoagulants: Where do we stand? Therapeutic Drug Monitoring. 2019; 41(2): 180-191. doi: 10.1097/FTD.0000000000000594

4. Sychev D, Mirzaev K, Cherniaeva M, Kulikova M, Bochkov P, Shevchenko R, et al. Drug-drug interaction of rivaroxaban and calcium channel blockers in patients aged 80 years and older with nonvalvular atrial fibrillation. Drug Metab Pers Ther. 2020; 35(3). doi: 10.1515/dmpt-2020-0127

5. Sakaeda T, Nakamura T, Okumura K. Pharmacogenetics of MDR1 and its impact on the pharmacokinetics and pharmacodynamics of drugs. Pharmacogenomics. 2003; 4: 397-410. doi: 10.1517/phgs.4.4.397.22747

6. Hoffmeyer S, Burk O, von Richter O, Arnold HP, Brockmöller J, Johne A, et al. Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci USА. 2000; 97: 3473-3478. doi: 10.1073/pnas.97.7.3473.36

7. Kimchi-Sarfaty C, Oh J, Kim I-W, Sauna Z, Calcagno A, Ambudkar S, et al. “Silent” polymorphism in the MDR1 gene changes substrate specificity. Science. 2007; 315(5811): 525-528. doi: 10.1126/science.1135308

8. Fung K, Pan J, Ohnuma S, Lund P, Pixley J, Kimchi-Sarfaty C, et al. MDR1 synonymous polymorphisms alter transporter specificity and protein stability in a stable epithelial monolayer. Cancer Res. 2014; 74: 598-608. doi: 10.1158/0008-5472

9. Kanuri H, Kreutz R. Pharmacogenomics of novel direct oral anticoagulants: Newly identified genes and genetic variants. J Pers Med. 2019; 9(1): 7. doi: 10.3390/jpm9010007

10. Ing Lorenzini K, Daali Y, Fontana P, Desmeules J, Samer C. Rivaroxaban-induced hemorrhage associated with ABCB1 genetic defect. Front Pharmacol. 2016; 7: 494. doi: 10.3389/fphar.2016.00494

11. Cullell N, Carrera C, Muino E, Torres N, Krupinski J, Fernandez-Cadenas I. Pharmacogenetic studies with oral anticoagulants. Genome-wide association studies in vitamin K antagonist and direct oral anticoagulants. Oncotarget. 2018; 9: 29238-29258. doi: 10.18632/oncotarget.25579

12. Wolking S, Schaeffeler E, Lerche H, Schwab M, Nies A. Impact of genetic polymorphisms of ABCB1 (MDR1, P-glycoprotein) on drug disposition and potential clinical implications: Update of the literature. Clin Pharmacokinet. 2015; 54: 709-735. doi: 10.1007/s40262-015-0267-1

13. Gouin-Thibault I, Delavenne X, Blanchard A, Siguret V, Salem JE, Narjoz C, et al. Interindividual variability in dabigatran and rivaroxaban exposure: Contribution of ABCB1 genetic polymorphisms and interaction with clarithromycin. J Thromb Haemost. 2017; 15: 273-283. doi: 10.1111/jth.13577

14. Sychev D, Ostroumova O, Cherniaeva M, Shakhgildian N, Mirzaev K, Abdullaev S, et al. The influence of ABCB1 (rs1045642 and rs4148738) gene polymorphisms on rivaroxaban pharmacokinetics in patients aged 80 years and older with nonvalvular atrial fibrillation. High Blood Press Cardiovasc Prev. 2022; 29(5): 469-480. doi: 10.1007/s40292-022-00536-3

15. Kaatz S, Ahmad D, Spyropoulos A, Schulman S; Subcommittee on Control of Anticoagulation. Definition of clinically relevant non-major bleeding in studies of anticoagulants in atrial fibrillation and venous thromboembolic disease in non-surgical patients: Communication from the SSC of the ISTH. J Thromb Haemost. 2015; 13: 2119-2126. doi: 10.1111/jth.13140

16. Schulman S, Kearon C; Subcommittee on Control of Anticoagulation of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Definition of major bleeding in clinical investigations of antihemostatic medicinal products in non-surgical patients. J Thromb Haemost. 2005; 3: 692-694. doi: 10.1111/j.1538-7836.2005.01204.x

17. Levey A, Stevens L, Schmid C, Zhang Y, Castro A 3rd, Feldman H, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009; 150: 604-612. doi: 10.7326/0003-4819-150-9-200905050-00006

18. Narkevich AN, Vinogradov KA, Grjibovskii AM. Multiple comparisons in biomedical research: The problem and its solutions. Human Ecology. 2020; 27(10): 55-64. (In Russ.). doi: 10.33396/1728-0869-2020-10-55-64

19. Arutyunov GP, Fomin IV, Tarlovskaya EI, Arutyunov AG, Alyavi AL, Vishlov EV, et al. An algorithm for assessing and modifying risk factors for minor bleeding in patients with atrial fibrillation receiving DOAC therapy: Resolution of the Eurasian Association of Therapists. 2019. (In Russ.). URL: https://euat.ru/upload/recommendation/1673341858.pdf [дата доступа: 01.06.2023].

20. Benign prostatic hyperplasia: Clinical guidelines. Moscow; 2020. (In Russ.).

21. Lorenzini K, Daali Y, Fontana P, Desmeules J, Samer C. Rivaroxaban-induced hemorrhage associated with ABCB1 genetic defect. Front Pharmacol. 2016; 7: 494. doi: 10.3389/fphar.2016.00494

22. Sennesael A, Larock A, Douxfils J, Elens L, Stillemans G, Wiesen M, et al. Rivaroxaban plasma levels in patients admitted for bleeding events: Insights from a prospective study. Thromb J. 2018; 16: 28. doi: 10.1186/s12959-018-0183-3

23. Gouin-Thibault I, Delavenne X, Blanchard A, Siguret V, Salem J, Narjoz C, et al. Interindividual variability in dabigatran and rivaroxaban exposure: Contribution of ABCB1 genetic polymorphisms and interaction with clarithromycin. J Thromb Haemost. 2017; 15(2): 273-283. doi: 10.1111/jth.13577

24. Pham P, Schmidt S, Lesko L, Lip G, Brown J. Association of oral anticoagulants and verapamil or diltiazem with adverse bleeding events in patients with nonvalvular atrial fibrillation and normal kidney function. JAMA Netw Open. 2020; 3(4): e203593. doi: 10.1001/jamanetworkopen.2020.3593


Review

For citations:


Sychev D.A., Mirzaev K.B., Cherniaeva M.S., Shakhgildyan N.V., Abdullaev Sh.P., Denisenko N.P., Sozaeva Zh.A., Kachanova A.A., Shastina V.R., Gorbatenkova S.V. Features of drug-drug interactions rivaroxaban and calcium channel blockers depending on the ABCB1 genotype (rs1045642 and rs4148738) in patients 80 years of age and older with non-valvular atrial fibrillation. Acta Biomedica Scientifica. 2023;8(6):51-80. https://doi.org/10.29413/ABS.2023-8.6.6

Views: 393


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2541-9420 (Print)
ISSN 2587-9596 (Online)