80岁及以上非瓣膜性心房颤动患者体内利伐沙班和钙通道阻滞剂的药物相互作用特征取决于ABCB1基因型(rs1045642和rs4148738

D. Sychev, K. Mirzaev, M. Cherniaeva, N. V. Shakhgildyan, S. Abdullaev, N. Denisenko, Z. Sozaeva, A. Kachanova, V. Shastina, S. Gorbatenkova
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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). 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摘要

背景。使用P-糖蛋白(P-gp)抑制剂和携带某些ABCB1多态性可导致利伐沙班浓度升高和出血。以维拉帕米(P-gp抑制剂)和氨氯地平为例,研究80岁以上非瓣膜性心房颤动患者体内利伐沙班的药物相互作用(DDI)特征取决于ABCB1基因型(rs1045642和rs4148738)。研究对象为 128 名患者(中位年龄为 87.5 [83-90] 岁)。对患者进行了基因分型、利伐沙班最低平衡浓度(Cmin, ss)测定和每日剂量(Cmin, ss/D)标准化、凝血图和临床相关非大出血(CRNM)医疗文件分析。根据ABCB1基因型对CRNM进行分析。与未服用钙通道阻滞剂(CCBs)的患者相比,使用利伐沙班和维拉帕米会导致CC基因型(rs1045642、rs4148738)患者的Cmin、ss值升高;CT基因型(rs1045642)中的Сmin, ss和Сmin, ss/D;CC基因型(rs1045642)中的凝血酶原时间;TT基因型(rs1045642,rs4148738)中的CRNM发生率更高。与服用氨氯地平的患者相比,CT 基因型(rs1045642)患者的 Cmin、ss 值偏高,TT 基因型(rs1045642、rs4148738)患者的 CRNM 发生率更高。与未服用氯苯类药物的患者相比,使用利伐沙班和氨氯地平会导致 CC 基因型(rs1045642)患者的 Cmin、ss 和 Cmin、ss/D 值升高(p < 0.017)。ABCB1 TT携带者(rs4148738和rs4148738)服用维拉帕米和利伐沙班分别导致75%和78%的病例发生CRNM。对于服用利伐沙班的患者,建议在治疗中加入 P-gp 抑制剂之前检测 ABCB1 基因型(rs4148738 和 rs4148738)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
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.
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