拜瑞妥
达比加群
药物遗传学
医学
CYP2D6型
CYP2C19型
单核苷酸多态性
内科学
心房颤动
华法林
基因
基因型
遗传学
生物
细胞色素P450
新陈代谢
作者
К. Б. Мирзаев,Dmitriy V. Ivashchenko,Ilya V. Volodin,Е. А. Гришина,К. А. Акмалова,А. А. Качанова,А. И. Скрипка,Radik Minnigulov,Т. Е. Морозова,О. А. Батурина,А. Н. Леванов,Tatiana Shelekhova,Alexey I. Kalinkin,Д. А. Напалков,А. А. Соколова,Д. А. Андреев,I. N. Sychev,П. О. Бочков,Д. А. Сычев
标识
DOI:10.20996/1819-6446-2020-10-05
摘要
Aim . To search for new pharmacogenetic biomarkers of bleeding risk in patients taking rivaroxaban and dabigatran for different indications: atrial fibrillation, endoprosthesis of large joints of lower limbs. Material and methods . The study enrolled 29 patients (17 patients received dabigatran and 12 –rivaroxaban), who had hemorrhagic complications during taking direct oral anticoagulants. To find new pharmacogenetic biomarkers of bleeding risk, a next generation sequencing (NGS) was performed for selected candidate genes. Results . Among the patients with bleeding who received dabigatran, 13 variants of the nucleotide sequence showed statistically significant deviation from the population values: 11 in the CES1 gene and 2 in the ABCB1 gene. Among the patients with bleeding who received rivaroxaban, 7 variants of nucleotide sequence showed significant deviation: 4 in the ABCG2 gene, 2 in the CYP3A4 gene, and 1 in the ABCB1 gene. Conclusion . The identified in this study polymorphisms of candidate genes ABCB1, ABCG2, CES1, CYP3A4 were associated with the risk of bleeding in patients taking rivaroxaban and dabigatran. It makes an important contribution to the pharmacogenetics of direct oral anticoagulants and require additional assessment of clinical significance in further studies.
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