Effects of ABCG2 421C > A genetic polymorphism on the pharmacokinetics of rivaroxaban in healthy Chinese subjects

The main objective of this study is to investigate whether the CYP3A4/5 and ABC transporter genetic polymorphisms could affect the pharmacokinetics (PK) of rivaroxaban in Chinese healthy subjects.Forty-two healthy subjects in China were recruited and given a single dose of 2.5 mg rivaroxaban tablets...

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Vydané v:Xenobiotica Ročník 55; číslo 6; s. 445 - 453
Hlavní autori: Guo, Lingfang, Sun, Xue, Bo, Qiu, Bai, Wanjun, Du, Yabin, Song, Haojing
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England 03.07.2025
Predmet:
Adult
ATP Binding Cassette Transporter, Subfamily G, Member 2 - genetics
ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism
China
East Asian People - genetics
Female
Genotype
Healthy Volunteers
Humans
Male
Multidrug Resistance-Associated Protein 2
Neoplasm Proteins - genetics
Polymorphism, Genetic
Polymorphism, Single Nucleotide - genetics
Rivaroxaban - pharmacokinetics
China
ABCG2 421C > A
pharmacokinetics
Rivaroxaban
genetic polymorphism
ISSN:0049-8254, 1366-5928, 1366-5928
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Shrnutí:The main objective of this study is to investigate whether the CYP3A4/5 and ABC transporter genetic polymorphisms could affect the pharmacokinetics (PK) of rivaroxaban in Chinese healthy subjects.Forty-two healthy subjects in China were recruited and given a single dose of 2.5 mg rivaroxaban tablets. Plasma concentration of rivaroxaban was determined by UPLC-MS/MS, the CYP3A4 20230 G > A(*1G)), CYP3A5 6986 A > G(*3), ABCB1 1236 C > T, ABCB1 3435 C > T, ABCB1 2677 G > T/A, ABCG2 34 G > A, ABCC2 1249 G > A, ABCC2 3972 C > T, ABCC2 - 24 C > T, ABCG2 421 C > A, SLC22A8 715 C > T, SLC22A8 445 C > A, SLC22A8 779 T > G, SLC22A8 829 C > T, and SLC22A8 913 A > T genotypes were determined by SnapShot Technique.In the study, compared with the subjects with C/C of ABCG2 421 C > A genotype, individuals with C/A and A/A genotype showed higher the area under the concentration-time curve AUC (289.17 358.56 439.26 ng/h/mL) (  < 0.05 and  < 0.01, respectively), AUC (293.92 362.80 442.25 ng/h/mL) (  < 0.05 and  < 0.01, respectively) and the maximum plasma concentration (56.58 70.36 83.90 ng/mL) (  < 0.05 and  < 0.01, respectively), but lower apparent clearance CL/F (9114.00 7493.82 6017.75 mL/h) (  < 0.05). Following Bonferroni correction, subjects carrying the A/A genotype continued to exhibit statistically significant differences in PK parameters , AUC , and AUC compared to C/C allele carriers.Data in the article proved that the ABCG2 421 C > A polymorphism was significantly related to the PK variability of rivaroxaban.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0049-8254
1366-5928
1366-5928
DOI:10.1080/00498254.2025.2522731