Evidence map›Paper›PMID 40365305›Full record

ArticleFrontiers in pharmacology2025

Effect of ABCB1 SNP polymorphisms on the plasma concentrations and clinical outcomes of rivaroxaban in Chinese NVAF patients: a population pharmacokinetic-based study.

Fei Wang, Ze Li, Youqi Huang, Qin Liu, Libin Zhao, Honghong Wang, Hongjin Gao, Mingyu Chen, Yuze Lin, Xingang Li and 1 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Fei Wang *Department of Pharmacy, Fujian Provincial Geriatric Hospital, Clinical College of Fujian Medical University, Fuzhou, China.
Ze Li *Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Youqi Huang *Shengli Clinical College of Fujian Medical University, School of Pharmacy, Fujian Medical University, Fuzhou, China.
Qin LiuDepartment of Pharmacy, Fujian Provincial Geriatric Hospital, Clinical College of Fujian Medical University, Fuzhou, China.
Libin ZhaoDepartment of Intensive Care Unit, Fujian Provincial Geriatric Hospital, Clinical College of Fujian Medical University, Fuzhou, China.
Honghong WangDepartment of Pharmacy, Liuzhou Maternity and Child Healthcare Hospital, Affiliated Maternity Hospital, Liuzhou, China.
Hongjin GaoShengli Clinical College of Fujian Medical University, Department of Pharmacy, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Mingyu ChenShengli Clinical College of Fujian Medical University, School of Pharmacy, Fujian Medical University, Fuzhou, China.
Yuze LinShengli Clinical College of Fujian Medical University, School of Pharmacy, Fujian Medical University, Fuzhou, China.
Xingang LiDepartment of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Min ChenShengli Clinical College of Fujian Medical University, Department of Pharmacy, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study utilized a population pharmacokinetic (PPK) approach to assess the influence of ABCB1 genetic polymorphisms on the plasma concentrations and clinical outcomes of rivaroxaban. Methods: The PPK model for rivaroxaban was developed using the nonlinear mixed-effects modelling approach and Monte Carlo simulations were employed to derive peak concentration (C Results: Analysis of 287 rivaroxaban plasma concentrations from 228 non-valvular atrial fibrillation (NVAF) patients revealed significant associations between AST (aspartate aminotransferase)/ALT (alanine aminotransferase) ratios and the apparent clearance (CL/F), the apparent volume of distribution (V/F). ABCB1 1236C>T TT and ABCB1 c.2482-2236C>T CC genotypes exhibited higher dose-adjusted C Conclusion: The PPK model incorporated CL/F and V/F with the covariate AST/ALT. Model-based simulations revealed that ABCB1 1236C>T, ABCB1 c.2482-2236C>T, and ABCB1 3435C>T genotypes had significant impacts on the plasma concentrations of rivaroxaban. Specifically, ABCB1 c.2482-2236C>T and ABCB1 3435C>T genotypes were associated with bleeding events and thromboembolic events, respectively.

Indexed as

ABCB1 genetic polymorphismsnon-valvular atrial fibrillationpopulation pharmacokineticrivaroxabanTDM (therapeutic drug monitoring)

Identifiers

PMID40365305
PMCPMC12069994

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