Evidence map›Paper›PMID 39619611›Full record

ArticleFrontiers in pharmacology2024

Population pharmacokinetic study of the effect of polymorphisms in the ABCB1 and CES1 genes on the pharmacokinetics of dabigatran.

Zhuan Yang, Wen Rui Tan, Qin Li, Ying Wang, Shijing Liu, Lu Chen, Yan Zhou, Chen Zeng, Yan Zeng, Yun Xiong and 6 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

16 authors.

Zhuan YangClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Wen Rui TanDepartment of Pharmacology and System Physiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Qin LiClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Ying WangClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Shijing LiuClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Lu ChenClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yan ZhouClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Chen ZengClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yan ZengClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yun XiongClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Qian ZhangClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Na LiClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Peng DuClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Lin LiuClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Jiyu ChenClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yan HeClinical Trials Center, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The impact of genetic polymorphisms in the ABCB1 and CES1 genes on dabigatran plasma concentrations remains a subject of debate, and the purpose of this study was to quantitatively assess the effects of genetic polymorphisms on dabigatran esters in healthy Chinese subjects employed a population pharmacokinetic (PopPK) approach. Methods: In total, 1,926 pharmacokinetic (PK) samples from 123 healthy individuals who were given 150 mg of dabigatran orally during a fasting state or postprandially were analyzed using the PopPK model. A two-compartment model with first-order absorption was found to adequately describe the PK data. Results: The results showed that covariates food intake and ABCB1 SNP rs4148738 were shown to have statistically significant impacts. Specifically, in postprandial administration increased lag time (ALAG) and clearance (CL) by 2.65% and 0.51%, respectively, and decreased absorption rate constant (KA) by 0.24%. Additionally, in subjects with CT genotype ABCB1 (rs4148738), the central ventricular volume of distribution (V Conclusion: In summary, the PopPK model developed in this study was robust and effectively characterized the pharmacokinetics of dabigatran in healthy Chinese adults, demonstrating that both food and ABCB1 genetic variation significantly influence the absorption and plasma concentration levels of dabigatran.

Indexed as

ABCB1CES1dabigatranfood effectsgenetic polymorphismpopulation pharmacokinetic

Identifiers

PMID39619611
PMCPMC11605329

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.