Evidence map›Paper›PMID 42220444›Full record

ArticleTherapeutic advances in drug safety2026

Pharmacogenetic variants in pharmacokinetic and pharmacodynamic pathways and clinical factors associated with bleeding risk in Thai patients receiving rivaroxaban: a case-control study.

Varalee Yodsurang, Krit Wattanathum, Thanate Srimatimanon, Krittin Pitinanon, Andro Ranti, Pattaraporn Siripattarachai, Piyapha Hirunpatrawong, Voravut Rungpradubvong, Seiichi Sakamoto, Alisara Sangviroon Sujarit

Abstract read
In one paragraph

Article in Therapeutic advances in drug safety, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Varalee YodsurangDepartment of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-3622-532X
Krit WattanathumDepartment of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand.ORCID https://orcid.org/0009-0001-9807-3333
Thanate SrimatimanonDepartment of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0009-0008-1724-9028
Krittin PitinanonDepartment of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0009-0006-6783-8547
Andro RantiDepartment of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0009-0004-0096-8246
Pattaraporn SiripattarachaiDepartment of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0009-0004-3872-3260
Piyapha HirunpatrawongDepartment of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-4803-8046
Voravut RungpradubvongDivision of Cardiovascular Medicine, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-3661-1490
Seiichi SakamotoGraduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID https://orcid.org/0000-0001-6871-522X
Alisara Sangviroon SujaritDepartment of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Chulalongkorn University, 254 Pathumwan, Bangkok 10330, Thailand.ORCID https://orcid.org/0009-0000-6297-8782

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: While bleeding is an inherent risk of all anticoagulant therapies, individual susceptibility varies considerably. Rivaroxaban, a direct oral anticoagulant widely used for thromboembolic prevention, is associated with substantial interindividual variability in bleeding risk, posing an ongoing clinical challenge. Objectives: To investigate associations between pharmacogenetic variants in five pharmacokinetic (PK) and nine pharmacodynamic (PD) genes, along with clinical factors, and bleeding outcomes in Thai patients receiving rivaroxaban. Design: A retrospective case-control study was conducted among 91 patients with atrial fibrillation, including 27 who experienced bleeding events. Methods: Genetic variants in PK and PD genes were genotyped using the MassARRAY Results: The CT genotype of Conclusion: Bleeding risk in Thai patients receiving rivaroxaban appeared to be influenced by both pharmacogenetic variants, particularly the Trial registration: As a retrospective non-interventional study, this work was not registered in a clinical trial registry. Ethical approval was obtained (COA No. 1657/2022).

Indexed as

bleedingpharmacodynamicpharmacogeneticpharmacokineticrivaroxaban

Identifiers

PMID42220444
PMCPMC13221595

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.