Evidence map›Paper›PMID 37289314›Full record

ArticleClinical rheumatology2023

The association between CYB5A gene rs1790834 polymorphism and clinical improvement after 6 months of leflunomide treatment in women with rheumatoid arthritis.

Filip Machaj, Jakub Rosik, Bartosz Szostak, Damian Malinowski, Krzysztof Safranow, Gabriela Olędzka, Emilia Wiechec, Andrzej Pawlik

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Article in Clinical rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 42% of its field
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 citations in OpenAlex.

  1. Review
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

8 authors at 3 institutions in 2 countries.

Filip MachajDepartment of Physiology, Pomeranian Medical University, 70-111, Szczecin, Poland.
Jakub RosikDepartment of Physiology, Pomeranian Medical University, 70-111, Szczecin, Poland.
Bartosz SzostakDepartment of Physiology, Pomeranian Medical University, 70-111, Szczecin, Poland.
Damian MalinowskiDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University, 70-111, Szczecin, Poland.
Krzysztof SafranowDepartment of Biochemistry and Medical Chemistry, Pomeranian Medical University, 70-111, Szczecin, Poland.
Gabriela OlędzkaDepartment of Medical Biology, Medical University of Warsaw, 00-575, Warsaw, Poland.
Emilia WiechecDivision of Cell Biology, Department of Biomedical and Clinical Sciences, Linköping University, 581 85, Linköping, Sweden.
Andrzej PawlikDepartment of Physiology, Pomeranian Medical University, 70-111, Szczecin, Poland. pawand@poczta.onet.pl.ORCID http://orcid.org/0000-0001-6557-1208
Pomeranian Medical University · PLMedical University of Warsaw · PLLinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectivesRheumatoid arthritis (RA) is a disease affecting around 1% of the population in developed countries and can be treated with leflunomide. The higher prevalence of RA among women and numerous previous studies suggested the crucial role of sex hormones. Cytochrome CYB5A regulates the synthesis of androgens. Therefore, the aim of this study was to determine the association between common CYB5A gene polymorphism and the response to leflunomide in women with RA.

methodsThis study included 111 patients. All of them received oral leflunomide monotherapy at a dose of 20 mg daily. Women were genotyped for the presence of CYB5A rs1790834 polymorphism and evaluated monthly for 6 months following the initiation of treatment.

resultsAfter 6 months of therapy, patients with the GG genotype had higher DAS28 values and less improvement in DAS28 compared to patients with the GA and AA genotypes (p = 0.04). No statistically significant differences were found in relation to other disease activity parameters.

conclusionsThe results of the current study suggest a possible association of the CYB5A rs1790834 polymorphism with some disease activity parameters in RA patients treated with leflunomide during the initial therapy period. However, confirmation of the effect of this polymorphism on the efficacy of leflunomide treatment requires further studies. Key Points • Leflunomide is the synthetic disease-modifying anti-rheumatic drug used in the therapy of rheumatoid arthritis. • CYB5A rs1790834 gene polymorphism may influence the clinical improvement after 6 months of leflunomide treatment in women with rheumatoid arthritis.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidCytochromes b5FemaleHumansIsoxazolesLeflunomidePolymorphism, GeneticTreatment OutcomeAntirheumatic AgentsCYB5A protein, humanCytochromes b5IsoxazolesLeflunomideLeflunomidePolymorphismRheumatoid arthritisTherapy

Identifiers

PMID37289314
OpenAlexW4379768682

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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.