Evidence map›Paper›PMID 30758239›Full record

ArticleGenetic testing and molecular biomarkers2019

miRNA-24 Gene Sequence, DHFR -829C-T Genotypes, and Methotrexate Response in Mexican Patients with Rheumatoid Arthritis.

Martha Rocio Hernández-Preciado, María Cristina Morán-Moguel, Ingrid Patricia Dávalos-Rodríguez, Christian Michel Enríquez-Barajas, Juan Paulo Valdovinos-Maravilla, Ana Lilia Díaz-Pérez, Daniel Efraín Silva-Castro, Laura González-López, Jorge Ivan Gámez-Nava, Mario Alberto Aceves-Aceves and 1 more

Open access · hybridAbstract read
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Article in Genetic testing and molecular biomarkers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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 at 6 institutions in 2 countries.

Martha Rocio Hernández-Preciado1 Doctorado en Farmacología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.
María Cristina Morán-Moguel2 Departamento de DFMI, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.
Ingrid Patricia Dávalos-Rodríguez3 División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco México.
Christian Michel Enríquez-Barajas5 Servicio Social en Investigación. Comisión Interinstitucional para la Formación de Recursos Humanos para la Salud, Secretaría de Salud, México.
Juan Paulo Valdovinos-Maravilla5 Servicio Social en Investigación. Comisión Interinstitucional para la Formación de Recursos Humanos para la Salud, Secretaría de Salud, México.
Ana Lilia Díaz-Pérez5 Servicio Social en Investigación. Comisión Interinstitucional para la Formación de Recursos Humanos para la Salud, Secretaría de Salud, México.
Daniel Efraín Silva-Castro5 Servicio Social en Investigación. Comisión Interinstitucional para la Formación de Recursos Humanos para la Salud, Secretaría de Salud, México.
Laura González-López1 Doctorado en Farmacología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.
Jorge Ivan Gámez-Nava1 Doctorado en Farmacología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.
Mario Alberto Aceves-Aceves8 División de Investigación en Salud, Unidad Médica de Alta Especialidad, Hospital de Especialidades, Centro Médico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.
Mario Salazar-Páramo1 Doctorado en Farmacología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.
Universidad de Guadalajara · MXSecretaria de Salud · MXHospital de Especialidades · MXHospital General De Zona · MXMexican Social Security Institute · MXSecretaria de Salud · HN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe present study looked for variation in the miRNA-24 sequence, and evaluated the associations between the dihydrofolate reductase (DHFR) gene-829 C-T polymorphism and plasma DHFR concentrations with response to methotrexate (MTX) treatment in Mexican patients with rheumatoid arthritis (RA).

methodsA total of 135 women with RA were classified as responders (disease activity score [DAS28] <3.2) or nonresponders to MTX (DAS28 > 3.2). We determined the genotype of the patients using the polymerase chain reaction-restriction fragment length polymorphism method. Plasma DHFR enzyme levels and mi-RNA24 sequences were assessed by enzyme-linked immunosorbent assay (ELISA) and Sanger sequencing, respectively. Allelic frequencies and the genotypic distribution of the polymorphism were analyzed by the chi-square test.

resultsThe genotype frequencies of the DHFR -829C-T polymorphism among responders were 37.0% CC, 52.1% CT, and 10.9% TT and for nonresponders were 33.9% CC, 56.4% CT, and 9.7% TT. No significant differences in genotype frequencies were found between the groups (p = 0.88). The DHFR levels relative to genotype for responders were 6.8 ± 2.7, 6.1 ± 2.7, and 6.5 ± 1.5 ng/mL for CC, CT, and TT, respectively, and for nonresponders were 6.5 ± 2.0, 6.1 ± 3.1, and 7.4 ± 1.8 ng/mL for CC, CT, and TT, respectively. No significant differences were found between the two groups. Similarly, both groups showed no sequence variations in miRNA-24 gene.

conclusionThe -829C-T polymorphism of DHFR gene was not associated with response to MTX by RA patients, and no variations were found in the miRNA-24 sequence that might modify the response to treatment or DHFR enzyme levels in a Mexican population with RA.

Indexed as

AdultAgedAllelesArthritis, RheumatoidBiomarkers, PharmacologicalFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansMethotrexateMexicoMicroRNAsMiddle AgedPolymorphism, Single NucleotideTetrahydrofolate DehydrogenaseBiomarkers, PharmacologicalMethotrexateMicroRNAsMIRN24 microRNA, humanTetrahydrofolate Dehydrogenasegenotypemethotrexaterheumatoid arthritis

Identifiers

PMID30758239
PMCPMC6450450
OpenAlexW2911555394

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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.