Evidence map›Paper›PMID 41977385›Full record

ArticleInternational journal of molecular sciences2026

Evaluation of +49 A>G (rs231775) Variant in CTLA4 Gene and SCTLA-4 Serum Levels in Plaque Psoriasis in a Mestizo Mexican Population.

María Guadalupe Cortés-Ruiz, Katia Alejandra Wheber-Hidalgo, Brenda Fernanda Hernández-Nicols, Fernando Gabriel Buenrostro-Camacho, Jorge Hernández-Bello, Omar Graciano-Machuca, Anabell Alvarado-Navarro

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

7 authors.

María Guadalupe Cortés-RuizCentro de Investigación en Inmunología y Dermatología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.
Katia Alejandra Wheber-HidalgoCentro de Investigación en Inmunología y Dermatología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.
Brenda Fernanda Hernández-NicolsCentro de Investigación en Inmunología y Dermatología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.ORCID 0009-0000-6469-3254
Fernando Gabriel Buenrostro-CamachoCentro de Investigación en Inmunología y Dermatología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.
Jorge Hernández-BelloInstituto de Investigación en Ciencias Biomédicas, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.ORCID 0000-0001-8004-1811
Omar Graciano-MachucaCentro de Investigación en Procesamiento Digital de Señales, Centro Universitario de los Valles, Universidad de Guadalajara, Carretera a Guadalajara, Supermanzana El Km 45.5, Caimanero 46708, Jalisco, Mexico.
Anabell Alvarado-NavarroCentro de Investigación en Inmunología y Dermatología, Departamento de Fisiología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Sierra Mojada 950, Colonia Independencia, Guadalajara 44340, Jalisco, Mexico.ORCID 0000-0002-5719-1712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plaque psoriasis (PP) is a chronic immune-mediated skin disorder characterized by T-cell dysregulation and an imbalance between regulatory T cells (Treg) and T helper 17 (Th17) cells. Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), a key inhibitory checkpoint molecule expressed on Treg cells, and its soluble isoform (sCTLA-4) are critical regulators of peripheral immune tolerance and may contribute to PP pathogenesis. This case-control study evaluated the association between the +49 A>G variant of the

Indexed as

CTLA-4 AntigenPolymorphism, Single NucleotidePsoriasisAdultAllelesCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansMaleMexicoMiddle AgedCTLA-4 AntigenCTLA4 protein, humanCTLA4 variantgenetic susceptibilityimmune checkpointplaque psoriasisrs231775soluble CTLA-4

Identifiers

PMID41977385
PMCPMC13073593

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Registered trials

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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.