Evidence map›Paper›PMID 37270806›Full record

ArticleBiomolecules & biomedicine2023

Analysis of GPR126 polymorphisms and their relationship with scoliosis in Marfan syndrome and Marfan-like syndrome in Mexican patients.

Maria Elena Soto, Giovanny Fuentevilla-Alvarez, Solange Gabriela Koretzky, Gilberto Vargas-Alarcón, Yazmín Estela Torres-Paz, Sergio Enrique Meza-Toledo, Israel Pérez-Torres, Claudia Huesca-Gómez, Ricardo Gamboa

Open access · diamondAbstract read
In one paragraph

Article in Biomolecules & biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Maria Elena SotoDepartment of Immunology, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México; Cardiovascular Line Department in American British Cowdray (ABC) Medical Center, México City, México.
Giovanny Fuentevilla-AlvarezDepartment of Physiology, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México; Department of Biochemistry, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (IPN), México City, México.
Solange Gabriela KoretzkyEditorial Department, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Gilberto Vargas-AlarcónResearch Direction, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Yazmín Estela Torres-PazDepartment of Physiology, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Sergio Enrique Meza-ToledoDepartment of Biochemistry, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional (IPN), México City, México.
Israel Pérez-TorresDepartment of Cardiovascular Biomedicine, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Claudia Huesca-GómezDepartment of Physiology, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Ricardo GamboaDepartment of Physiology, Instituto Nacional de Cardiología "Ignacio Chávez", México City, México.
Instituto Nacional de Cardiología · MXCentro Médico ABC · MXInstituto Nacional de Cardiologia · BRInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Marfan syndrome (MFS) is an inherited connective tissue disorder. As the spinal growth depends on delicate balance of forces, conditions that affect musculoskeletal matrix often lead to spinal deformities. A large cross-sectional study revealed a 63% prevalence of scoliosis among patients with MFS. Multi-ethnic genome-wide association studies and analyses of human genetic mutations showed that variations and mutations of G protein-coupled receptor 126 (GPR126)locus are associated with multiple skeletal defects, including shorter stature and adolescent idiopathic scoliosis. The study included 54 patients with MFS and 196 control patients. The DNA was extracted from peripheral blood using the saline expulsion method and single nucleotide polymorphism (SNP) determination was carried out using TaqMan probes. Allelic discrimination was performed by RT-qPCR. Significant differences in genotype frequencies were found for SNP rs6570507 in relation to MFS and sex (recessive model, OR 2.46, 95% CI 1.03 -5.87; P = 0.03) and rs7755109 (overdominant model, OR 0.39, 95% CI 0.16-0.91; P = 0.03). The most significant association was found in SNP rs7755109, where the frequency of genotype AG was significantly different between MFS patients with scoliosis and those without (OR 5.68, 95% CI 1.09-29.48; P=0.04). This study, for the first time, examined the genetic association of SNP GPR126 with the risk of scoliosis in patients with connective tissue diseases. The study revealed that SNP rs7755109 is associated with the presence of scoliosis in Mexican patients with MFS.

Indexed as

Marfan SyndromeScoliosisAdolescentCross-Sectional StudiesGenome-Wide Association StudyHumansReceptors, G-Protein-CoupledReceptors, G-Protein-Coupled

Identifiers

PMID37270806
PMCPMC10655884
OpenAlexW4379261079

What OpenQuestion holds

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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.