Evidence map›Paper›PMID 32809147›Full record

SynthesisClinical rheumatology2021

TNFSF4 is a risk factor to systemic lupus erythematosus in a Latin American population.

Mario Adán Moreno-Eutimio, Carmen Estefanía Martínez-Alemán, Ivan Sammir Aranda-Uribe, Guillermo Aquino-Jarquin, Carlos Cabello-Gutierrez, José Manuel Fragoso, Rosa Elda Barbosa-Cobos, Miguel A Saavedra, Julian Ramírez-Bello

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Clinical rheumatology, 2021. 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
0.9field-weighted citation impact, top 25% 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. Article
  2. 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

9 authors at 6 institutions in 1 country.

Mario Adán Moreno-EutimioFacultad de Química, Universidad Nacional Autónoma de México (UNAM), Ciudad de México, México.
Carmen Estefanía Martínez-AlemánUnidad de Investigación, Hospital Juárez de México, Mexico City, Mexico.
Ivan Sammir Aranda-UribeUnidad de Investigación, Hospital Juárez de México, Mexico City, Mexico.
Guillermo Aquino-JarquinLaboratorio de Investigación en Genómica, Genética y Bioinformática, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Carlos Cabello-GutierrezDepartamento de Investigación en Virología y Micología, Instituto Nacional de Enfermedades Respiratorias, Mexico City, Mexico.
José Manuel FragosoDepartamento de Biología Molecular, Instituto Nacional de Cardiología, Mexico City, Mexico.
Rosa Elda Barbosa-CobosServicio de Reumatología, Hospital Juárez de México, Mexico City, Mexico.
Miguel A SaavedraCentro Médico Nacional "La Raza", IMSS, Mexico City, Mexico.
Julian Ramírez-BelloUnidad de Investigación, Hospital Juárez de México, Mexico City, Mexico. dr.julian.ramirez.hjm@gmail.com.ORCID http://orcid.org/0000-0002-4153-9315
Hospital Juárez de México · MXCentro Médico Nacional La Raza · MXHospital Infantil de México Federico Gómez · MXInstituto Nacional de Cardiología · MXInstituto Nacional de Enfermedades Respiratorias · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to examine the association of three TNFSF4 single nucleotide variants (SNVs) with systemic lupus erythematosus (SLE) susceptibility in Mexican patients.

methodsGenotypes of the TNFSF4 rs1234315T/C, rs2205960G/T, and rs704840T/G SNVs were determined using a TaqMan assay. In our study, we included 395 patients with SLE and 500 controls.

resultsOur information shows a significant difference in the allelic and genotypic frequency of the three TNFSF4 SNVs between cases and controls. Thus, our data showed an association between TNFSF4 rs1234315T/C (T vs. C, OR 1.40, p = 0.00087), rs2205960G/T (G vs. T, OR 1.32, p = 0.0037), and rs704840T/G (T vs. G, OR 1.41, p = 0.0003) and SLE susceptibility in Mexican subjects. Besides, we conducted a meta-analysis to determine the role of TNFSF4 rs2205960G/T and SLE susceptibility; our results showed that this variant is a risk factor for SLE in Latin Americans and Asians.

conclusionOur results show that TNFSF4 rs1234315T/C, rs2205960G/T, and rs704840T/G are risk factors to SLE in Mexicans. This is the first study to document an association between TNFSF4 rs704840T/G and SLE in a Latin American population. In addition, our meta-analysis showed that TNFSF4 rs2205960G/T is a risk factor for Asians and Latin Americans. Key Point • The TNFSF4 rs1234315T/C, rs2205960G/T, and rs704849T/G SNVs are risk factors to SLE in patients from Mexico.

Indexed as

Genetic Predisposition to DiseaseLupus Erythematosus, SystemicGenotypeHumansLatin AmericaMexicoOX40 LigandPolymorphism, Single NucleotideRisk FactorsOX40 LigandTNFSF4 protein, humanSingle nucleotide variants susceptibilitySystemic lupus erythematosusTumor necrosis factor ligand superfamily member 4

Identifiers

PMID32809147
OpenAlexW3060766575

What Socratic holds

Textmetadata
Read underepoch 390

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.