Evidence map›Paper›PMID 34149799›Full record

ArticleFrontiers in genetics2021

Interferon Lambda 3/4 (IFNλ3/4) rs12979860 Polymorphisms Is Not Associated With Susceptibility to Systemic Lupus Erythematosus, Although It Regulates OASL Expression in Patients With SLE.

Yaneli Juárez-Vicuña, Julia Pérez-Ramos, Laura Adalid-Peralta, Fausto Sánchez, Laura Aline Martínez-Martínez, María Del Carmen Ortiz-Segura, Edgar Pichardo-Ontiveros, Adrián Hernández-Díazcouder, Luis M Amezcua-Guerra, Julian Ramírez-Bello and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 11 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

11 authors at 6 institutions in 1 country.

Yaneli Juárez-VicuñaDepartment of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Julia Pérez-RamosDepartment of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico.
Laura Adalid-PeraltaUnit for the Study of Neuroinflammation in Neurological Pathologies, Instituto de Investigaciones Biomédicas, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.
Fausto SánchezDepartment of Agricultural and Animal Production, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico.
Laura Aline Martínez-MartínezDepartment of Rheumatology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
María Del Carmen Ortiz-SeguraLaboratory of Pharmacology and Toxicology, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
Edgar Pichardo-OntiverosDepartment of Nutrition Physiology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Adrián Hernández-DíazcouderDepartment of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Luis M Amezcua-GuerraDepartment of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Julian Ramírez-BelloUnit of Research, Hospital Juárez de México, Mexico City, Mexico.
Fausto Sánchez-MuñozDepartment of Immunology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Instituto Nacional de Cardiología · MXUniversidad Autónoma Metropolitana · MXHospital Infantil de México Federico Gómez · MXHospital Juárez de México · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXInstituto Nacional de Neurología y Neurocirugía · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease with a complex etiology. Various genetic factors are associated with susceptibility to developing SLE and contribute to its onset and progression. Different single-nucleotide polymorphisms (SNPs) have been associated with SLE in several populations. The rs12979860 SNP in interferon lambda 3/4 (IFNλ3/4) is significantly associated with SLE susceptibility in patients negative for nephritis in Taiwanese people, and interferon-stimulated genes (ISGs) are differentially expressed in normal liver by the rs12979860 genotype. This study aimed to investigate whether rs12979860 is associated with the presence of SLE and lupus nephritis in Mexican individuals as well as with the expression of several ISGs in SLE patients. In total, 439 SLE patients and 358 healthy donors were genotyped for rs12979860 using real-time PCR, and allelic discrimination plots were constructed. Additionally, peripheral blood mononuclear cells (PBMCs) were isolated from the venous blood of SLE patients by centrifugation (

Indexed as

interferons lambdainterferon-stimulated genesoligoadenylate sinthetase-likers12979860 SNPsystemic lupus erythematosus

Identifiers

PMID34149799
PMCPMC8206639
OpenAlexW3170565174

What OpenQuestion holds

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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 OpenQuestion graph.