Evidence map›Paper›PMID 28619073›Full record

ArticleArthritis research & therapy2017

Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus.

Adrià Aterido, Antonio Julià, Patricia Carreira, Ricardo Blanco, José Javier López-Longo, José Javier Pérez Venegas, Àlex Olivé, José Luís Andreu, Maria Ángeles Aguirre-Zamorano, Paloma Vela and 15 more

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Oral Manifestations of Systemic Lupus Erythematosus: A Systematic Review.International journal of environmental research and public health · 2022
    Pooled it
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  4. 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

25 authors at 18 institutions in 2 countries.

Adrià AteridoRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Antonio JuliàRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain. toni.julia@vhir.org.ORCID 0000-0001-6064-3620
Patricia CarreiraRheumatology Department, Hospital Universitario 12 de Octubre, Madrid, 28041, Spain.
Ricardo BlancoRheumatology Department, Hospital Universitario Marqués de Valdecilla, Santander, 39008, Spain.
José Javier López-LongoRheumatology Department, Hospital Universitario Gregorio Marañón, Madrid, 28007, Spain.
José Javier Pérez VenegasRheumatology Department, Hospital del SAS de Jerez de la Frontera, Cádiz, 11407, Spain.
Àlex OlivéRheumatology Department, Hospital Universitari Germans Trias i Pujol, Badalona, 08916, Spain.
José Luís AndreuRheumatology Department, Hospital Universitario Puerta de Hierro, Madrid, 28222, Spain.
Maria Ángeles Aguirre-ZamoranoRheumatology Department, Hospital Universitario Reina Sofía, Córdoba, 14004, Spain.
Paloma VelaRheumatology Department, Hospital General Universitario de Alicante, Alicante, 03010, Spain.
Joan M NollaRheumatology Department, Hospital Universitari de Bellvitge, Barcelona, 08907, Spain.
José Luís Marenco-de la FuenteRheumatology Department, Hospital de Valme, Sevilla, 41014, Spain.
Antonio ZeaRheumatology Department, Hospital Universitario Ramón y Cajal, 28034, Madrid, Spain.
José María PegoInstituto de Investigación Biomédica de Vigo, Ourense y Pontevedra, 36204, Spain.
Mercedes FreireRheumatology Department, Hospital Universitario A Coruña, A Coruña, 15006, Spain.
Elvira DíezRheumatology Department, Hospital Complejo Asistencial Universitario de León, León, 24001, Spain.
María López-LasantaRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Mireia López-CorbetoRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Núria PalauRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Raül TortosaRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Josep Lluís GelpíLife Sciences, Barcelona Supercomputing Centre, Barcelona, 08034, Spain.
Devin AbsherHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, 35806, USA.
Richard M MyersHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, 35806, USA.
Antonio Fernández-NebroRheumatology Department, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain. afnebro@gmail.com.
Sara MarsalRheumatology Research Group, Vall d'Hebron Research Institute, Barcelona, 08035, Spain.
Vall d'Hebron Institut de Recerca · ESHudsonAlpha Institute for Biotechnology · USBarcelona Supercomputing Center · ESBellvitge University Hospital · ESComplexo Hospitalario Universitario A Coruña · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital General Universitario Gregorio Marañón · ESHospital Jerez Puerta del Sur · ESHospital Regional Universitario de Málaga · ESHospital Universitari Germans Trias i Pujol · ESHospital Universitario 12 De Octubre · ESHospital Universitario de Valme · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Ramón y Cajal · ESHospital Universitario Reina Sofía · ESMarqués de Valdecilla University Hospital · ESUniversidade de Vigo · ESUniversitat Pompeu Fabra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) is a genetically complex rheumatic disease characterized by heterogeneous clinical manifestations of unknown etiology. Recent studies have suggested the existence of a genetic basis for SLE heterogeneity. The objective of the present study was to identify new genetic variation associated with the clinically relevant phenotypes in SLE.

methodsA two-stage pathway-based approach was used to identify the genetic variation associated with the main clinical phenotypes in SLE. In the discovery stage, 482 SLE patients were genotyped using Illumina Human Quad610 microarrays. Association between 798 reference genetic pathways from the Molecular Signatures Database and 11 SLE phenotypes was tested using the set-based method implemented in PLINK software. Pathways significantly associated after multiple test correction were subsequently tested for replication in an independent cohort of 425 SLE patients. Using an in silico approach, we analyzed the functional effects of common SLE therapies on the replicated genetic pathways. The association of known SLE risk variants with the development of the clinical phenotypes was also analyzed.

resultsIn the discovery stage, we found a significant association between the vascular endothelial growth factor (VEGF) pathway and oral ulceration (P value for false discovery rate (P

conclusionsThe present study has identified VEGF genetic pathway association with the risk of oral ulceration in SLE. New therapies targeting the VEGF pathway could be more effective in reducing the severity of this phenotype. These findings represent a first step towards the understanding of the genetic basis of phenotype heterogeneity in SLE.

Indexed as

AdultFemaleGenetic Predisposition to DiseaseGenetic VariationGenome-Wide Association StudyGenotypeHumansLupus Erythematosus, SystemicMaleOral UlcerPhenotypeVascular Endothelial Growth Factor AVascular Endothelial Growth Factor AVEGFA protein, humanClinical phenotypesGeneticsGenome-wide pathway analysisOral ulcerationSystemic lupus erythematosus

Identifiers

PMID28619073
PMCPMC5471877
OpenAlexW2625903316

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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.