Evidence map›Paper›PMID 36551311›Full record

ArticleBiomolecules2022

Vascular Endothelial Growth Factor and Its Soluble Receptor in Systemic Lupus Erythematosus Patients.

Fuensanta Gómez-Bernal, Yolanda Fernández-Cladera, Juan Carlos Quevedo-Abeledo, María García-González, Agustín F González-Rivero, Antonia de Vera-González, Candelaria Martín-González, Miguel Á González-Gay, Iván Ferraz-Amaro

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
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  5. 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 4 institutions in 2 countries.

Fuensanta Gómez-BernalDivision of Central Laboratory, Hospital Universitario de Canarias, 38320 Tenerife, Spain.
Yolanda Fernández-CladeraDivision of Central Laboratory, Hospital Universitario de Canarias, 38320 Tenerife, Spain.
Juan Carlos Quevedo-AbeledoDivision of Rheumatology, Hospital Doctor Negrín, 35010 Las Palmas de Gran Canaria, Spain.ORCID 0000-0003-0398-9072
María García-GonzálezDivision of Rheumatology, Hospital Universitario de Canarias, 38320 Tenerife, Spain.
Agustín F González-RiveroDivision of Central Laboratory, Hospital Universitario de Canarias, 38320 Tenerife, Spain.ORCID 0000-0002-9712-6990
Antonia de Vera-GonzálezDivision of Central Laboratory, Hospital Universitario de Canarias, 38320 Tenerife, Spain.
Candelaria Martín-GonzálezDivision of Internal Medicine, Hospital Universitario de Canarias, 38320 Tenerife, Spain.ORCID 0000-0002-4702-1840
Miguel Á González-GayEpidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Hospital Universitario Marqués de Valdecilla, IDIVAL, 39011 Santander, Spain.ORCID 0000-0002-7924-7406
Iván Ferraz-AmaroDivision of Rheumatology, Hospital Universitario de Canarias, 38320 Tenerife, Spain.ORCID 0000-0003-0197-5267
Hospital Universitario de Canarias · ESUniversidad de La Laguna · ESHospital Universitario de Gran Canaria Doctor Negrín · ESUniversidad de Cantabria · ES

Funding

Instituto de Salud Carlos III PI20/00084
6 · The paper itself

Abstract

Vascular endothelial growth factor (VEGF) is a major regulator of physiological and pathological angiogenesis. Its soluble receptor (sVEGFR) is a potent VEGF antagonist. Systemic lupus erythematosus (SLE) is an autoimmune disease with a diverse array of clinical manifestations that affect virtually any organ. We aimed to analyze the relationship of VEGF and sVEGFR with SLE disease-related features including disease activity, damage, and severity. Serum levels of VEGF165 isoform and sVEGFR (receptor 1) were assessed in 284 well-characterized patients with SLE. Linear regression analysis was performed to analyze the relationship of disease characteristics with both VEGF and sVEGFR. Patients with a disease damage index (SLICC score) equal to or greater than 1 had significantly elevated serum levels of VEGF and sVEGFR. Regarding disease-specific features, musculoskeletal manifestations were the disease feature most commonly associated with the upregulation of both VEGF and sVEGFR. SLE disease damage is associated with higher levels of VEGF and sVEGFR.

Indexed as

Lupus Erythematosus, SystemicVascular Endothelial Growth Factor AHumansNeovascularization, PathologicVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Vascular Endothelial Growth Factor Receptor-2systemic lupus erythematosusvascular endothelial growth factor

Identifiers

PMID36551311
PMCPMC9775345
OpenAlexW4313237602

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.