Evidence map›Paper›PMID 31820195›Full record

ReviewInflammopharmacology2020

Influence of treatments on cell adhesion molecules in patients with systemic lupus erythematosus and rheumatoid arthritis: a review.

Lorena Flor da Rosa Franchi Santos, Neide Tomimura Costa, Michael Maes, Andréa Name Colado Simão, Isaias Dichi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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  10. Altered protein secretion in Batten disease.Disease models & mechanisms · 2021
    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

5 authors at 2 institutions in 2 countries.

Lorena Flor da Rosa Franchi SantosLaboratory of Research in Applied Immunology, University of Londrina, Londrina, PR, Brazil.
Neide Tomimura CostaDepartment of Rheumatology, University of Londrina, Londrina, PR, Brazil.
Michael MaesIMPACT Strategic Research Centre, School of Medicine, Deakin University, Geelong, VIC, Australia.
Andréa Name Colado SimãoDepartment of Pathology and Clinical Analysis and Toxicology, Laboratory of Research in Applied Immunology, University of Londrina, Rua Robert Koch, n 60., Londrina, PR, Brazil. deianame@yahoo.com.br.ORCID http://orcid.org/0000-0002-2073-6782
Isaias DichiDepartment of Internal Medicine and Laboratory of Research in Applied Immunology, University of Londrina, Londrina, PR, CEP 86038-440, Brazil.
Universidade Estadual de Londrina · BRDeakin University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are autoimmune diseases characterized by changes in cell adhesion molecules (CAMs).

objectiveTo review the influence of the main drugs used in the treatment of SLE and RA on CAM levels.

methodsA bibliographic search was performed using electronic databases. The research included human studies, in vivo or in vitro, with an experimental or observational design, and with no limit of publication date or number of subjects. Animal studies and non-standard treatments were not considered.

resultsWe included 21 studies, 3 on SLE and 18 on RA with monotherapy or combined trials. The most used drugs were cyclophosphamide (CY, in 2 studies) and methylprednisolone pulse (pMP, n = 2) in SLE; and methotrexate (MTX, n = 9) and infliximab (IFX, n = 4) in RA. In addition, the most frequently examined CAMs to predict response to treatment were vascular cell adhesion molecule-1 (VCAM-1, n = 2) in SLE, and intercellular adhesion molecule-1 (ICAM-1, n = 12), VCAM-1 (n = 12), and E-selectin (n = 14) in RA. After treatment, CAM levels were decreased in SLE and RA patients with active disease.

conclusionsIt is concluded that the CAM biomarkers may reflect disease activity and the response to treatment in SLE and RA patients.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidCell Adhesion MoleculesHumansImmunosuppressive AgentsLupus Erythematosus, SystemicTreatment OutcomeAntirheumatic AgentsCell Adhesion MoleculesImmunosuppressive AgentsAntirheumatic drugsCell adhesion moleculesRheumatoid arthritisSystemic lupus erythematosus

Identifiers

PMID31820195
OpenAlexW2993007441

What OpenQuestion 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 OpenQuestion graph.