Evidence map›Paper›PMID 30559453›Full record

ArticleScientific reports2018

Extracellular vesicles are associated with the systemic inflammation of patients with seropositive rheumatoid arthritis.

Catalina Burbano, Mauricio Rojas, Carlos Muñoz-Vahos, Adriana Vanegas-García, Luis A Correa, Gloria Vásquez, Diana Castaño

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 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

7 authors at 2 institutions in 1 country.

Catalina BurbanoGrupo de Inmunología Celular e Inmunogenética, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia UdeA, Calle 70 No 52-21, Medellín, Colombia.
Mauricio RojasGrupo de Inmunología Celular e Inmunogenética, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia UdeA, Calle 70 No 52-21, Medellín, Colombia.
Carlos Muñoz-VahosSección de Reumatología, Hospital Universitario de San Vicente Fundación, Medellín, Colombia.
Adriana Vanegas-GarcíaSección de Reumatología, Hospital Universitario de San Vicente Fundación, Medellín, Colombia.ORCID http://orcid.org/0000-0003-0916-7715
Luis A CorreaSección de Dermatología, Departamento de Medicina Interna, Facultad de Medicina, Universidad de Antioquia, Laboratorio Clínico VID, Obra de la Congregación Mariana, Medellín, Colombia.
Gloria VásquezGrupo de Inmunología Celular e Inmunogenética, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia UdeA, Calle 70 No 52-21, Medellín, Colombia.
Diana CastañoGrupo de Inmunología Celular e Inmunogenética, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia UdeA, Calle 70 No 52-21, Medellín, Colombia. diana.castano@udea.edu.co.
Universidad de Antioquia · COHospital Universitario de San Vicente Fundación · CO

Funding

Universidad de Antioquia (University of Antioquia) Sostenibilidad and Sistema Universitario de Investigaciones, CODI (2013-05-42869836)
6 · The paper itself

Abstract

Patients with rheumatoid arthritis (RA) and autoantibodies, such as rheumatoid factor and those against cyclic citrullinated peptides, are designated as seropositive and have a more severe disease with worse prognosis than seronegative RA patients. Understanding the factors that participate in systemic inflammation, in addition to articular commitment, would allow better treatment approaches for prevention of RA comorbidities and disease reactivation. We evaluated whether monocyte subsets and extracellular vesicles (EVs) could contribute to this phenomenon. Seropositive patients had higher levels of proinflammatory cytokines than those of seronegative patients and healthy controls (HCs); however, this systemic inflammatory profile was unrelated to disease activity. High frequencies of circulating EVs positive for IgG, IgM, CD41a, and citrulline, together with altered counts and receptor expression of intermediate monocytes, were associated with systemic inflammation in seropositive patients; these alterations were not observed in seronegative patients, which seem to be more similar to HCs. Additionally, the EVs from seropositive patients were able to activate mononuclear phagocytes in vitro, and induced proinflammatory cytokines that were comparable to the inflammatory response observed at the systemic level in seropositive RA patients; therefore, all of these factors may contribute to the greater disease severity that has been described in these patients.

Indexed as

AdultAgedArthritis, RheumatoidAutoantibodiesCase-Control StudiesCytokinesExtracellular VesiclesFemaleHumansInflammationMaleMiddle AgedMonocytesPeptides, CyclicRheumatoid FactorAutoantibodiescyclic citrullinated peptideCytokinesPeptides, CyclicRheumatoid Factor

Identifiers

PMID30559453
PMCPMC6297132
OpenAlexW2904339539

What Socratic 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 Socratic graph.