Evidence map›Paper›PMID 30171379›Full record

ArticleClinical rheumatology2018

Evaluation of plasma microRNA expressions in patients with juvenile idiopathic arthritis.

Ferhat Demir, Alper Han Çebi, Mukaddes Kalyoncu

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 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

3 authors at 1 institution in 1 country.

Ferhat DemirDepartment of Pediatric Rheumatology, Faculty of Medicine, Karadeniz Technical University, 61187, Trabzon, Turkey. drferhat@outlook.com.ORCID http://orcid.org/0000-0001-9801-925X
Alper Han ÇebiDepartment of Medical Genetics, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Mukaddes KalyoncuDepartment of Pediatric Rheumatology, Faculty of Medicine, Karadeniz Technical University, 61187, Trabzon, Turkey.
Karadeniz Technical University · TR

Funding

Karadeniz Teknik Üniversitesi (TR) THD-16-5492
6 · The paper itself

Abstract

Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease of childhood, yet its etiology is unknown. It is known that microribonucleic acids (miRNAs) play a role in immunoregulation. We aimed to evaluate the plasma expression of some candidate miRNAs that are associated with the pathogenesis of autoimmunity. Thirty-one patients diagnosed with JIA and age-sex-matched 31 healthy children were enrolled for the study. The plasma levels of four candidate miRNAs (miRNA-16, miRNA-155, miRNA-204, and miRNA-451), which are known to be associated with autoimmunity, were examined in all the subjects. The plasma levels of miRNAs were measured with real-time PCR in the patients in active and inactive periods and in the healthy controls. The groups were compared with each other. The plasma miRNA-155 levels were found to increase in the JIA patients compared to the healthy controls, and it was statistically more significant in the inactive period. We found that the JIA patients had the higher levels of miRNA-16 and the lower levels of miRNA-204/miRNA-451 expressions compare with the control group, but there was no statistically significant difference. A statistically significant decrease in the plasma levels of miRNA-204 was found in the patients that were in inactive disease with only methotrexate therapy. The plasma miRNA expressions were compared in the JIA subtypes, and it was observed that miRNA-204 levels were higher in polyarticular JIA and miRNA-451 levels were higher in enthesitis-related arthritis without statistical significance. The significant alterations in the plasma expression of miRNA-155 and miRNA-204 suggest to us that these molecules may be related to the pathogenesis of JIA. More comprehensive and functional researches about the role of these molecules are needed in this regard.

Indexed as

AutoimmunityAdolescentApoptosisArthritis, JuvenileCase-Control StudiesChildFemaleHumansMaleMicroRNAsMicroRNAsMIRN155 microRNA, humanMIRN16 microRNA, humanMIRN204 microRNA, humanMIRN451 microRNA, humanJuvenile idiopathic arthritisMicroRNAsMiRNA-155MiRNA-16MiRNA-204MiRNA-451

Identifiers

PMID30171379
OpenAlexW2888792319

What OpenQuestion holds

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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.