Evidence map›Paper›PMID 30225559›Full record

ArticleClinical rheumatology2019

Serum interleukin-37 level and interleukin-37 gene polymorphism in patients with Behçet disease.

Selcan Özgüçlü, Türker Duman, Funda Seher Özalp Ateş, Orhan Küçükşahin, Sevgi Çolak, Ümit Ölmez

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 15% 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, 21 citations in OpenAlex.

  1. Article
  2. Serum levels of IL-37 and correlation with inflammatory cytokines and clinical outcomes in patients with coronary artery disease.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2022
    Article
  3. Article
  4. Review
  5. Genetics in Behcet's Disease: An Update Review.Frontiers in ophthalmology · 2022
    Review
  6. A single nucleotide polymorphism in theInternational journal of ophthalmology · 2021
    Article
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Selcan ÖzgüçlüImmunology and Allergy, Ankara Dışkapı Yıldırım Beyazıt Education and Research Hospital, Ankara, Turkey. selcan.gultuna@gmail.com.
Türker DumanFaculty of Science, Biology, Ankara University, Ankara, Turkey.
Funda Seher Özalp AteşBiostatistics, Ankara University School of Medicine, Ankara, Turkey.
Orhan KüçükşahinRheumatology, Ankara Liv Hospital, Ankara, Turkey.
Sevgi ÇolakImmunology and Allergy, Ankara University School of Medicine, Ankara, Turkey.
Ümit ÖlmezImmunology and Allergy, Ankara University School of Medicine, Ankara, Turkey.
Ankara University · TRDışkapı Yıldırım Beyazıt Eğitim ve Araştırma Hastanesi · TRLiv Hospital · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behçet's disease (BD) is a chronic inflammatory disease. The etiopathogenesis of BD is not well understood and several cytokines and genetic factors have been investigated. Interleukin (IL)-37, which a member of IL-1 family is an anti-inflammatory cytokine. The aim of the study was to analyze serum IL-37 level and IL-37 gene polymorphisms to assess its possible role in BD. Two hundred twenty-three patients with BD and 80 healthy controls (HC) were enrolled. Serum IL-37 level was measured using an enzyme-linked immunosorbent assay (ELISA). Deoksiribo Nucleic acids (DNA) were extracted using a genomic DNA isolation kit. Single nucleotide polymorphism (SNP) of IL-37 gene (rs3811047) was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR/RFLP) methods. Serum IL-37 level was not significantly different in BD and HC (p > 0.05). Serum IL-37 level was not associated with the disease activity (p > 0.05). However, its level was higher in mucocutaneous involvement compared with systemic involvement (p = 0.002) and HC (p = 0.005). IL-37 gene polymorphisms were similar in BD and HC (p > 0.05). IL-37 may play a role in the etiopathogenesis of BD by contributing to manifestation with more moderate clinical symptoms.

Indexed as

AdultBehcet SyndromeCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansInterleukin-1Logistic ModelsMaleMiddle AgedPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideIL37 protein, humanInterleukin-1Behçet’s diseaseCytokineGene polymorphismInterleukin-37

Identifiers

PMID30225559
OpenAlexW2889708148

What OpenQuestion holds

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Read underepoch 390

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.