Evidence map›Paper›PMID 35109858›Full record

ArticlePediatric rheumatology online journal2022

Prevalence of autoantibodies in patients with juvenile idiopathic arthritis: results from the German inception cohort ICON-JIA.

Caroline Schulz, Sabrina Fuehner, Bernhard Schlüter, Manfred Fobker, Claudia Sengler, Jens Klotsche, Martina Niewerth, Kirsten Minden, Dirk Foell

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Pediatric rheumatology online journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. Article
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 2 institutions in 1 country.

Caroline SchulzDepartment of Paediatric Rheumatology and Immunology, University Hospital Muenster, Albert-Schweitzer-Campus 1, Building D3, 48149, Muenster, Germany.
Sabrina FuehnerDepartment of Paediatric Rheumatology and Immunology, University Hospital Muenster, Albert-Schweitzer-Campus 1, Building D3, 48149, Muenster, Germany.
Bernhard SchlüterCentre of Laboratory Medicine, University Hospital Muenster, Muenster, Germany.
Manfred FobkerCentre of Laboratory Medicine, University Hospital Muenster, Muenster, Germany.
Claudia SenglerEpidemiology Unit, German Rheumatism Research Center, Berlin, Germany.
Jens KlotscheEpidemiology Unit, German Rheumatism Research Center, Berlin, Germany.
Martina NiewerthEpidemiology Unit, German Rheumatism Research Center, Berlin, Germany.
Kirsten MindenEpidemiology Unit, German Rheumatism Research Center, Berlin, Germany.
Dirk FoellDepartment of Paediatric Rheumatology and Immunology, University Hospital Muenster, Albert-Schweitzer-Campus 1, Building D3, 48149, Muenster, Germany. dfoell@uni-muenster.de.ORCID http://orcid.org/0000-0002-1946-3916
University Hospital Münster · DEGerman Rheumatism Research Centre · DE

Funding

BMBF 01ER0813BMBF FKZ 01ER0812
6 · The paper itself

Abstract

backgroundAn association of different autoimmune diseases is suspected. In juvenile idiopathic arthritis (JIA), only few and partially conflicting data on the co-existence of other autoimmune disorders are available. The prevalence of autoantibodies in patients with JIA in Germany is not known.

methodsSamples from 499 patients (median age at time of blood collection 11 years, median disease duration 4.4 years) in the prospective, multicenter inception cohort of children newly diagnosed with JIA (ICON-JIA) were analysed for the presence of anti-thyroid antibodies, celiac disease-specific antibodies (anti-tTG IgA, anti-tTG IgG), and connective tissue disease-associated antibodies (CTD-screen).

resultsA total of 76 (15.2%) patients had either clinically diagnosed autoimmune comorbidity or elevated autoantibodies. Of 21 patients with clinical autoimmune comorbidity, only 8 were also serologically positive at the time of testing, while 55 patients had autoantibodies without clinical diagnosis. Thus, 63 patients (12.6%) had at least one elevated autoantibody. Antibodies against thyroglobulin were found in 3% and against thyreoperoxidase in 4% of the samples. TSH receptor antibodies could not be detected in any of the 499 patients. Tissue transglutaminase antibodies were elevated in 0.4% of the patients. A positive screen for CTD-specific antinuclear antibodies was found in 7%, but only rarely specific antibodies (anti-dsDNA 1.4%, anti-SS-A and -SS-B 0.2% each, anti-CENP-B 0.4%) were confirmed.

conclusionsIn our study, a specific correlation between JIA and other autoimmune phenomena could not be confirmed. The lack of well-matched control groups makes interpretation challenging. Further data need to corroborate the suspected increased risk of developing other autoimmune phenomena in JIA patients.

Indexed as

AdolescentArthritis, JuvenileAutoantibodiesChildFemaleGermanyHumansLongitudinal StudiesMalePrevalenceProspective StudiesAutoantibodies

Identifiers

PMID35109858
PMCPMC8812016
OpenAlexW4210495260

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.