Evidence map›Paper›PMID 35207358›Full record

ReviewJournal of clinical medicine2022

Celiac Disease in Juvenile Idiopathic Arthritis and Other Pediatric Rheumatic Disorders.

Dimitri Poddighe, Micol Romano, Kuanysh Dossybayeva, Diyora Abdukhakimova, Dinara Galiyeva, Erkan Demirkaya

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Review
  6. Article
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  10. Observational
  11. Article
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  13. Article
  14. Screening for celiac disease in juvenile idiopathic arthritis.Pediatric rheumatology online journal · 2022
    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

6 authors at 3 institutions in 2 countries.

Dimitri PoddigheDepartment of Medicine, Nazarbayev University School of Medicine (NUSOM), Nur-Sultan 010000, Kazakhstan.ORCID 0000-0001-6431-9334
Micol RomanoDivision of Pediatric Rheumatology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.
Kuanysh DossybayevaDepartment of Medicine, Nazarbayev University School of Medicine (NUSOM), Nur-Sultan 010000, Kazakhstan.ORCID 0000-0002-1834-1909
Diyora AbdukhakimovaDepartment of Medicine, Nazarbayev University School of Medicine (NUSOM), Nur-Sultan 010000, Kazakhstan.
Dinara GaliyevaDepartment of Medicine, Nazarbayev University School of Medicine (NUSOM), Nur-Sultan 010000, Kazakhstan.
Erkan DemirkayaDivision of Pediatric Rheumatology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.ORCID 0000-0003-4525-1789
Nazarbayev University · KZWestern University · CANational Research Center for Maternal and Child Health · KZ

Funding

Nazarbayev University 240919FD3912
6 · The paper itself

Abstract

Celiac Disease (CD) is an immune-mediated and gluten-related disorder whose prevalence is higher in children affected with other autoimmune disorders, including diabetes mellitus type 1, autoimmune thyroiditis, and others. As regards Juvenile Idiopathic Arthritis (JIA) and other pediatric rheumatic disorders, there is no clear recommendation for CD serological screening. In this review, we analyze all the available clinical studies investigating CD among children with JIA (and other rheumatic diseases), in order to provide objective data to better understand the necessity of CD serological screening during the follow-up. Based on the present literature review and analysis, >2.5% patients with JIA were diagnosed with CD; however, the CD prevalence in JIA patients may be even higher (>3-3.5%) due to several study limitations that could have underestimated CD diagnosis to a variable extent. Therefore, serological screening for CD in children affected with JIA could be recommended due to the increased CD prevalence in these patients (compared to the general pediatric population), and because these JIA patients diagnosed with CD were mostly asymptomatic. However, further research is needed to establish a cost-effective approach in terms of CD screening frequency and modalities during the follow-up for JIA patients. Conversely, at the moment, there is no evidence supporting a periodical CD screening in children affected with other rheumatic diseases (including pediatric systemic lupus erythematosus, juvenile dermatomyositis, and systemic sclerosis).

Indexed as

celiac diseasejuvenile dermatomyositisjuvenile idiopathic arthritispediatric systemic lupus erythematosusprevalencescreeningsystemic scleroderma

Identifiers

PMID35207358
PMCPMC8878661
OpenAlexW4214764584

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.