Evidence map›Paper›PMID 37798643›Full record

ArticlePediatric rheumatology online journal2023

Prevalence of tissue transglutaminase antibodies and IgA deficiency are not increased in juvenile idiopathic arthritis: a case-control study.

Angela Taneja Kohli, Aimee O Hersh, Lori Ponder, Lai Hin Kimi Chan, Kelly A Rouster-Stevens, Anne E Tebo, Subra Kugathasan, Stephen L Guthery, John F Bohnsack, Sampath Prahalad

Open access · goldAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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

10 authors at 3 institutions in 1 country.

Angela Taneja KohliDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA. Angela.Taneja@emory.edu.ORCID http://orcid.org/0000-0002-8104-873X
Aimee O HershDepartment of Pediatrics, Spencer F. Eccles School of Medicine, University of Utah, Salt Lake City, UT, USA.
Lori PonderChildren's Healthcare of Atlanta, Atlanta, GA, USA.
Lai Hin Kimi ChanDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Kelly A Rouster-StevensDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Anne E TeboUniversity of Utah, Salt Lake City, UT, USA.
Subra KugathasanDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Stephen L GutheryDepartment of Pediatrics, Spencer F. Eccles School of Medicine, University of Utah, Salt Lake City, UT, USA.
John F BohnsackDepartment of Pediatrics, Spencer F. Eccles School of Medicine, University of Utah, Salt Lake City, UT, USA.
Sampath PrahaladDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Emory University · USUniversity of Utah · USChildren's Healthcare of Atlanta · US

Funding

Marcus Foundation Marcus Foundation
6 · The paper itself

Abstract

backgroundThe prevalence of Celiac Disease (CD) in Juvenile Idiopathic Arthritis (JIA) has been reported to be 0.1-7% in various small studies. As a result of the limited number of research and their inconclusive results there are no clear recommendations for routine CD screening in asymptomatic patients with JIA. Our aim is to estimate the prevalence of IgA deficiency and tissue transglutaminase (tTG) IgA in a cohort of JIA followed in two large academic medical centers.

methodsSerum was collected and stored from all subjects and analyzed in a reference laboratory for total IgA (Quantitative Nephelometry) and tTG IgA antibody levels (Semi-Quantitative Enzyme-Linked Immunosorbent Assay). Fisher's exact tests were performed for statistical significance. Risk estimates (odds ratios) with 95% confidence intervals were calculated.

results808 JIA cases and 140 controls were analyzed. Majority were non-Hispanic whites (72% vs. 68% p = 0.309). A total of 1.2% of cases were IgA deficient compared to none of the controls (p = 0.373). After excluding IgA deficient subjects, 2% of cases had tTG IgA ≥ 4u/mL compared to 3.6% of controls (p = 0.216) (OR = 0.5; 95% C.I = 0.1-1.4); and 0.8% of cases had tTG IgA > 10u/mL compared to 1.4% of controls (p = 0.627) (OR = 0.5; 95%C.I = 0.1-2.9).

conclusionsUsing the largest JIA cohort to date to investigate prevalence of celiac antibodies, the prevalence of positive tTG IgA was 0.8% and of IgA deficiency was 1.2%. The results did not demonstrate a higher prevalence of abnormal tTG IgA in JIA. The study did not support the routine screening of asymptomatic JIA patients for CD.

Indexed as

Arthritis, JuvenileCeliac DiseaseIgA DeficiencyAutoantibodiesCase-Control StudiesHumansImmunoglobulin APrevalenceProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesAutoantibodiesImmunoglobulin AProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesCeliac antibodiesCeliac diseaseChildrenHealthy controlsIgA deficiencyJuvenile Idiopathic ArthritisPrevalenceTissue transglutaminase IgAtTG IgA

Identifiers

PMID37798643
PMCPMC10557180
OpenAlexW4387380768

What OpenQuestion holds

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LicenceCC BY
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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.