Evidence map›Paper›PMID 33259121›Full record

ArticlePediatric diabetes2021

Celiac disease can be predicted by high levels of tissue transglutaminase antibodies in children and adolescents with type 1 diabetes.

Mara Cerqueiro Bybrant, Elin Udén, Filippa Frederiksen, Anna L Gustafsson, Carl-Göran Arvidsson, Anna-Lena Fureman, Gun Forsander, Helena Elding Larsson, Sten A Ivarsson, Marie Lindgren and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Pediatric diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 11 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

19 authors at 10 institutions in 1 country.

Mara Cerqueiro BybrantPediatric Endocrinology Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-2560-0569
Elin UdénLund University, Lund, Sweden.
Filippa FrederiksenKarolinska Institutet, Stockholm, Sweden.
Anna L GustafssonChildren Clinic, Halland's Hospital, Halmstad, Sweden.
Carl-Göran ArvidssonDepartment of Pediatrics, Västmanland's Hospital, Västerås, Sweden.
Anna-Lena FuremanChildren's clinic, Östersund Hospital, Sweden.
Gun ForsanderDepartment of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-0266-9651
Helena Elding LarssonDepartment of Clinical Sciences, Lund University/Clinical Research Centre, Skåne University Hospital, Malmö, Sweden.ORCID 0000-0003-3306-1742
Sten A IvarssonDepartment of Clinical Sciences, Lund University, Skåne University Hospital, Pediatrics, Lund, Sweden.
Marie LindgrenDepartment of Clinical Sciences, Lund University, Skåne University Hospital, Pediatrics, Lund, Sweden.
Johnny LudvigssonCrown Princess Victoria's Children's and Youth Hospital, University Hospital, Linköping, Sweden.
Claude MarcusDivision of Pediatrics, Department of Clinical Science Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
Auste Pundziute LyckåDepartment of Pediatrics, Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden.
Martina PerssonDepartment of Medicine, Clinical Epidemiology, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-2268-3159
Ulf SamuelssonCrown Princess Victoria's Children's and Youth Hospital, University Hospital, Linköping, Sweden.ORCID 0000-0002-2837-4237
Stefan SärnbladSchool of Medical Sciences, Örebro University, Örebro, Sweden.ORCID 0000-0002-1440-9961
Karin ÅkessonDepartment of Pediatrics, Ryhov County Hospital, Jönköping, Sweden.
Eva ÖrtqvistPediatric Endocrinology Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-6924-704X
Annelie CarlssonDepartment of Clinical Sciences, Lund University, Skåne University Hospital, Pediatrics, Lund, Sweden.ORCID 0000-0003-2361-7743
Lund University · SEKarolinska Institutet · SELinköping University · SESahlgrenska University Hospital · SEHallands sjukhus Halmstad · SEKarolinska University Hospital · SEÖrebro University · SEÖstersunds Hospital · SERyhov Hospital Jönköping · SEVästmanlands sjukhus Västerås · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesChildren with type 1 diabetes (T1D) are not included in guidelines regarding diagnosis criteria for celiac disease (CD) without a diagnostic biopsy, due to lack of data. We explored whether tissue transglutaminase antibodies (anti-tTG) that were ≥ 10 times the upper limit of normal (10× ULN) predicted CD in T1D.

methodsData from the Swedish prospective Better Diabetes Diagnosis study was used, and 2035 children and adolescents with T1D diagnosed between 2005-2010 were included. Of these, 32 had been diagnosed with CD before T1D. The children without CD were repeatedly screened for CD using anti-tTG antibodies of immunoglobulin type A. In addition, their human leukocyte antigen (HLA) were genotyped. All children with positive anti-tTG were advised to undergo biopsy. Biopsies were performed on 119 children and graded using the Marsh-Oberhüber classification.

resultsAll of the 60 children with anti-tTG ≥10x ULN had CD verified by biopsies. The degree of mucosal damage correlated with anti-tTG levels. Among 2003 screened children, 6.9% had positive anti-tTG and 5.6% were confirmed CD. The overall CD prevalence, when including the 32 children with CD before T1D, was 7.0% (145/2035). All but one of the children diagnosed with CD had HLA-DQ2 and/or DQ8.

conclusionsAs all screened children and adolescents with T1D with tissue transglutaminase antibodies above 10 times the positive value 10x ULN had CD, we propose that the guidelines for diagnosing CD in screened children, when biopsies can be omitted, should also apply to children and adolescents with T1D as a noninvasive method.

Indexed as

AdolescentAge FactorsAutoantibodiesCeliac DiseaseChildChild, PreschoolCohort StudiesDiabetes Mellitus, Type 1FemaleHumansMalePredictive Value of TestsSwedenTransglutaminasesanti-transglutaminase autoantibodyAutoantibodiesTransglutaminasesbiopsyceliac diseasescreeningtissue transglutaminase antibodiestype 1 diabetes

Identifiers

PMID33259121
PMCPMC8048786
OpenAlexW3109620861

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LicenceCC BY-NC-ND
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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.