Evidence map›Paper›PMID 34921003›Full record

ArticleArchives of disease in childhood2022

Five-year follow-up of new cases after a coeliac disease mass screening.

Olof Sandström, Fredrik Norström, Annelie Carlsson, Lotta Högberg, Maria van der Palz, Lars Stenhammar, Charlotta Webb, Anneli Ivarsson, Anna Myléus

Open access · hybridAbstract read
In one paragraph

Article in Archives of disease in childhood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Population level screening for celiac disease: is now the time?Current opinion in gastroenterology · 2023
    Review
  3. Article
  4. 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 3 institutions in 1 country.

Olof SandströmDepartment of Clinical Sciences, Paediatrics, Umea University, Umea, Sweden olof.sandstrom@umu.se.ORCID 0000-0003-0899-0531
Fredrik NorströmDepartment of Epidemiology and Global Health, Umea University, Umea, Sweden.
Annelie CarlssonDepartment of Clinical Sciences, Paediatrics, Lund University, Lund, Sweden.
Lotta Högberg4Department of Clinical and Experimental Medicine, Paediatrics, Linköping University, Linkoping, Östergötland, Sweden.
Maria van der PalzDepartment of Clinical Sciences, Paediatrics, Lund University, Lund, Sweden.
Lars Stenhammar4Department of Clinical and Experimental Medicine, Paediatrics, Linköping University, Linkoping, Östergötland, Sweden.
Charlotta WebbDepartment of Clinical Sciences, Paediatrics, Lund University, Lund, Sweden.
Anneli IvarssonDepartment of Epidemiology and Global Health, Umea University, Umea, Sweden.
Anna MyléusDepartment of Public Health and Clinical Medicine, Family Medicine, Umea University, Umea, Sweden.ORCID 0000-0003-2478-9598
Umeå University · SELund University · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe previously performed a population-based mass screening of coeliac disease in children aged 12 years in two birth cohorts resulting in 296 seropositive children, of whom 242 were diagnosed with coeliac disease after duodenal biopsies. In this follow-up study, we wanted to identify new cases in the screening population that tested negative-either converting from potential coeliac disease (seropositive but normal duodenal mucosa) or converting from seronegative at screening to diagnosed coeliac disease.

methodsAll seropositive children were invited to a follow-up appointment 5 years after the screening with renewed serological testing and recommended endoscopic investigation if seropositive. Seronegative children in the screening study (n=12 353) were linked to the National Swedish Childhood Coeliac Disease Register to find cases diagnosed in healthcare during the same period.

resultsIn total, 230 (77%) came to the follow-up appointment, including 34 of 39 with potential coeliac disease. Of these, 11 (32%) had converted to coeliac disease. One new case was found in the National Swedish Childhood Coeliac Disease Register who received the diagnosis through routine screening in children with type 1 diabetes.

conclusionsThere is a high risk of conversion to coeliac disease among those with potential disease. However, a negative screening test was associated with a very low risk for a clinical diagnosis within a follow-up period of 5 years.

Indexed as

Celiac DiseaseDiabetes Mellitus, Type 1BiopsyChildFollow-Up StudiesHumansMass Screeningepidemiologygastroenterologypaediatrics

Identifiers

PMID34921003
PMCPMC9125362
OpenAlexW4200494796

What OpenQuestion holds

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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.