Evidence map›Paper›PMID 30311156›Full record

ArticleDigestive diseases and sciences2019

Prevalence and Clinical Features of Celiac Disease in Healthy School-Aged Children.

Omer Faruk Beser, Emine Gulluelli, Fugen Cullu Cokugras, Tulay Erkan, Tufan Kutlu, Rasit Vural Yagci, Firuze Erbek Alp, Gulten Ercal, Nuray Kepil, Mine Kucur and 1 more

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Article in Digestive diseases and sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 2 pooled it
–field-weighted citation impact, top 80% 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, 2 syntheses or guidelines pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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

11 authors at 3 institutions in 2 countries.

Omer Faruk BeserDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Health Sciences, Okmeydani Education and Training Hospital, Istanbul, Turkey. ofbeser@gmail.com.
Emine GulluelliDirector of Basic Health Care Office, Northern Cyprus Ministry of Health, Nicosia, Cyprus.
Fugen Cullu CokugrasDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Tulay ErkanDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Tufan KutluDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Rasit Vural YagciDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Ege University Medical Faculty, Izmir, Turkey.
Firuze Erbek AlpDepartment of Pediatrics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Gulten ErcalCyprus Turkish Pediatric Association, Nicosia, Cyprus.
Nuray KepilDepartment of Pathology, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Mine KucurDepartment of Medical Biochemistry, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
Northern Cyprus Celiac Study Group
Istanbul University-Cerrahpaşa · TREge University · TRSağlık Bilimleri Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsThe aim of this study was to determine the prevalence of celiac disease (CD) in healthy school-aged children in the northern region of Cyprus and to investigate the existence of potential markers that may accompany CD. This is the first study to measure the prevalence of CD in the northern region of Cyprus.

methodsThis study included 3792 school-aged children who were between the ages of 6 and 10 years between January 2015 and October 2016. CD was screened using total serum IgA, IgA anti-tissue transglutaminase (tTG), and IgA antiendomysial (EMA) antibodies. Subjects with selective IgA deficiency were further tested for IgG-tTG. Small intestinal biopsies were performed on all subjects with tTG antibody positivity. Risk factors and symptoms related to CD were evaluated using questionnaires in both the CD and control groups.

resultsOf the 3792 subjects, 39 were antibody positive (IgA-tTG was positive only in 14 subjects, IgA-tTG plus IgA-EMA in 21 subjects, and IgG-tTG in 4 subjects). IgA deficiency was detected in 11 subjects (0.29%). IgG-tTG was positive in 4 subjects with IgA deficiency (36.3%). Intestinal biopsies were performed on 28 of the 39 seropositive subjects. The biopsy findings of 15 children were consistent with CD (IgA-tTG positive in 3, IgA-tTG and IgA-EMA positive in 10, and IgG-tTG positive in 2). Thus, biopsies confirmed CD in 1:256 children (0.39%).

conclusionsOur study, which is the first study of school-aged children from the northern region of Cyprus, revealed that CD is a prevalent disease in this region.

Indexed as

Age of OnsetAutoantibodiesBiopsyCase-Control StudiesCeliac DiseaseChildCyprusFemaleGTP-Binding ProteinsHumansIgA DeficiencyImmunoglobulin AImmunoglobulin GIntestine, SmallMalePrevalenceAutoantibodiesGTP-Binding ProteinsImmunoglobulin AImmunoglobulin GProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesCeliac diseaseChildrenIgA anti-tissue transglutaminasePrevalence

Identifiers

PMID30311156
OpenAlexW2895796567

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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.