Evidence map›Paper›PMID 35564413›Full record

ArticleInternational journal of environmental research and public health2022

Evaluation of Celiac Disease by Minimally Invasive Biomarkers in a Spanish Pediatric Population.

Julia María Cabo Del Riego, María Jesús Núñez Iglesias, Carmen García-Plata González, José Paz Carreira, Tamara Álvarez Fernández, Ana Dorado Díaz, Noa Villar Mallo, Manuel Penedo Pita, Silvia Novío Mallón, Lola Máiz Suárez and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 4 institutions in 1 country.

Julia María Cabo Del RiegoClinical Analysis Laboratory, Department of Inmunology, Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.ORCID 0000-0002-6329-7409
María Jesús Núñez IglesiasDepartment of Psiquiatry, Radiology, Public Health, Nursing and Medicine, University of Santiago de Compostela, 15705 A Coruña, Spain.
Carmen García-Plata GonzálezPediatric Gastrohepathology Unit of Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
José Paz CarreiraPediatric Gastrohepathology Unit of Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
Tamara Álvarez FernándezClinical Analysis Laboratory, Department of Inmunology, Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
Ana Dorado DíazDepartment of Statistical Health Counselling, Junta de Castilla y León, 47001 Valladolid, Spain.
Noa Villar MalloClinical Analysis Laboratory, Department of Inmunology, Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
Manuel Penedo PitaClinical Analysis Laboratory, Department of Inmunology, Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
Silvia Novío MallónDepartment of Psiquiatry, Radiology, Public Health, Nursing and Medicine, University of Santiago de Compostela, 15705 A Coruña, Spain.ORCID 0000-0002-6169-8356
Lola Máiz SuárezClinical Analysis Laboratory, Department of Inmunology, Hospital Universitario Lucus Augusti, 27003 Lugo, Spain.
Manuel Freire-Garabal NúñezSNL Laboratory, School of Medicine and Dentistry, 15782 A Coruña, Spain.
Hospital Universitario Lucus Augusti · ESUniversidade da Coruña · ESJunta de Castilla y León · ESUniversidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of celiac disease (CD) has been substantially improved with the availability of highly sensitive CD-specific IgA-TG2, Ig-GDP, and IgA-EMA. The European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) published (2012) and updated (2020) diagnostic criteria for CD in order to simplify CD diagnosis and to avoid biopsies in selected patients.

methodsA prospective study including 5641 pediatric patients (0-16 years old) from January 2012 to January 2019 was performed. CD diagnosis was made according to the ESPGHAN algorithm. The objective of this study was to evaluate the utility of biomarkers and the relationship between TGA-IgA and EMA titers.

resultsCD diagnoses were confirmed in 113 patients, 110 were IgA-TG2-positive and 3 (2.7%) had IgA deficiency. The diagnosis was made by serologic tests in 95 (84.1%) patients. Only 18 (15.9%) patients underwent intestinal biopsy. We obtained 100% concordance between IgA-EMA and positive results for IgA-TG2 ≥ 10 ULN with IgA-EMA antibody titer ≥ 1:80.

conclusionsThis study provides evidence of a positive correlation between IgA-TG2 antibody serum levels and IgA-EMA. The diagnosis could be guaranteed with strict application of IgA-TG2 values ≥ 10 ULN (confirmed by subsequent testing) plus the serological response to the gluten-free diet (GFD).

Indexed as

Celiac DiseaseAdolescentAutoantibodiesBiomarkersChildChild, PreschoolHumansImmunoglobulin AInfantInfant, NewbornProspective StudiesTransglutaminasesAutoantibodiesBiomarkersImmunoglobulin ATransglutaminasesantibodiesceliac diseasediagnosisESPGHANnon-invasive biomarkerspediatric age

Identifiers

PMID35564413
PMCPMC9100138
OpenAlexW4224244512

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.