Evidence map›Paper›PMID 37600614›Full record

Trial reportJPGN reports2023

Low Levels of Detectable Urine and Stool GIPs in Children with Celiac Disease on a Gluten-Free Diet.

Maxwell Horton, Katherine L Olshan, Elizabeth Gleeson, Stephanie Regis, Taylor Morson, Zackary J Hintze, Maureen M Leonard, Jocelyn A Silvester

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in JPGN reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 23% 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, 4 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 3 institutions in 1 country.

Maxwell HortonFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Katherine L OlshanFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Elizabeth GleesonMucosal Immunology and Biology Research Center, MassGeneral Hospital for Children, Boston, Massachusetts, USA.
Stephanie RegisFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Taylor MorsonMucosal Immunology and Biology Research Center, MassGeneral Hospital for Children, Boston, Massachusetts, USA.
Zackary J HintzeFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Maureen M LeonardFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Jocelyn A SilvesterFrom the Celiac Research Program, Harvard Medical School, Boston, Massachusetts, USA.
Harvard University · USBoston Children's Hospital · USMassachusetts General Hospital · US

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Prospective Multi-Omic Analysis of At-Risk infants to Model Celiac Disease PathogenesisK23DK122127 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI LEONARD, MAUREEN MICHELLE · 2019 to 2023
$1.2M
Mechanisms and Markers of Small Intestinal Epithelial Injury and Villous AtrophyK23DK119584 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI SILVESTER, JOCELYN ANNE · 2019 to 2023
$971k
NCATS NIH HHS UL1 TR002541NIDDK NIH HHS K23 DK119584NIDDK NIH HHS K23 DK122127
6 · The paper itself

Abstract

Objectives: This study examines the prevalence of detectable gluten immunogenic peptides (GIPs) as a proxy for gluten exposure in children with celiac disease on a gluten-free diet in the United States, as estimated by gluten breakdown products excreted in urine and stool. Methods: Urine and stool samples were collected in 3 settings (home, gastroenterology clinic, and endoscopy) for pediatric participants (ages 6-21 years old) across 2 medical centers. Commercial ELISA assays were used to quantify the GIPs in each sample. Results: GIPs were detected in 4 out of 44 (9.1%) of stool samples and 6 out of 125 (4.8%) of urine samples provided by 84 children. These samples were collected across all settings, and most participants (70%) were asymptomatic at the time of sample collection. For the urine samples collected at the time of endoscopy, all subjects found to have persistent enteropathy had no detectable GIPs (0/12). Discussion: GIPs provide an additional method for screening for gluten exposures in individuals with celiac disease on a gluten-free diet, and may be used across multiple settings. We found a low detection rate of GIPs in children. Our finding of undetectable GIPs in individuals with persistent enteropathy may be expected of a single determination under close observation or represent a lack of gluten exposure within the detection window. More research is needed to understand the dynamics of gluten absorption and excretion in the US pediatric population.

Identifiers

PMID37600614
PMCPMC10435043
OpenAlexW4379981235

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.