Evidence map›Paper›PMID 41695077›Full record

ArticleJPGN reports2026

Autoantibody signatures in children with celiac disease, juvenile idiopathic arthritis, and polyautoimmunity.

Nan Du, Denis Chang, Madison Wong, Jay R Thiagarajah, Erin Janssen, Lauren A Henderson, Krishnan Raghunathan, Jocelyn A Silvester

Abstract read
In one paragraph

Article in JPGN reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

8 authors.

Nan DuDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0002-2728-917X
Denis ChangDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.
Madison WongDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.
Jay R ThiagarajahDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.
Erin JanssenDepartment of Pediatrics, Michigan Medicine, C.S. Mott Children's Hospital University of Michigan Medical School Ann Arbor Michigan USA.
Lauren A HendersonDivision of Immunology Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.
Krishnan RaghunathanDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.
Jocelyn A SilvesterDivision of Gastroenterology and Nutrition Boston Children's Hospital, Harvard Medical School Boston Massachusetts USA.

Funding

TRAINING IN PEDIATRIC GASTROENTEROLOGY &NUTRITIONT32DK007477 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI Scott B Snapper · 1986 to 2026
$13.3M
Joint Biology Consortium Resource-based CenterP30AR070253 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter A Nigrovic, Jeffrey Andrew Sparks · 2016 to 2026
$9.4M
Instrumenting the Delivery System for a Genomics Research Information CommonsU01TR002623 · NCATS · BOSTON CHILDREN'S HOSPITAL · PI MANDL, KENNETH D. · 2019 to 2024
$8.6M
T peripheral regulatory cells as modulators of T cell-B cell interactions in arthritisR01AR083424 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI Lauren A Henderson · 2024 to 2026
$1.5M
NCATS NIH HHS U01 TR002623NIAMS NIH HHS P30 AR070253NIAMS NIH HHS R01 AR083424NIDDK NIH HHS T32 DK007477
6 · The paper itself

Abstract

Objective: To determine if multiplex autoantibody arrays can identify novel biomarker signatures in children with one or multiple autoimmune diseases (polyautoimmunity). Methods: Plasma collected from children (18 years or younger) in the Boston Children's Hospital Precision Link Biobank for Health Discovery between January 2007 and June 2021 was analyzed using a microarray with 120 autoantigens associated with various autoimmune diseases to assess for both immunoglobulin G (IgG) and A (IgA) autoantibodies. To determine if disease-specific, we binary classified those with polyautoimmunity and the most common autoimmune diseases in our cohort (autoimmune thyroid disease, type 1 diabetes, or celiac disease [CeD]). For each comparison within and between groups, the autoantibody intensity was releveled to the control and a linear model was fit. Results: Plasma was analyzed from 114 children with either CeD ( Conclusions: Use of multiplex antigen arrays in patients with and without polyautoimmunity is a valuable tool to identify known and potentially novel disease-antigens. Further study is needed to determine the role of H/K ATPase autoantibodies in monitoring of CeD patients.

Indexed as

autoimmune disordersbiomarkersmultiplex arrays

Identifiers

PMID41695077
PMCPMC12894067

What Socratic 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 Socratic graph.