Serological Investigation of Persistent Villous Atrophy in Celiac Disease.


Journal

Clinical and translational gastroenterology
ISSN: 2155-384X
Titre abrégé: Clin Transl Gastroenterol
Pays: United States
ID NLM: 101532142

Informations de publication

Date de publication:
27 Sep 2023
Historique:
received: 27 03 2023
accepted: 05 09 2023
medline: 27 9 2023
pubmed: 27 9 2023
entrez: 27 9 2023
Statut: aheadofprint

Résumé

Persistent villous atrophy (VA) is not uncommon in celiac disease (CeD) while patients take a gluten-free diet (GFD). We conducted a retrospective study with 122 serum samples collected from controls and CeD patients either at the initial diagnosis or follow-up during endoscopy. These samples were assigned to three groups: non-celiac control, non-VA CeD (Marsh score 0-2), and VA CeD (Marsh score 3a-3c). We established an in-house multiplex assay to identify potential serological biomarkers for villous atrophy. We assessed autoantibodies reported to affect the small intestine, including IgA and IgG antibodies against tissue transglutaminase (tTG), interferons, villin, actin, autoimmune enteropathy-related 75 kDa antigen (AIE-75), and tryptophan hydroxylase (TPH)-1, as well as 27 cytokines. The apolipoproteins quantified included apo A1, apo B-100, and apo A4, which were produced predominantly by the intestinal epithelium or expressed specifically in villi. Autoantibody levels were high only for tTG antibodies, which performed well in initial CeD diagnosis, but suboptimally for VA prediction during follow-up, as 14.6% of the follow-up patients with VA had low tTG-IgA. Increasing dilution improved tTG-IgA quantification, particularly when the antibody levels were extremely high, but did not significantly improve VA detection. Among those with low tTG-IgA and persistent VA, high proinflammatory cytokines were observed in two patients. Median LDL-C levels were significantly lower in the VA CeD group (P = 0.03). Apolipoprotein levels were similar in patients with and without VA, but diverged between those on a gluten-free diet (GFD) or not.Conclusions: tTG-IgA as a biomarker is suboptimal for villous atrophy prediction while on a GFD. Persistent villous atrophy is associated with low LDL-C levels, and partially related to persistent high proinflammatory cytokines.

Identifiants

pubmed: 37753949
doi: 10.14309/ctg.0000000000000639
pii: 01720094-990000000-00197
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : K08DK128631
Pays : United States

Informations de copyright

Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology.

Auteurs

Changlin Gong (C)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.

Claudia Saborit (C)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.

Xin Long (X)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.

Ao Wang (A)

. Department of Medicine, Celiac Disease Center, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.

Beishi Zheng (B)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.

Howard Chung (H)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.

Suzanne K Lewis (SK)

. Department of Medicine, Celiac Disease Center, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.

Suneeta Krishnareddy (S)

. Department of Medicine, Celiac Disease Center, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.

Govind Bhagat (G)

. Department of Medicine, Celiac Disease Center, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.
. Department of Pathology and Cell Biology, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.

Peter H R Green (PHR)

. Department of Medicine, Celiac Disease Center, New York Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY 10032.

Xiao-Fei Kong (XF)

. Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX, 75235.
. McDermott Center for Human Growth and Development, UT Southwestern Medical Center, Dallas, TX, 75390.

Classifications MeSH