Fecal gluten immunogenic peptides as indicators of dietary compliance in celiac patients.


Journal

Minerva gastroenterologica e dietologica
ISSN: 1827-1642
Titre abrégé: Minerva Gastroenterol Dietol
Pays: Italy
ID NLM: 9109791

Informations de publication

Date de publication:
Sep 2020
Historique:
pubmed: 29 3 2020
medline: 9 7 2021
entrez: 29 3 2020
Statut: ppublish

Résumé

It is important to have methods for evaluating dietary compliance in patients with celiac disease (CD). Determination of fecal gluten immunogenic peptides (GIPs) was recently proposed as a method of detecting gluten intake. The aim of this study was to evaluate whether determination of GIPs can be used as an indicator of compliance with a gluten-free diet (GFD). Twenty-five persons with CD on a gluten-free diet for at least one year were enrolled in the study. Compliance with the diet was assessed by the Biagi questionnaire, evaluation of symptoms and assay of IgA anti-tissue transglutaminase antibodies (IgA anti-tTG). GIPs were determined by iVYLISA GIP-S test (Biomedal S.L., Seville, Spain) on an automated Chorus analyzer (DIESSE Diagnostica Senese, Siena, Italy), after extraction of fecal samples by the method developed by DIESSE. Four patients tested positive for GIPs (GIP+), two of whom complied strictly with the gluten-free diet according to the Biagi questionnaire. None of the four GIP-positive patients manifested symptoms. IgA anti-tTG was significantly higher in GIP+ than in GIP- subjects. Assay of fecal GIPs identified more patients who were not complying with the diet than the Biagi questionnaire or evaluation of symptoms. The anti-tTG and GIP results agreed perfectly; however, since anti-tTG antibodies remain high for longer and are not a completely reliable marker of GFD intake, detection of fecal GIPs offers a direct, objective, quantitative assessment of exposure, even occasional, to gluten and could be used to check dietary compliance.

Sections du résumé

BACKGROUND BACKGROUND
It is important to have methods for evaluating dietary compliance in patients with celiac disease (CD). Determination of fecal gluten immunogenic peptides (GIPs) was recently proposed as a method of detecting gluten intake. The aim of this study was to evaluate whether determination of GIPs can be used as an indicator of compliance with a gluten-free diet (GFD).
METHODS METHODS
Twenty-five persons with CD on a gluten-free diet for at least one year were enrolled in the study. Compliance with the diet was assessed by the Biagi questionnaire, evaluation of symptoms and assay of IgA anti-tissue transglutaminase antibodies (IgA anti-tTG). GIPs were determined by iVYLISA GIP-S test (Biomedal S.L., Seville, Spain) on an automated Chorus analyzer (DIESSE Diagnostica Senese, Siena, Italy), after extraction of fecal samples by the method developed by DIESSE.
RESULTS RESULTS
Four patients tested positive for GIPs (GIP+), two of whom complied strictly with the gluten-free diet according to the Biagi questionnaire. None of the four GIP-positive patients manifested symptoms. IgA anti-tTG was significantly higher in GIP+ than in GIP- subjects.
CONCLUSIONS CONCLUSIONS
Assay of fecal GIPs identified more patients who were not complying with the diet than the Biagi questionnaire or evaluation of symptoms. The anti-tTG and GIP results agreed perfectly; however, since anti-tTG antibodies remain high for longer and are not a completely reliable marker of GFD intake, detection of fecal GIPs offers a direct, objective, quantitative assessment of exposure, even occasional, to gluten and could be used to check dietary compliance.

Identifiants

pubmed: 32218420
pii: S1121-421X.20.02662-8
doi: 10.23736/S1121-421X.20.02662-8
doi:

Substances chimiques

Autoantibodies 0
Immunoglobulin A 0
Peptides 0
Glutens 8002-80-0
Protein Glutamine gamma Glutamyltransferase 2 EC 2.3.2.13
Transglutaminases EC 2.3.2.13
GTP-Binding Proteins EC 3.6.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

201-207

Auteurs

Brunetta Porcelli (B)

Section of Biochemistry, Department of Medical Biotechnologies, University of Siena, Siena, Italy - brunetta.porcelli@unisi.it.

Fabio Ferretti (F)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Francesca Cinci (F)

Section of Biochemistry, Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Ivano Biviano (I)

Unit of Gastroenterology and Operative Endoscopy, Siena University Hospital, Siena, Italy.

Alessia Santini (A)

Unit of Gastroenterology and Operative Endoscopy, Siena University Hospital, Siena, Italy.

Elisabetta Grande (E)

Unit of Pediatrics, Siena University Hospital, Siena, Italy.

Francesco Quagliarella (F)

Unit of Pediatrics, Siena University Hospital, Siena, Italy.

Lucia Terzuoli (L)

Section of Biochemistry, Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Maria R Bacarelli (MR)

Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.

Nicola Bizzaro (N)

Laboratory of Clinical Pathology, San Antonio Hospital Tolmezzo, Udine Integrated University Healthcare Company, Udine, Italy.

Marina Vascotto (M)

Unit of Pediatrics, Siena University Hospital, Siena, Italy.

Mario Marini (M)

Unit of Gastroenterology and Operative Endoscopy, Siena University Hospital, Siena, Italy.

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Classifications MeSH