Detection and quantification of gluten immunogenic peptides in feces of infants and their relationship with diet.


Journal

Revista espanola de enfermedades digestivas
ISSN: 1130-0108
Titre abrégé: Rev Esp Enferm Dig
Pays: Spain
ID NLM: 9007566

Informations de publication

Date de publication:
Feb 2019
Historique:
pubmed: 16 10 2018
medline: 10 3 2020
entrez: 16 10 2018
Statut: ppublish

Résumé

there are no effective methods to easily control the correct adherence to a gluten-free diet (GFD) in celiac disease (CD) patients. to assess the sensitivity and specificity of a rapid immunochromatographic (IC) test that detects gluten immunogenic peptides (GIP) in feces, compared to an enzyme-linked immunosorbent assay (ELISA) method. fecal samples from healthy infants were analyzed by a rapid IC test and ELISA, both methods are based on the anti-gliadin 33-mer monoclonal antibody. Group 1 included infants aged from 6 to 24 months, with an unrestricted consumption of gluten containing cereals. Group 2 (negative controls) was comprised of infants aged from 0 to 6 months, either breastfed or formula fed who had never ingested gluten. in group 1 (n = 34), all infants had positive values by ELISA, the mean was 13.13 μgGIP/g (range 0.56-46.79). The IC test was negative in 5/20 cases and there was a significant correlation (p=0.006) between the mean daily gluten intake and GIP in feces. In group 2 (n = 20), all the samples were negative by both methods. Moreover, the Kappa Fleiss concordance index (Kappa = 0.79 CI95% [0.616, 0.965]) indicated a moderate concordance between both methods. according to our results, both methods are highly specific. However, the ELISA test had a higher sensitivity. Although we found a significant correlation between the amount of gluten consumed and GIP recovery in feces, further studies are needed to clarify the impact of individual confounding factors in GIP recovery.

Sections du résumé

BACKGROUND BACKGROUND
there are no effective methods to easily control the correct adherence to a gluten-free diet (GFD) in celiac disease (CD) patients.
AIM OBJECTIVE
to assess the sensitivity and specificity of a rapid immunochromatographic (IC) test that detects gluten immunogenic peptides (GIP) in feces, compared to an enzyme-linked immunosorbent assay (ELISA) method.
METHODS METHODS
fecal samples from healthy infants were analyzed by a rapid IC test and ELISA, both methods are based on the anti-gliadin 33-mer monoclonal antibody. Group 1 included infants aged from 6 to 24 months, with an unrestricted consumption of gluten containing cereals. Group 2 (negative controls) was comprised of infants aged from 0 to 6 months, either breastfed or formula fed who had never ingested gluten.
RESULTS RESULTS
in group 1 (n = 34), all infants had positive values by ELISA, the mean was 13.13 μgGIP/g (range 0.56-46.79). The IC test was negative in 5/20 cases and there was a significant correlation (p=0.006) between the mean daily gluten intake and GIP in feces. In group 2 (n = 20), all the samples were negative by both methods. Moreover, the Kappa Fleiss concordance index (Kappa = 0.79 CI95% [0.616, 0.965]) indicated a moderate concordance between both methods.
CONCLUSIONS CONCLUSIONS
according to our results, both methods are highly specific. However, the ELISA test had a higher sensitivity. Although we found a significant correlation between the amount of gluten consumed and GIP recovery in feces, further studies are needed to clarify the impact of individual confounding factors in GIP recovery.

Identifiants

pubmed: 30318895
doi: 10.17235/reed.2018.5549/2018
doi:

Substances chimiques

Antibodies, Monoclonal 0
Glutens 8002-80-0
Gliadin 9007-90-3

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106-110

Auteurs

María Roca (M)

U. Enfermedad Celiaca e Inmunopatología Digestiva, Instituto de Investigación Sanitaria La Fe, España.

Ester Donat (E)

Gastroenterología y Hepatología Pediátrica,, Hospital Universitario y Politécnico La Fe,, España,.

Etna Masip (E)

Gastroenterología y Hepatología Pediátrica,, Hospital Universitario y Politécnico La Fe,, España.

Paula Crespo Escobar (P)

Unidad de Enfermedad Celiaca e Inmunopatología Dig, Instituto de Investigación Sanitaria la Fe, España.

Victoria Fornes-Ferrer (V)

Unidad de Bioestadística, Instituto de Investigación Sanitaria La Fe, España.

Begoña Polo (B)

Gastroenterología y Hepatología Pediátrica,, Hospital Universitario y Politécnico La Fe,, Valencia.

Carmen Ribes-Koninckx (C)

Gastroenterología y Hepatología Pediátrica,, Hospital Universitario y Politécnico La Fe,, España.

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Classifications MeSH