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Food protein‐induced enterocolitis syndrome: A large French multicentric experience

BACKGROUND: Food protein‐induced enterocolitis syndrome (FPIES) is a non‐IgE‐mediated food allergy, with potential dehydration secondary to vomiting. Differences exist regarding culprit foods, and age of tolerance depending on the country of origin. We aimed at describing the characteristics of a Fr...

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Autores principales: Lemoine, Anaïs, Colas, Anne‐Sophie, Le, Sébastien, Delacourt, Christophe, Tounian, Patrick, Lezmi, Guillaume
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850996/
https://www.ncbi.nlm.nih.gov/pubmed/35218323
http://dx.doi.org/10.1002/clt2.12112
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author Lemoine, Anaïs
Colas, Anne‐Sophie
Le, Sébastien
Delacourt, Christophe
Tounian, Patrick
Lezmi, Guillaume
author_facet Lemoine, Anaïs
Colas, Anne‐Sophie
Le, Sébastien
Delacourt, Christophe
Tounian, Patrick
Lezmi, Guillaume
author_sort Lemoine, Anaïs
collection PubMed
description BACKGROUND: Food protein‐induced enterocolitis syndrome (FPIES) is a non‐IgE‐mediated food allergy, with potential dehydration secondary to vomiting. Differences exist regarding culprit foods, and age of tolerance depending on the country of origin. We aimed at describing the characteristics of a French population of children with FPIES, and define risk factors for failure during challenge. METHODS: Data from 179 children who were referred for FPIES in two pediatric tertiary centers between 2014 and 2020 were retrospectively collected. The diagnosis of FPIES was based on international consensus guidelines. Clinical characteristics, culprit food, and age at resolution were assessed. Tolerance was defined as no adverse reaction after OFC or accidental exposure. RESULTS: In the 192 described FPIES, the age at first symptoms was 5.8 months old. The main offending foods were cow's milk (60.3%), hen's egg (16.2%), and fish (11.7%). Single FPIES was observed in 94.4% and multiple FPIES in 5.6% of cases. The age at resolution of FPIES was 2.2 years old, and resolution occurred later for fish than for milk (2.9 years vs. 2.0, p = 0.01). Severe acute FPIES was a risk factor for delayed resolution (RR: 3.3 [1.2–9.2]), but not IgE sensitization. Performing a food challenge within 12 months after the first reaction increased the risk of failure (OR: 2.6 [1.1–6.6]). CONCLUSION: In this French cohort of children with FPIES, the main culprit foods were ubiquitous. Rice, oat, and soy were rarely or not involved. Multiple FPIES was infrequent. Our data confirmed the overall good prognosis of FPIES, the later resolution of FPIES to fish and in the case of severe acute FPIES.
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spelling pubmed-88509962022-02-25 Food protein‐induced enterocolitis syndrome: A large French multicentric experience Lemoine, Anaïs Colas, Anne‐Sophie Le, Sébastien Delacourt, Christophe Tounian, Patrick Lezmi, Guillaume Clin Transl Allergy Original Article BACKGROUND: Food protein‐induced enterocolitis syndrome (FPIES) is a non‐IgE‐mediated food allergy, with potential dehydration secondary to vomiting. Differences exist regarding culprit foods, and age of tolerance depending on the country of origin. We aimed at describing the characteristics of a French population of children with FPIES, and define risk factors for failure during challenge. METHODS: Data from 179 children who were referred for FPIES in two pediatric tertiary centers between 2014 and 2020 were retrospectively collected. The diagnosis of FPIES was based on international consensus guidelines. Clinical characteristics, culprit food, and age at resolution were assessed. Tolerance was defined as no adverse reaction after OFC or accidental exposure. RESULTS: In the 192 described FPIES, the age at first symptoms was 5.8 months old. The main offending foods were cow's milk (60.3%), hen's egg (16.2%), and fish (11.7%). Single FPIES was observed in 94.4% and multiple FPIES in 5.6% of cases. The age at resolution of FPIES was 2.2 years old, and resolution occurred later for fish than for milk (2.9 years vs. 2.0, p = 0.01). Severe acute FPIES was a risk factor for delayed resolution (RR: 3.3 [1.2–9.2]), but not IgE sensitization. Performing a food challenge within 12 months after the first reaction increased the risk of failure (OR: 2.6 [1.1–6.6]). CONCLUSION: In this French cohort of children with FPIES, the main culprit foods were ubiquitous. Rice, oat, and soy were rarely or not involved. Multiple FPIES was infrequent. Our data confirmed the overall good prognosis of FPIES, the later resolution of FPIES to fish and in the case of severe acute FPIES. John Wiley and Sons Inc. 2022-02-17 /pmc/articles/PMC8850996/ /pubmed/35218323 http://dx.doi.org/10.1002/clt2.12112 Text en © 2022 The Authors. Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lemoine, Anaïs
Colas, Anne‐Sophie
Le, Sébastien
Delacourt, Christophe
Tounian, Patrick
Lezmi, Guillaume
Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title_full Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title_fullStr Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title_full_unstemmed Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title_short Food protein‐induced enterocolitis syndrome: A large French multicentric experience
title_sort food protein‐induced enterocolitis syndrome: a large french multicentric experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850996/
https://www.ncbi.nlm.nih.gov/pubmed/35218323
http://dx.doi.org/10.1002/clt2.12112
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