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Development of a prediction model for infants at high risk of food allergy

BACKGROUND: Identification of risk factors for food allergy (FA) in infants is an active research area. An important reason is to identify optimal target infants for early introduction of specific food antigens. Although eczema has been used for this purpose, multivariable prediction scores have not...

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Autores principales: Sugiura, Shiro, Hiramitsu, Yoshimichi, Futamura, Masaki, Kamioka, Naomi, Yamaguchi, Chikae, Umemura, Harue, Ito, Komei, Camargo, Carlos A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870367/
https://www.ncbi.nlm.nih.gov/pubmed/33604275
http://dx.doi.org/10.5415/apallergy.2021.11.e5
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author Sugiura, Shiro
Hiramitsu, Yoshimichi
Futamura, Masaki
Kamioka, Naomi
Yamaguchi, Chikae
Umemura, Harue
Ito, Komei
Camargo, Carlos A.
author_facet Sugiura, Shiro
Hiramitsu, Yoshimichi
Futamura, Masaki
Kamioka, Naomi
Yamaguchi, Chikae
Umemura, Harue
Ito, Komei
Camargo, Carlos A.
author_sort Sugiura, Shiro
collection PubMed
description BACKGROUND: Identification of risk factors for food allergy (FA) in infants is an active research area. An important reason is to identify optimal target infants for early introduction of specific food antigens. Although eczema has been used for this purpose, multivariable prediction scores have not been reported. OBJECTIVE: The aim of this research is to develop a multivariable prediction score for infants at high risk of FA. METHODS: We performed a cross-sectional analysis of a self-administered questionnaire for the parents of 18-month-old children at well-child visits between April 2016 and March 2017 (development dataset) and between April 2017 and March 2018 (validation dataset). We developed and validated the prediction score. RESULTS: The questionnaire collection rate was 18,549 of 20,198 (92%) in the development dataset and 18,620 of 19,977 (93%) in the validation dataset. Risk factors for FA were being born in August–December, first child, eczema, atopic dermatitis in father and mother, and FA in mother and sibling(s). For identifying infants with FA, the developed multivariable prediction score showed higher discrimination ability (area under the curve [AUC] = 0.75) than focusing on eczema (AUC = 0.70) in the validation dataset. The score was also useful for identifying infants with a history of anaphylaxis (AUC = 0.73) than focusing on eczema (AUC = 0.67) in the validation dataset. CONCLUSION: The new prediction score enables more efficient identification of infants at high risk of FA, who may be the optimal target group for the early introduction of specific antigens.
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spelling pubmed-78703672021-02-17 Development of a prediction model for infants at high risk of food allergy Sugiura, Shiro Hiramitsu, Yoshimichi Futamura, Masaki Kamioka, Naomi Yamaguchi, Chikae Umemura, Harue Ito, Komei Camargo, Carlos A. Asia Pac Allergy Original Article BACKGROUND: Identification of risk factors for food allergy (FA) in infants is an active research area. An important reason is to identify optimal target infants for early introduction of specific food antigens. Although eczema has been used for this purpose, multivariable prediction scores have not been reported. OBJECTIVE: The aim of this research is to develop a multivariable prediction score for infants at high risk of FA. METHODS: We performed a cross-sectional analysis of a self-administered questionnaire for the parents of 18-month-old children at well-child visits between April 2016 and March 2017 (development dataset) and between April 2017 and March 2018 (validation dataset). We developed and validated the prediction score. RESULTS: The questionnaire collection rate was 18,549 of 20,198 (92%) in the development dataset and 18,620 of 19,977 (93%) in the validation dataset. Risk factors for FA were being born in August–December, first child, eczema, atopic dermatitis in father and mother, and FA in mother and sibling(s). For identifying infants with FA, the developed multivariable prediction score showed higher discrimination ability (area under the curve [AUC] = 0.75) than focusing on eczema (AUC = 0.70) in the validation dataset. The score was also useful for identifying infants with a history of anaphylaxis (AUC = 0.73) than focusing on eczema (AUC = 0.67) in the validation dataset. CONCLUSION: The new prediction score enables more efficient identification of infants at high risk of FA, who may be the optimal target group for the early introduction of specific antigens. Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2021-01-22 /pmc/articles/PMC7870367/ /pubmed/33604275 http://dx.doi.org/10.5415/apallergy.2021.11.e5 Text en Copyright © 2021. Asia Pacific Association of Allergy, Asthma and Clinical Immunology. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sugiura, Shiro
Hiramitsu, Yoshimichi
Futamura, Masaki
Kamioka, Naomi
Yamaguchi, Chikae
Umemura, Harue
Ito, Komei
Camargo, Carlos A.
Development of a prediction model for infants at high risk of food allergy
title Development of a prediction model for infants at high risk of food allergy
title_full Development of a prediction model for infants at high risk of food allergy
title_fullStr Development of a prediction model for infants at high risk of food allergy
title_full_unstemmed Development of a prediction model for infants at high risk of food allergy
title_short Development of a prediction model for infants at high risk of food allergy
title_sort development of a prediction model for infants at high risk of food allergy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870367/
https://www.ncbi.nlm.nih.gov/pubmed/33604275
http://dx.doi.org/10.5415/apallergy.2021.11.e5
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