Enhanced early skin treatment for atopic dermatitis in infants reduces food allergy.


Journal

The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 17 11 2022
revised: 20 02 2023
accepted: 07 03 2023
medline: 10 7 2023
pubmed: 25 3 2023
entrez: 24 3 2023
Statut: ppublish

Résumé

Early-onset atopic dermatitis is a strong risk factor for food allergy, suggesting that early effective treatment may prevent transcutaneous sensitization. This study tested whether enhanced treatment of atopic dermatitis to clinically affected and unaffected skin is more effective in preventing hen's egg allergy than reactive treatment to clinically affected skin only. This was a multicenter, parallel-group, open-label, assessor-blind, randomized controlled trial (PACI [Prevention of Allergy via Cutaneous Intervention] study). This study enrolled infants 7-13 weeks old with atopic dermatitis and randomly assigned infants in a 1:1 ratio to enhanced early skin treatment or conventional reactive treatment using topical corticosteroids (TCSs). The primary outcome was the proportion of immediate hen's egg allergy confirmed by oral food challenge at 28 weeks of age. This study enrolled 650 infants and analyzed 640 infants (enhanced [n = 318] or conventional [n = 322] treatment). Enhanced treatment significantly reduced hen's egg allergy compared with the conventional treatment (31.4% vs 41.9%, P = .0028; risk difference: -10.5%, upper bound of a 1-sided CI: -3.0%), while it lowered body weight (mean difference: -422 g, 95% CI: -553 to -292 g) and height (mean difference: -0.8 cm, 95% CI: -1.22 to -0.33 cm) at 28 weeks of age. This study highlighted the potential of well-controlled atopic dermatitis management as a component of a hen's egg allergy prevention strategy. The enhanced treatment protocol of this trial should be modified before it can be considered as an approach to prevent hen's egg allergy in daily practice to avoid the adverse effects of TCSs. After remission induction by TCSs, maintenance therapy with lower potency TCSs or other topical therapies might be considered as alternative proactive treatments to overcome the safety concerns of TCSs.

Sections du résumé

BACKGROUND BACKGROUND
Early-onset atopic dermatitis is a strong risk factor for food allergy, suggesting that early effective treatment may prevent transcutaneous sensitization.
OBJECTIVES OBJECTIVE
This study tested whether enhanced treatment of atopic dermatitis to clinically affected and unaffected skin is more effective in preventing hen's egg allergy than reactive treatment to clinically affected skin only.
METHODS METHODS
This was a multicenter, parallel-group, open-label, assessor-blind, randomized controlled trial (PACI [Prevention of Allergy via Cutaneous Intervention] study). This study enrolled infants 7-13 weeks old with atopic dermatitis and randomly assigned infants in a 1:1 ratio to enhanced early skin treatment or conventional reactive treatment using topical corticosteroids (TCSs). The primary outcome was the proportion of immediate hen's egg allergy confirmed by oral food challenge at 28 weeks of age.
RESULTS RESULTS
This study enrolled 650 infants and analyzed 640 infants (enhanced [n = 318] or conventional [n = 322] treatment). Enhanced treatment significantly reduced hen's egg allergy compared with the conventional treatment (31.4% vs 41.9%, P = .0028; risk difference: -10.5%, upper bound of a 1-sided CI: -3.0%), while it lowered body weight (mean difference: -422 g, 95% CI: -553 to -292 g) and height (mean difference: -0.8 cm, 95% CI: -1.22 to -0.33 cm) at 28 weeks of age.
CONCLUSIONS CONCLUSIONS
This study highlighted the potential of well-controlled atopic dermatitis management as a component of a hen's egg allergy prevention strategy. The enhanced treatment protocol of this trial should be modified before it can be considered as an approach to prevent hen's egg allergy in daily practice to avoid the adverse effects of TCSs. After remission induction by TCSs, maintenance therapy with lower potency TCSs or other topical therapies might be considered as alternative proactive treatments to overcome the safety concerns of TCSs.

Identifiants

pubmed: 36963619
pii: S0091-6749(23)00331-7
doi: 10.1016/j.jaci.2023.03.008
pii:
doi:

Substances chimiques

Dermatologic Agents 0

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-135

Investigateurs

Kumiko Morita (K)
Eisuke Inoue (E)
Tatsuki Fukuie (T)
Shigenori Kabashima (S)
Yusuke Inuzuka (Y)
Koji Nishimura (K)
Kenji Toyokuni (K)
Hiroya Ogita (H)
Tomoyuki Kiguchi (T)
Kazue Yoshida (K)
Jumpei Saito (J)
Hajime Hosoi (H)
Norito Katoh (N)
Mariko Morimoto (M)
Koji Masuda (K)
Makoto Kameda (M)
Amane Shigekawa (A)
Koji Yamasaki (K)
Megumi Nagai (M)
Motohiro Ebisawa (M)
Tomoyuki Asaumi (T)
Takaaki Itonaga (T)
Shunji Hasegawa (S)
Hiroki Yasudo (H)
Mizuho Nagao (M)
Takao Fujisawa (T)
Ryuhei Yasuoka (R)
Toshiharu Fujiyama (T)
Naoki Shimojo (N)
Taiji Nakano (T)
Yasuto Kondo (Y)
Yuji Mori (Y)
Takahiro Kawaguchi (T)
Masaki Futamura (M)
Kazumitsu Sugiura (K)
Akiyo Nagai (A)
Sachiko Kaburagi (S)
Hiroshi Kitazawa (H)
Hiroshi Kido (H)
Shoji F Nakayama (SF)

Informations de copyright

Copyright © 2023 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Kiwako Yamamoto-Hanada (K)

National Center for Child Health and Development, Tokyo, Japan.

Tohru Kobayashi (T)

National Center for Child Health and Development, Tokyo, Japan.

Masashi Mikami (M)

National Center for Child Health and Development, Tokyo, Japan.

Hywel C Williams (HC)

Centre of Evidence-Based Dermatology, University of Nottingham, Nottingham, United Kingdom.

Hirohisa Saito (H)

National Center for Child Health and Development, Tokyo, Japan.

Mayako Saito-Abe (M)

National Center for Child Health and Development, Tokyo, Japan.

Miori Sato (M)

National Center for Child Health and Development, Tokyo, Japan.

Makoto Irahara (M)

National Center for Child Health and Development, Tokyo, Japan.

Yumiko Miyaji (Y)

National Center for Child Health and Development, Tokyo, Japan.

Fumi Ishikawa (F)

National Center for Child Health and Development, Tokyo, Japan.

Kunihiko Tsuchiya (K)

Kyoto Prefectural University of Medicine, Kyoto, Japan.

Risa Tamagawa-Mineoka (R)

Kyoto Prefectural University of Medicine, Kyoto, Japan.

Yuri Takaoka (Y)

Osaka Habikino Medical Center, Osaka, Japan.

Yutaka Takemura (Y)

Kindai University Faculty of Medicine, Osaka, Japan.

Sakura Sato (S)

National Hospital Organization Sagamihara National Hospital, Kanagawa, Japan.

Hiroyuki Wakiguchi (H)

Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.

Miyuki Hoshi (M)

National Hospital Organization Mie National Hospital, Mie, Japan.

Osamu Natsume (O)

Hamamatsu University School of Medicine, Shizuoka, Japan.

Fumiya Yamaide (F)

Chiba University Graduate School of Medicine, Chiba, Japan.

Miwako Seike (M)

National Center for Child Health and Development, Tokyo, Japan.

Yukihiro Ohya (Y)

National Center for Child Health and Development, Tokyo, Japan. Electronic address: ohya-y@ncchd.go.jp.

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Classifications MeSH