Emollients for prevention of atopic dermatitis: 5-year findings from the BEEP randomized trial.


Journal

Allergy
ISSN: 1398-9995
Titre abrégé: Allergy
Pays: Denmark
ID NLM: 7804028

Informations de publication

Date de publication:
04 2023
Historique:
revised: 14 09 2022
received: 15 07 2022
accepted: 22 09 2022
medline: 4 4 2023
pubmed: 21 10 2022
entrez: 20 10 2022
Statut: ppublish

Résumé

The effectiveness of emollients for preventing atopic dermatitis/eczema is controversial. The Barrier Enhancement for Eczema Prevention trial evaluated the effects of daily emollients during the first year of life on atopic dermatitis and atopic conditions to age 5 years. 1394 term infants with a family history of atopic disease were randomized (1:1) to daily emollient plus standard skin-care advice (693 emollient group) or standard skin-care advice alone (701 controls). Long-term follow-up at ages 3, 4 and 5 years was via parental questionnaires. Main outcomes were parental report of a clinical diagnosis of atopic dermatitis and food allergy. Parents reported more frequent moisturizer application in the emollient group through to 5 years. A clinical diagnosis of atopic dermatitis between 12 and 60 months was reported for 188/608 (31%) in the emollient group and 178/631 (28%) in the control group (adjusted relative risk 1.10, 95% confidence interval 0.93 to 1.30). Although more parents in the emollient group reported food reactions in the previous year at 3 and 4 years, cumulative incidence of doctor-diagnosed food allergy by 5 years was similar between groups (92/609 [15%] emollients and 87/632 [14%] controls, adjusted relative risk 1.11, 95% confidence interval 0.84 to 1.45). Findings were similar for cumulative incidence of asthma and hay fever. Daily emollient application during the first year of life does not prevent atopic dermatitis, food allergy, asthma or hay fever.

Sections du résumé

BACKGROUND
The effectiveness of emollients for preventing atopic dermatitis/eczema is controversial. The Barrier Enhancement for Eczema Prevention trial evaluated the effects of daily emollients during the first year of life on atopic dermatitis and atopic conditions to age 5 years.
METHODS
1394 term infants with a family history of atopic disease were randomized (1:1) to daily emollient plus standard skin-care advice (693 emollient group) or standard skin-care advice alone (701 controls). Long-term follow-up at ages 3, 4 and 5 years was via parental questionnaires. Main outcomes were parental report of a clinical diagnosis of atopic dermatitis and food allergy.
RESULTS
Parents reported more frequent moisturizer application in the emollient group through to 5 years. A clinical diagnosis of atopic dermatitis between 12 and 60 months was reported for 188/608 (31%) in the emollient group and 178/631 (28%) in the control group (adjusted relative risk 1.10, 95% confidence interval 0.93 to 1.30). Although more parents in the emollient group reported food reactions in the previous year at 3 and 4 years, cumulative incidence of doctor-diagnosed food allergy by 5 years was similar between groups (92/609 [15%] emollients and 87/632 [14%] controls, adjusted relative risk 1.11, 95% confidence interval 0.84 to 1.45). Findings were similar for cumulative incidence of asthma and hay fever.
CONCLUSIONS
Daily emollient application during the first year of life does not prevent atopic dermatitis, food allergy, asthma or hay fever.

Identifiants

pubmed: 36263451
doi: 10.1111/all.15555
doi:

Substances chimiques

Emollients 0

Banques de données

ISRCTN
['ISRCTN21528841']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

995-1006

Subventions

Organisme : Department of Health
ID : 12/67/12
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

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Auteurs

Lucy E Bradshaw (LE)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Laura A Wyatt (LA)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Sara J Brown (SJ)

Skin Research Group, School of Medicine, University of Dundee, Dundee, UK.
Department of Dermatology, Ninewells Hospital and Medical School, Dundee, UK.

Rachel H Haines (RH)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Alan A Montgomery (AA)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Michael R Perkin (MR)

Population Health Research Institute, St. George's University of London, London, UK.

Sandra Lawton (S)

Rotherham NHS Foundation Trust, UK.

Tracey H Sach (TH)

Health Economics Group, Norwich Medical School, University of East Anglia, Norwich, UK.

Joanne R Chalmers (JR)

Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.

Matthew J Ridd (MJ)

Population Health Sciences, University of Bristol, Bristol, UK.

Carsten Flohr (C)

Unit for Population-Based Dermatology Research, St John's Institute of Dermatology, Guy's & St Thomas' NHS Foundation Trust and King's College London, London, UK.

Joanne Brooks (J)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Richard Swinden (R)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Eleanor J Mitchell (EJ)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Stella Tarr (S)

Nottingham Clinical Trials Unit, School of Medicine, University of Nottingham, Nottingham, UK.

Nicola Jay (N)

Sheffield Children's Hospital, Sheffield, UK.

Kim S Thomas (KS)

Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.

Hilary Allen (H)

National Heart and Lung Institute, Imperial College London, London, UK.

Michael J Cork (MJ)

Sheffield Dermatology Research, Department of Infection and Immunity, University of Sheffield, Sheffield, UK.

Maeve M Kelleher (MM)

National Heart and Lung Institute, Imperial College London, London, UK.

Eric L Simpson (EL)

Department of Dermatology, Oregon Health & Science University, Portland, Oregon, USA.

Stella T Lartey (ST)

Health Economics Group, Norwich Medical School, University of East Anglia, Norwich, UK.

Susan Davies-Jones (S)

Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.

Robert J Boyle (RJ)

Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.
National Heart and Lung Institute, Imperial College London, London, UK.

Hywel C Williams (HC)

Centre of Evidence Based Dermatology, School of Medicine, University of Nottingham, Nottingham, UK.

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