Allergen immunotherapy for atopic dermatitis: Systematic review and meta-analysis of benefits and harms.

Atopic dermatitis (atopic eczema) DLQI GRADE approach SCORAD adverse events aeroallergen allergen immunotherapy (AIT) allergy evidence-based medicine house dust mite itch (pruritus) meta-analysis multidisciplinary quality of life sleep disturbance subcutaneous immunotherapy (SCIT) sublingual immunotherapy (SLIT) systematic review

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:
01 2023
Historique:
received: 29 04 2022
revised: 22 08 2022
accepted: 01 09 2022
pubmed: 4 10 2022
medline: 11 1 2023
entrez: 3 10 2022
Statut: ppublish

Résumé

Atopic dermatitis (AD, eczema) is driven by a combination of skin barrier defects, immune dysregulation, and extrinsic stimuli such as allergens, irritants, and microbes. The role of environmental allergens (aeroallergens) in triggering AD remains unclear. We systematically synthesized evidence regarding the benefits and harms of allergen immunotherapy (AIT) for AD. As part of the 2022 American Academy of Allergy, Asthma & Immunology/American College of Allergy, Asthma and Immunology Joint Task Force on Practice Parameters AD Guideline update, we searched the MEDLINE, EMBASE, CENTRAL, CINAHL, LILACS, Global Resource for Eczema Trials, and Web of Science databases from inception to December 2021 for randomized controlled trials comparing subcutaneous immunotherapy (SCIT), sublingual immunotherapy (SLIT), and/or no AIT (placebo or standard care) for guideline panel-defined patient-important outcomes: AD severity, itch, AD-related quality of life (QoL), flares, and adverse events. Raters independently screened, extracted data, and assessed risk of bias in duplicate. We synthesized intervention effects using frequentist and Bayesian random-effects models. The GRADE approach determined the quality of evidence. Twenty-three randomized controlled trials including 1957 adult and pediatric patients sensitized primarily to house dust mite showed that add-on SCIT and SLIT have similar relative and absolute effects and likely result in important improvements in AD severity, defined as a 50% reduction in SCORing Atopic Dermatitis (risk ratio [95% confidence interval] 1.53 [1.31-1.78]; 26% vs 40%, absolute difference 14%) and QoL, defined as an improvement in Dermatology Life Quality Index by 4 points or more (risk ratio [95% confidence interval] 1.44 [1.03-2.01]; 39% vs 56%, absolute difference 17%; both outcomes moderate certainty). Both routes of AIT increased adverse events (risk ratio [95% confidence interval] 1.61 [1.44-1.79]; 66% with SCIT vs 41% with placebo; 13% with SLIT vs 8% with placebo; high certainty). AIT's effect on sleep disturbance and eczema flares was very uncertain. Subgroup and sensitivity analyses were consistent with the main findings. SCIT and SLIT to aeroallergens, particularly house dust mite, can similarly and importantly improve AD severity and QoL. SCIT increases adverse effects more than SLIT. These findings support a multidisciplinary and shared decision-making approach to optimally managing AD.

Sections du résumé

BACKGROUND
Atopic dermatitis (AD, eczema) is driven by a combination of skin barrier defects, immune dysregulation, and extrinsic stimuli such as allergens, irritants, and microbes. The role of environmental allergens (aeroallergens) in triggering AD remains unclear.
OBJECTIVE
We systematically synthesized evidence regarding the benefits and harms of allergen immunotherapy (AIT) for AD.
METHODS
As part of the 2022 American Academy of Allergy, Asthma & Immunology/American College of Allergy, Asthma and Immunology Joint Task Force on Practice Parameters AD Guideline update, we searched the MEDLINE, EMBASE, CENTRAL, CINAHL, LILACS, Global Resource for Eczema Trials, and Web of Science databases from inception to December 2021 for randomized controlled trials comparing subcutaneous immunotherapy (SCIT), sublingual immunotherapy (SLIT), and/or no AIT (placebo or standard care) for guideline panel-defined patient-important outcomes: AD severity, itch, AD-related quality of life (QoL), flares, and adverse events. Raters independently screened, extracted data, and assessed risk of bias in duplicate. We synthesized intervention effects using frequentist and Bayesian random-effects models. The GRADE approach determined the quality of evidence.
RESULTS
Twenty-three randomized controlled trials including 1957 adult and pediatric patients sensitized primarily to house dust mite showed that add-on SCIT and SLIT have similar relative and absolute effects and likely result in important improvements in AD severity, defined as a 50% reduction in SCORing Atopic Dermatitis (risk ratio [95% confidence interval] 1.53 [1.31-1.78]; 26% vs 40%, absolute difference 14%) and QoL, defined as an improvement in Dermatology Life Quality Index by 4 points or more (risk ratio [95% confidence interval] 1.44 [1.03-2.01]; 39% vs 56%, absolute difference 17%; both outcomes moderate certainty). Both routes of AIT increased adverse events (risk ratio [95% confidence interval] 1.61 [1.44-1.79]; 66% with SCIT vs 41% with placebo; 13% with SLIT vs 8% with placebo; high certainty). AIT's effect on sleep disturbance and eczema flares was very uncertain. Subgroup and sensitivity analyses were consistent with the main findings.
CONCLUSIONS
SCIT and SLIT to aeroallergens, particularly house dust mite, can similarly and importantly improve AD severity and QoL. SCIT increases adverse effects more than SLIT. These findings support a multidisciplinary and shared decision-making approach to optimally managing AD.

Identifiants

pubmed: 36191689
pii: S0091-6749(22)01322-7
doi: 10.1016/j.jaci.2022.09.020
pii:
doi:

Substances chimiques

Allergens 0

Types de publication

Meta-Analysis Systematic Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-158

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Juan José Yepes-Nuñez (JJ)

Universidad de Los Andes, Bogota; Fundacion Santa Fe de Bogota University, Bogota.

Gordon H Guyatt (GH)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton; Department of Health Research Methods, Evidence and Impact, Hamilton.

Luis Guillermo Gómez-Escobar (LG)

Universidad de Los Andes, Bogota.

Lucia C Pérez-Herrera (LC)

Universidad de Los Andes, Bogota.

Alexandro W L Chu (AWL)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Renata Ceccaci (R)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Ana Sofía Acosta-Madiedo (AS)

Universidad de Los Andes, Bogota.

Aaron Wen (A)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Sergio Moreno-López (S)

Universidad de Los Andes, Bogota.

Margaret MacDonald (M)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Mónica Barrios (M)

Universidad de Los Andes, Bogota.

Xiajing Chu (X)

Department of Health Research Methods, Evidence and Impact, Hamilton; Evidence-Based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou.

Nazmul Islam (N)

Department of Health Research Methods, Evidence and Impact, Hamilton; Department of Public Health, College of Health Sciences, QU Health, Qatar University, Doha.

Ya Gao (Y)

Department of Health Research Methods, Evidence and Impact, Hamilton; Evidence-Based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou.

Melanie M Wong (MM)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Rachel Couban (R)

Department of Health Research Methods, Evidence and Impact, Hamilton.

Elizabeth Garcia (E)

Fundacion Santa Fe de Bogota University, Bogota.

Edgardo Chapman (E)

Fundacion Santa Fe de Bogota University, Bogota.

Paul Oykhman (P)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton.

Lina Chen (L)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton; University of Ottawa, Ottawa.

Tonya Winders (T)

Allergy & Asthma Network, Vienna.

Rachel Netahe Asiniwasis (RN)

Origins Dermatology Centre, University of Saskatchewan, Regina.

Mark Boguniewicz (M)

National Jewish Health, Denver; University of Colorado School of Medicine, Aurora.

Anna De Benedetto (A)

Department of Dermatology, University of Rochester Medical Center, Rochester.

Kathy Ellison (K)

Westerville.

Winfred T Frazier (WT)

Department of Family Medicine, UPMC St Margaret, Pittsburgh.

Matthew Greenhawt (M)

University of Colorado School of Medicine, Aurora.

Joey Huynh (J)

Orthopedic Neurological Rehabilitation, Northridge.

Jennifer LeBovidge (J)

Boston Children's Hospital, Harvard Medical School, Boston.

Mary Laura Lind (ML)

School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe.

Peter Lio (P)

Northwestern University Feinberg School of Medicine, Chicago.

Stephen A Martin (SA)

University of Massachusetts Chan Medical School, Worcester.

Monica O'Brien (M)

Tufts University School of Medicine, Boston.

Peck Y Ong (PY)

Children's Hospital Los Angeles, University of Southern California, Los Angeles.

Jonathan I Silverberg (JI)

Department of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington.

Jonathan Spergel (J)

Division of Allergy and Immunology, Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine at University of of Pennsylvania, Philadelphia.

Julie Wang (J)

Icahn School of Medicine at Mount Sinai, New York.

Kathryn E Wheeler (KE)

Department of Pediatrics, University of Florida, Gainesville.

Lynda Schneider (L)

Boston Children's Hospital, Harvard Medical School, Boston.

Derek K Chu (DK)

Department of Medicine, McMaster University, and Evidence in Allergy Group, Hamilton; Department of Health Research Methods, Evidence and Impact, Hamilton; Research Institute of St Joe's Hamilton, Hamilton. Electronic address: chudk@mcmaster.ca.

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