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Prevalence and characteristics of peanut allergy in US adults - 03/06/21

Doi : 10.1016/j.jaci.2020.11.046 
Christopher Warren, PhD a, b, , Dawn Lei, MD c, d, , Scott Sicherer, MD e, Robert Schleimer, PhD c, Ruchi Gupta, MD, MPH a, d,
a Center for Food Allergy and Asthma Research, Northwestern University Feinberg School of Medicine, Chicago, Ill 
b Sean N. Parker Center for Allergy and Asthma Research, Stanford University School of Medicine, Stanford, Calif 
c Division of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Ill 
d Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Ill 
e Elliot and Roslyn Jaffe Food Allergy Institute, Division of Allergy, Department of Pediatrics, Mount Sinai School of Medicine, New York, NY 

Corresponding author: Ruchi S. Gupta, MD, 750 N Lake Shore Drive, Suite 680 Chicago, IL 60611.750 N Lake Shore DriveSuite 680ChicagoIL60611

Abstract

Background

Peanut allergy (PA) is the leading pediatric food allergy and a common cause of anaphylaxis. Little is known, however, on the prevalence and characteristics of PA in the adult population and whether phenotypic differences exist between adult-onset and childhood-onset PA.

Objectives

This study describes the current US population-level burden of adult PA.

Methods

A cross-sectional food allergy survey was administered via phone and web in 2015 and 2016, resulting in nationally representative complex-survey weighted data for 40,443 adults. Reported food allergies were considered “convincing” if symptoms to specific allergens were consistent with an IgE-mediated reaction.

Results

The prevalence of current self-reported PA was 2.9% among US adults, with 1.8% having convincing PA. Over 17% of adults with peanut allergy reported onset of their PA in adulthood. In adults with childhood-onset PA, 75.4% reported physician-diagnosed PA, compared with only 58.9% of adult-onset PA. Despite a similar frequency of food allergy–related emergency department visits within the past year (approximately 1 in 5 adults with PA allergy), adults with childhood-onset PA were significantly more likely to have a current epinephrine prescription compared with those with adult-onset PA (56% vs 44% respectively; P = .02) and were more likely to use an epinephrine autoinjector (48% vs 35%, P = .01).

Conclusions

Approximately 4.6 million US adults have PA—over 800,000 of whom appear to have developed their PA after age 18 years. Further examination of phenotypic differences between childhood-onset and adult-onset PA may improve understanding and management of adult PA.

Le texte complet de cet article est disponible en PDF.

Key words : Food allergy, atopy, peanut allergy, prevalence, adult-onset food allergy

Abbreviations used : EAI, ED, OAS, PA, sIgE, SPT


Plan


 Supported by grant R21AI135702-PI from the National Institute of Allergy and Infectious Diseases.
 Disclosure of potential conflict of interest: R. S. Gupta reports receiving grants from the National Institutes of Health (grants R21 ID# AI135705, R01 ID# AI130348, and U01 ID# AI138907), Rho Inc, Stanford Sean N. Parker Center for Allergy Research, UnitedHealth Group, Thermo Fisher Scientific, Genentech, and the National Confectioners Association; and serves as a medical consultant/advisor for Before Brands, Kaléo Inc, Genentech, Institute for Clinical and Economic Review, Food Allergy Research and Education, Aimmune Therapeutics, and DBV Technologies. S. Sicherer reports royalty payments from UpToDate and from Johns Hopkins University Press; grants to his institution from the National Institute of Allergy and Infectious Diseases, from Food Allergy Research and Education, and from HAL Allergy; and personal fees from the American Academy of Allergy, Asthma and Immunology, outside of the submitted work. S. Sicherer was the American Academy of Pediatrics representative to the National Institute of Allergy and Infectious Diseases Expert Panel for peanut allergy guidelines and also co-author of American Academy of Pediatrics Clinical Reports regarding atopy prevention. R. Schleimer reports National Institutes of Health grant money paid to the institution and to himself, and consulting fees and/or stock ownership from Intersect ENT, GlaxoSmithKline, Allakos, Aurasense, Merck, BioMarck, Sanofi, AstraZeneca/Medimmune, Genetech, Exicure, Otsuka, Aqualung Therapeutics Corp, Actobio Therapeutics, Lyra Therapeutics, Astellas Pharm Inc, and Genzyme/Sanofi Corp; and has Siglec-8 and Siglec-8 ligand-related patents licensed to Allakos Inc. The rest of the authors declare that they have no relevant conflicts of interest.


© 2021  Publié par Elsevier Masson SAS.
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Vol 147 - N° 6

P. 2263 - juin 2021 Retour au numéro
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