Atopic dermatitis: Correlation of distinct risk factors with age of onset in adulthood compared to childhood

Laura Maintz, Marie Therese Schmitz, Nadine Herrmann, Svenja Müller, Regina Havenith, Juliette Brauer, Claudio Rhyner, Anita Dreher, Eugen Bersuch, Danielle Fehr, Gertrud Hammel, Matthias Reiger, Daria Luschkova, Avidan Neumann, Claudia C.V. Lang, Ellen D. Renner, Peter Schmid-Grendelmeier, Claudia Traidl-Hoffmann, Cezmi A. Akdis, Roger LauenerMarie Charlotte Brüggen, Matthias Schmid, Thomas Bieber

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Background: Atopic dermatitis (AD) has long been regarded as a primarily pediatric disease. However, there is growing evidence for a high rate of adult-onset AD. We aimed to characterize factors associated with adult-onset versus childhood-onset AD and controls. Methods: We analyzed cross-sectional data of the CK-CARE-ProRaD cohorts Bonn, Augsburg, Davos, Zürich of 736 adult patients stratified by age of AD onset (childhood-onset <18 years: 76.4% (subsets: 0 to 2; ≥2 to 6; ≥7 to 11; ≥12 to 18); adult-onset ≥18 years: 23.6% (subsets: ≥18 to 40; ≥41 to 60; ≥61) and 167 controls (91 atopic, 76 non-atopic)). Results: We identified active smoking to be associated with adult-onset AD versus controls (adjusted Odds Ratio (aOR) = 5.54 [95% Confidence Interval: 1.06–29.01] vs. controlsnon-atopic, aOR = 4.03 [1.20–13.45] vs. controlsatopic). Conjunctivitis showed a negative association versus controlsatopic (aOR = 0.36 [0.14–0.91]). Food allergy (aOR = 2.93 [1.44–5.96]), maternal food allergy (aOR = 9.43 [1.10–80.95]), palmar hyperlinearity (aOR = 2.11 [1.05–4.25]), and academic background (aOR = 2.14 [1.00–4.54]) increased the odds of childhood-onset AD versus controlsatopic. Shared AD-associated factors were maternal AD (4-34x), increased IgE (2-20x), atopic stigmata (2-3x) with varying effect sizes depending on AD onset and control group. Patients with adult-compared to childhood-onset had doubled odds of allergic rhinitis (aOR = 2.15 [1.12–4.13]), but reduced odds to feature multiple (3–4) atopic comorbidities (aOR = 0.34 [0.14–0.84]). Adult-onset AD, particularly onset ≥61 years, grouped mainly in clusters with low contributions of personal and familial atopy and high frequencies of physical inactivity, childhood-onset AD, particularly infant-onset, mainly in “high-atopic”-clusters. Conclusions: The identified associated factors suggest partly varying endo- and exogeneous mechanisms underlying adult-onset versus childhood-onset AD. Our findings might contribute to better assessment of the individual risk to develop AD throughout life and encourage prevention by non-smoking and physical activity as modifiable lifestyle factors.

Original languageEnglish
Pages (from-to)2181-2201
Number of pages21
JournalAllergy: European Journal of Allergy and Clinical Immunology
Volume78
Issue number8
Early online date22 Mar 2023
DOIs
StatePublished - Aug 2023
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

Funding

We thank the Christine Kühne‐Center for Allergy Research and Education (CK‐CARE), Davos, Switzerland for funding of the study. Laura Maintz, Marie‐Therese Schmitz, Juliette Brauer, Svenja Müller, Regina Havenith, Claudio Rhyner, Anita Dreher, Eugen Bersuch, Daria Luschkova and Ellen D Renner were or are supported by, or were or are employees of CK‐CARE. Marie‐Charlotte Brüggen is supported by CK‐CARE. The funding sources did not participate in the study design and conduct, nor in the data collection, management, analysis, and interpretation, nor in preparation, review or approval of the manuscript nor in the decision to submit the article for publication.

FundersFunder number
Christine Kühne – Center for Allergy Research and Education

    Keywords

    • adult-onset
    • associated factor
    • atopic dermatitis
    • childhood-onset
    • phenotype

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