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. 2024 Oct;79(10):2748-2758.
doi: 10.1111/all.16265. Epub 2024 Aug 21.

Evaluation of dupilumab on the disease burden in children and adolescents with atopic dermatitis: A population-based cohort study

Affiliations

Evaluation of dupilumab on the disease burden in children and adolescents with atopic dermatitis: A population-based cohort study

Serena Yun-Chen Tsai et al. Allergy. 2024 Oct.

Abstract

Background: Dupilumab is the first and only biologic agent approved for the treatment of atopic dermatitis (AD) in pediatric patients aged from 6 months to 17 years. The study aimed to evaluate the impact of dupilumab on the occurrence of comorbidities in pediatric patients with AD.

Methods: In this population-based cohort study, we utilized electronic health records from multiple healthcare organizations across the United States. Pediatric patients (<18 years of age) with a diagnosis of AD initiating dupilumab were propensity-score matched 1:1 to those initiating other systemic agents (azathioprine, cyclosporine, methotrexate, mycophenolate mofetil, or systemic corticosteroids). The primary outcomes were new-onset comorbidities emerging during the study period measured by the risk ratio (RR) and its confidence interval (CI). Subgroup analyses were stratified by age (0-5 years, 6-11 years, and 12-17 years), sex, and race.

Results: A total of 3575 pediatric patients with AD treated with dupilumab were matched to 3575 patients treated with other systemic agents. The dupilumab cohort was associated with a lowered risk of new-onset atopic comorbidities (including asthma [RR, 0.72; 95% CI, 0.59-0.89] and allergic rhinitis [RR, 0.62; 95% CI, 0.52-0.74]), infections (e.g., skin and soft tissue infection [RR, 0.70; 95% CI, 0.63-0.76] and respiratory tract infection [RR = 0.56; 95% CI, 0.51-0.61]), psychiatric disorders (e.g., mood disorder [RR, 0.52; 95% CI, 0.39-0.70] and anxiety [RR, 0.57; 95% CI, 0.46-0.70], sleep disturbance [RR, 0.60; 95% CI, 0.47-0.77]), neurologic and developmental disorders (e.g., attention deficit hyperactivity disorder [RR, 0.54; 95% CI, 0.38-0.75]). Furthermore, the positive effects are found to be more pronounced in younger children (aged 0-5 years) with AD.

Conclusions: Treatment with dupilumab compared to systemic agents resulted in reductions in AD-related comorbidities in pediatric patients.

Keywords: adolescents; atopic dermatitis; atopic march; biologics; children; comorbidities; dupilumab; infections; mental health; neurodevelopmental disorders.

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Conflict of interest statement

Dr. Gaffin receives research funding from GSK and AstraZeneca.

Dr. Hawryluk receives royalty from UpToDate (author/reviewer), and reports conflicts with Apogee (advisory board) and Skin Analytics (consulting).

Dr. Oyoshi was supported by grants NIH/NIAID R01 AI142872, R01 AI172938, and R21 AI151591.

Dr. Schneider: Investigator – Regeneron, DBV Technologies. Advisory Boards - Sanofi, Triveni Bio, DBV, Alladapt Immunotherapeutics, BioThea Pharmaceuticals, Ukko, Leo pharmaceuticals, DAIT/NIAID, National Eczema Association

Dr. Phipatanakul was supported by grant NIH/NIAID K24 AI106822.

Dr. Tsai, Hana Ruran, Dr. Bartnikas, and Dr. Ma have no COI to report.

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