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Leskien, Miriam ORCID logoORCID: https://orcid.org/0009-0004-6884-6640; Scheerer, Martin; Thiering, Elisabeth ORCID logoORCID: https://orcid.org/0000-0002-5429-9584; Kress, Sara ORCID logoORCID: https://orcid.org/0000-0002-8007-5357; Coffey, Claire ORCID logoORCID: https://orcid.org/0000-0001-6915-1139; Berdel, Dietrich; Berg, Andrea von; Bauer, Carl‐Peter; Gappa, Monika ORCID logoORCID: https://orcid.org/0009-0006-8001-1165; Heinrich, Joachim ORCID logoORCID: https://orcid.org/0000-0002-9620-1629; Koletzko, Sibylle ORCID logoORCID: https://orcid.org/0000-0003-2374-8778; Schikowski, Tamara; Koletzko, Berthold ORCID logoORCID: https://orcid.org/0000-0002-5345-7165; Peters, Annette ORCID logoORCID: https://orcid.org/0000-0001-6645-0985 und Standl, Marie ORCID logoORCID: https://orcid.org/0000-0002-5345-2049 (2026): Prediction of allergic disease trajectories from birth up to adolescence. In: Pediatric Allergy and Immunology, Vol. 37, No. 4, e70341 [PDF, 2MB]

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Abstract

Background: Allergic diseases often develop jointly during early childhood. Potential disease trajectories and relevant early-life factors have been described, yet existing prediction approaches mostly focus on single allergic diseases cross-sectionally. Models addressing allergic multimorbidity and disease trajectories are lacking. We aim to predict allergic disease trajectories from birth up to adolescence using early-life factors.

Methods: Preceding research using data from 4646 adolescents of the German birth cohorts GINIplus and LISA identified seven allergic disease trajectories up to the age of 15 years. A set of predictors comprising parental and perinatal factors, early allergic or respiratory symptoms, lifestyle and environmental factors was used with an XGBoost machine learning approach to perform multiclass classification. In a subsample (N = 2109), polygenic risk scores (PRS) for asthma, allergic rhinitis, atopic dermatitis, and any allergy were added to the predictor set.

Results: Our approach revealed moderate classification success (multiclass area under the curve (AUC) = 0.69). A macro-averaged sensitivity of 0.26 and specificity of 0.89 were obtained. The most important predictors were early-life skin rash, respiratory symptoms, and air pollution. In the sub-analysis, the PRS were among the factors with high importance, but the prediction performance in external test data was not improved.

Conclusions: Our prediction success was comparable to established prediction scores while accounting for multiple allergic disease trajectories and using solely early-life factors. This study cannot yet provide reliable individual-level prediction in a clinical setting but can inform development of future work on this.

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