Researchers say early-warning models could help target preventive care
Children who develop eczema very early in life often go on to face other allergic conditions, but clinicians have had limited tools for estimating which patients are most likely to progress to more serious respiratory disease. A new study suggests that machine learning may now offer a sharper way to sort that risk.
In research published online April 17 in the Journal of Allergy and Clinical Immunology, investigators from Kaiser Permanente Southern California developed and validated prediction models for children diagnosed with atopic dermatitis before age 3. Using electronic health record data from 10,688 children, the team built models to estimate individualized risk for developing moderate-to-severe persistent asthma and allergic rhinitis between ages 5 and 11.
The results point to a potentially useful clinical tool, especially for health systems looking to identify higher-risk children earlier and intervene before symptoms escalate. The researchers reported strong performance for asthma prediction and more moderate, but still meaningful, performance for allergic rhinitis.
Strong asthma prediction in a large real-world dataset
The asthma models posted area-under-the-curve scores of 0.893 for the comprehensive version and 0.892 for a simplified version, indicating strong discrimination in separating children who later developed disease from those who did not. At a 95% specificity threshold, the comprehensive model achieved 40.4% sensitivity and a positive predictive value of 39.3%, while the simplified model reached 36.2% sensitivity and 33.8% positive predictive value.
Those figures matter because they suggest the models were particularly good at limiting false positives while still capturing a meaningful share of children who would later go on to develop persistent asthma. In practice, such a balance can be important for pediatric care, where unnecessary escalation has costs, but missed risk can lead to delayed treatment and avoidable complications.
The rhinitis models were less precise than the asthma models, but still delivered moderate predictive performance. The comprehensive rhinitis model achieved an AUC of 0.793, while the simplified model scored 0.773. At 90% specificity, the comprehensive model reached 35.5% sensitivity with a 72.7% positive predictive value, while the simplified model produced 34.0% sensitivity and 69.2% positive predictive value.
The authors also reported acceptable calibration, with especially strong agreement in the highest-risk groups. That point is significant because even a model with strong discrimination can be less useful if its risk estimates are poorly aligned with what actually happens in the clinic.







