Affiliation:
1. Nomura Dermatology Clinic Yokohama Japan
2. Advanced Data Science Project, RIKEN Information R&D and Strategy Headquarters, RIKEN Yokohama Japan
3. Collective Intelligence Research Laboratory, Graduate School of Arts and Sciences The University of Tokyo Tokyo Japan
4. Department of Extended Intelligence for Medicine, The Ishii‐Ishibashi Laboratory Keio University School of Medicine Tokyo Japan
Abstract
AbstractBackgroundPersistent facial erythema represents a significant complication in atopic dermatitis (AD) patients undergoing treatment with dupilumab. Stratifying patients based on the erythema course is crucial for elucidating heterogeneous phenotypes and facilitating advanced drug efficacy predictions.ObjectivesThis study aimed to identify factors associated with facial erythema severity in dupilumab‐treated AD patients and to establish a prediction model for drug response based on the identified factors.MethodsData from a retrospective study conducted between July 2018 and July 2021 were collected and analysed. Patients were categorized into three groups via hierarchical clustering based on the course of facial erythema: early remission, low remission and persistent residual. LightGBM, a supervised gradient boosting decision tree algorithm, was employed to discern group differences and construct a prediction model. The model incorporated patient demographic and clinical profiles, including pre‐ and post‐treatment examinations. The model's performance was evaluated using accuracy and the area under the receiver operating characteristic curve (AUC).ResultsThe binary classification model demonstrated an accuracy of 89.10% and an AUC of 0.862 when distinguishing between early remission and persistent residual patients. The eight prominent factors associated with facial erythema severity included age, sex, lactate dehydrogenase (LDH), immunoglobulin E (IgE), eosinophil count, white blood cell count, Alnus allergy and cedar allergy.ConclusionsThis study has two main significances: first, three clusters were identified through unsupervised learning; second, a classification model was constructed that proved more accurate than random prediction. The stratification and identification of crucial factors associated with residual facial erythema in dupilumab‐treated AD patients lay the foundation for AI‐powered prognostic models. This groundwork provides a substantial basis for enhancing future medical AI support in AD treatment selection, potentially improving personalized treatment approaches and outcomes.
Funder
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development