TY - JOUR
T1 - Development and Validation of the Risk of Exacerbation in Severe Asthma (RESA) Model
AU - Chen, Wenjia
AU - Lee, Tae Yoon
AU - Price, David
AU - Beasley, Richard
AU - Janson, Christer
AU - Siyue, Mariko Koh
AU - Yadav, Chandra Prakash
AU - Müllerová, Hana
AU - Burgel, Pierre Regis
AU - Tran, Trung N.
AU - Emmanuel, Benjamin
AU - Wang, Eileen
AU - Wechsler, Michael E.
AU - Jackson, David J.
AU - Busby, John
AU - Heaney, Liam G.
AU - Pfeffer, Paul E.
AU - Mahboub, Bassam
AU - Perng, Diahn Warng
AU - Cosio, Borja G.
AU - Perez-de-Llano, Luis
AU - Al-Lehebi, Riyad
AU - Larenas-Linnemann, Désirée
AU - Al-Ahmad, Mona
AU - Rhee, Chin Kook
AU - Iwanaga, Takashi
AU - Heffler, Enrico
AU - Canonica, Giorgio Walter
AU - Costello, Richard
AU - Papadopoulos, Nikolaos G.
AU - Papaioannou, Andriana I.
AU - Porsbjerg, Celeste M.
AU - Torres-Duque, Carlos A.
AU - Christoff, George C.
AU - Popov, Todor A.
AU - Hew, Mark
AU - Peters, Matthew
AU - Gibson, Peter G.
AU - Maspero, Jorge
AU - Bergeron, Celine
AU - Cerda, Saraid
AU - Contreras, Elvia Angelica
AU - Sadatsafavi, Mohsen
N1 - Publisher Copyright:
© 2026 The Authors
PY - 2026/7
Y1 - 2026/7
N2 - Background: Severe asthma (SA) is associated with frequent exacerbations and high treatment costs. Objectives: To develop and validate an individualized risk calculator for severe exacerbations in SA, and evaluate its clinical utility for guiding personalized clinical decisions. Methods: Patients with SA were identified from combined data from the International Severe Asthma Registry (2015-2022) and NOVEL observational longiTudinal studY (2016-2023) across 30 countries and regions. The prediction end point was the 12-month risk of 1 or more or 2 or more severe exacerbations. Using expert input and Bayesian network analysis, 11 routinely measured predictors were identified, measured within the past 12 months. A mixed-effects, zero-inflated negative binomial model was developed, adjusting for between-country variability and biologic drop-in effects. Internal-external cross-validation was performed using the natural clustering by country settings. Results: Data from 9911 patients with SA were used. Essential predictors included age, sex, past 12-month severe exacerbations, asthma control, chronic rhinosinusitis, FEV1 to forced vital capacity ratio, percent predicted FEV1, blood eosinophils, fractional exhaled nitric oxide, and long-term oral corticosteroid and macrolide use. The model also adapted setting-specific baseline risks. In the internal-external cross-validation, across broad geographical and health care variability, the model showed excellent calibration and informative, generalizable discrimination (pooled area under the time-dependent receiver-operating characteristics curve of 0.63 [95% CI, 0.60-0.66] for ≥1 and 0.68 [95% CI, 0.64-0.72] for ≥2 exacerbations). Decision curve analysis showed clear net benefit across risk thresholds. Conclusions: The Risk of Exacerbation in Severe Asthma model quantifies SA exacerbation risk using routinely available predictors and demonstrates potential clinical utility.
AB - Background: Severe asthma (SA) is associated with frequent exacerbations and high treatment costs. Objectives: To develop and validate an individualized risk calculator for severe exacerbations in SA, and evaluate its clinical utility for guiding personalized clinical decisions. Methods: Patients with SA were identified from combined data from the International Severe Asthma Registry (2015-2022) and NOVEL observational longiTudinal studY (2016-2023) across 30 countries and regions. The prediction end point was the 12-month risk of 1 or more or 2 or more severe exacerbations. Using expert input and Bayesian network analysis, 11 routinely measured predictors were identified, measured within the past 12 months. A mixed-effects, zero-inflated negative binomial model was developed, adjusting for between-country variability and biologic drop-in effects. Internal-external cross-validation was performed using the natural clustering by country settings. Results: Data from 9911 patients with SA were used. Essential predictors included age, sex, past 12-month severe exacerbations, asthma control, chronic rhinosinusitis, FEV1 to forced vital capacity ratio, percent predicted FEV1, blood eosinophils, fractional exhaled nitric oxide, and long-term oral corticosteroid and macrolide use. The model also adapted setting-specific baseline risks. In the internal-external cross-validation, across broad geographical and health care variability, the model showed excellent calibration and informative, generalizable discrimination (pooled area under the time-dependent receiver-operating characteristics curve of 0.63 [95% CI, 0.60-0.66] for ≥1 and 0.68 [95% CI, 0.64-0.72] for ≥2 exacerbations). Decision curve analysis showed clear net benefit across risk thresholds. Conclusions: The Risk of Exacerbation in Severe Asthma model quantifies SA exacerbation risk using routinely available predictors and demonstrates potential clinical utility.
KW - Clinical decision support
KW - Clinical utility
KW - Exacerbation risk
KW - Individualized risk
KW - Internal-external cross-validation
KW - Precision medicine
KW - Prediction model
KW - Real-world data
KW - Severe asthma
UR - https://www.scopus.com/pages/publications/105037534840
U2 - 10.1016/j.jaip.2026.03.017
DO - 10.1016/j.jaip.2026.03.017
M3 - Journal article
C2 - 41903878
AN - SCOPUS:105037534840
SN - 2213-2198
VL - 14
SP - 1589
EP - 1600
JO - Journal of Allergy and Clinical Immunology: In Practice
JF - Journal of Allergy and Clinical Immunology: In Practice
IS - 7
ER -