Pre-biologic disease trajectories are associated with morbidity burden and biologic treatment response in severe asthma

医学 哮喘 共病 疾病 内科学 儿科
作者
Marianne Baastrup Soendergaard,Frederikke Hjortdahl,Susanne Hansen,Anne‐Sofie Bjerrum,Anna von Bülow,Ole Hilberg,Barbara Bonnesen Bertelsen,Claus R. Johnsen,Sofie Lock Johansson,Roxana Vijdea,Linda Rasmussen,Johannes Martin Schmid,Charlotte Suppli Ulrik,Celeste Porsbjerg,Kjell Erik Julius Håkansson
出处
期刊:The European respiratory journal [European Respiratory Society]
卷期号:: 2401497-2401497
标识
DOI:10.1183/13993003.01497-2024
摘要

Background Biologics can induce remission in some patients with severe asthma, however, little is known about pre-biologic disease trajectories and their association with outcomes from biological treatment. We aimed to identify long-term trajectories of disease progression in patients initiating biologics and investigate trajectory associations with disease burden and impact on biologic therapy efficacy. Methods Patients in the Danish Severe Asthma Registry initiating biologic therapy between 2016–2022 were included and followed retrospectively in prescription databases starting 1995. We performed sequence analysis for inhaled corticosteroid (ICS) treatment intensity over time combined with unsupervised trajectory clustering. Results In total, 755 patients were included and three pre-biologic disease trajectories were identified: Chronic severe asthma (26%), Gradual onset severe asthma (35%), Recent, sudden onset severe asthma (39%). Chronic severe asthma patients were older, had the longest disease duration (35 years), the most impaired pulmonary function, the highest comorbidity prevalence and the lowest employment rate. Recent, sudden onset severe asthma patients were younger, had shorter disease duration (5 years), more tobacco exposure and the least impaired lung function. Gradual onset severe asthma had an intermediate burden of disease. The Chronic severe asthma cluster demonstrated the lowest prevalence of remission (17%) compared to the Gradual onset severe asthma (29%) and Recent onset severe asthma (32%) clusters. Conclusions Three pre-biologic disease trajectories were identified, with increased disease duration and activity associating with asthma- and comorbidity burden. Early intervention may be key to prevent irreversible adverse outcomes for patients with severe asthma.

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