TY - JOUR
T1 - Anti-Interleukin-5 Therapy Is Associated with Attenuated Lung Function Decline in Severe Eosinophilic Asthma Patients from the Belgian Severe Asthma Registry
AU - Graff, Sophie
AU - Brusselle, Guy G.
AU - Hanon, Shane Wendy
AU - Sohy, Carine
AU - Dupont, Lieven J
AU - Peché, Rudi
AU - Michils, Alain
AU - Pilette, Charles
AU - Joos, Guy
AU - Lahousse, Lies
AU - Lapperre, Thérèse
AU - Louis, Renaud
AU - Schleich, Florence N
PY - 2022/2
Y1 - 2022/2
N2 - Background: Asthmatics have accelerated lung function decline over time compared with healthy individuals. Objective: To evaluate risk factors for accelerated lung function decline. Methods: In a longitudinal analysis on severe asthmatics enrolled in the Belgian Severe Asthma Registry with at least 2 visits a minimum of 12 months apart, we compared characteristics of patients with and without decline (loss of post-bronchodilation forced expiratory volume in 1 s [FEV1] (% predicted)/y greater than zero) over time. Multiple linear regression was applied to study the factors independently associated with FEV1 decline. Results: In the overall population (n = 318), median annual FEV1 decline was 0.27 (–4.22 to 3.80) % predicted/y over a period of 23 months (12–41 months). Asthma was less controlled at baseline in nondecliners than in decliners (53%). Lung function and residual volume at baseline were higher in the declining group. Decliners presented with increased bronchial reactivity (ie, a lower provocative concentration of methacholine causing a 20% fall in FEV1) at baseline. Twenty-five percent of nondecliners were started on anti–interleukin-5 (anti–IL-5) for severe eosinophilic asthma during the study compared with 10% of decliners. The multivariable model suggested that Asthma Control Questionnaire score at baseline, late-onset asthma, and addition of anti–IL-5 during follow-up were associated with lower FEV1 decline, independently from other variables such as evolution in exacerbations, smoking status, inhaled corticosteroids or oral corticosteroids dose, or add-on anti–immunoglobulin E over time, whereas reversibility to salbutamol and higher FEV1 were associated with accelerated FEV1 decline. Conclusions: Add-on therapy with anti–IL-5 in severe eosinophilic asthma was associated with an attenuated FEV1 decline. The causality of this observation should, however, be confirmed in future prospective controlled studies.
AB - Background: Asthmatics have accelerated lung function decline over time compared with healthy individuals. Objective: To evaluate risk factors for accelerated lung function decline. Methods: In a longitudinal analysis on severe asthmatics enrolled in the Belgian Severe Asthma Registry with at least 2 visits a minimum of 12 months apart, we compared characteristics of patients with and without decline (loss of post-bronchodilation forced expiratory volume in 1 s [FEV1] (% predicted)/y greater than zero) over time. Multiple linear regression was applied to study the factors independently associated with FEV1 decline. Results: In the overall population (n = 318), median annual FEV1 decline was 0.27 (–4.22 to 3.80) % predicted/y over a period of 23 months (12–41 months). Asthma was less controlled at baseline in nondecliners than in decliners (53%). Lung function and residual volume at baseline were higher in the declining group. Decliners presented with increased bronchial reactivity (ie, a lower provocative concentration of methacholine causing a 20% fall in FEV1) at baseline. Twenty-five percent of nondecliners were started on anti–interleukin-5 (anti–IL-5) for severe eosinophilic asthma during the study compared with 10% of decliners. The multivariable model suggested that Asthma Control Questionnaire score at baseline, late-onset asthma, and addition of anti–IL-5 during follow-up were associated with lower FEV1 decline, independently from other variables such as evolution in exacerbations, smoking status, inhaled corticosteroids or oral corticosteroids dose, or add-on anti–immunoglobulin E over time, whereas reversibility to salbutamol and higher FEV1 were associated with accelerated FEV1 decline. Conclusions: Add-on therapy with anti–IL-5 in severe eosinophilic asthma was associated with an attenuated FEV1 decline. The causality of this observation should, however, be confirmed in future prospective controlled studies.
UR - http://www.scopus.com/inward/record.url?scp=85117137873&partnerID=8YFLogxK
U2 - 10.1016/j.jaip.2021.09.023
DO - 10.1016/j.jaip.2021.09.023
M3 - Article
VL - 10
SP - 467
EP - 477
JO - Journal of Allergy and Clinical Immunology: In Practice
JF - Journal of Allergy and Clinical Immunology: In Practice
SN - 2213-2198
IS - 2
ER -