Background Small airway dysfunction (SAD) is a key feature of severe asthma, contributing to poor symptom control and exacerbations. Tezepelumab has demonstrated efficacy in reducing exacerbations and improving lung function, but its specific effects on SAD remain underexplored. We aimed to assess changes in SAD among patients initiating Tezepelumab. Methods A prospective observational study among patients with severe asthma treated with Tezepelumab in a tertiary center. SAD was assessed at baseline and 6 months using impulse oscillometry (IOS) and spirometry. We focused on frequency dependence of resistance (R5–20) and the area under the reactance curve (AX) to define SAD, with pathologic cutoffs >0.1 kPa·L −1 ·s −1 and >1.0 kPa·L −1 , respectively. Paired analyses were used to compare changes over time. Results 34 patients were included (median age 60 years, 74% females, 21% biologic-experienced) with a median follow-up of 183 days. There were significant improvements from baseline to follow-up in FEV1 (median 1.73 versus 1.97 liters, p=0.001), MEF25–75 (median 1.26 versus 1.73 liter·s −1 , p=0.002), R5–20 (median 0.16 versus 0.08 kPa·L −1 ·s −1 , p<0.001) and AX (median 1.62 versus 0.80 kPa·L −1 , p<0.001). Improvements in IOS parameters were larger in patients with increased asthma control test scores ≥3 points. Prevalence of SAD decreased from 76% to 44% at follow-up (p=0.003). SAD at follow-up was associated with smoking, lower FEV1 and FVC, and smaller improvements in ACT score. Conclusion Tezepelumab significantly improved small airway function, which was associated with better asthma control. Our findings highlight SAD as a treatable trait in patients with severe asthma.
Kupershmidt et al. (Mon,) studied this question.