The evidence of significant variability in lung function is required to confirm the clinical diagnosis of asthma. 1 This is commonly obtained in laboratory settings by bronchoreversibility or bronchoprovocation testing. Because the hallmark of asthma is the variability of symptoms, a more clinically relevant method to confirm the diagnosis should be by revealing an increase of spontaneous variability in lung function. 1 Studies using home measurements of peak expiratory flow (PEF) to monitor lung function consistently found a greater variability in asthmatic than healthy subjects, either within or between days, but with significant overlap between groups, which limits diagnostic accuracy. 2 Therefore, even if recommended by expert committees, 1 PEF is not commonly used in clinical practice. 3The forced oscillation technique (FOT) is an alternative lung function test conducted during quiet tidal breathing. In a pioneering study, Que et al 4 found that the variability of respiratory impedance measured by FOT over 15 minutes was significantly greater in asthmatics than healthy subjects. This finding, however, was not confirmed by other studies using similar short-term FOT monitoring. 5More recently, Gulotta et al 6 found the day-to-day variability of inspiratory resistance (CVR insp ) self-measured at home by FOT be significantly greater in asthmatic than healthy subjects when calculated over non-overlapped periods ≥4 consecutive days and averaged over 6 months. However, whether CVR insp identifies the presence of asthma in a clinical real-case scenario has not been reported yet. Therefore, we designed this prospective study to evaluate the predictive ability of FOT variability in identifying asthmatic subjects with mild intermittent asthma in comparison with the recommended assessment of PEF variability.Subjects with well-controlled mild intermittent asthma 1 and healthy controls were eligible for this study. The diagnosis of asthma was based on a detailed medical history and confirmed by airway hyperresponsiveness, that is, a provocative dose of methacholine causing a 20% decrease of FEV 1 <1000 μg. Exclusion criteria were smoking history >5 pack-years, obesity, diabetes, other respiratory diseases and current regular treatment with inhaled corticosteroids and/or long-acting beta-agonists. Healthy controls were non-smoker, non-obese subjects, without history of pulmonary disorders. The study was approved by the local Ethical Review Board (no. 50/2010), and all subjects gave written informed consent before the start of study.At inclusion, subjects had spirometry measured according to ATS-ERS standards and respiratory resistance by a FOT device (Resmon PRO DIARY, Restech Srl, Italy) identical to those used thereafter by each individual for home monitoring. 7 Subjects collected daily FOT data at 5 Hz in the morning for two consecutive weeks, without prior bronchodilator use. For performing FOT measurements, subjects were asked to breathe spontaneously for 2 minutes while connected to the device by a mouthpiece, seate...