The fraction of exhaled nitric oxide (F ENO ) is a biomarker for type 2 asthma, reflecting the degree of local pulmonary inflammation linked to immune pathways, including interleukin (IL)-13 [1]. In clinical practice, F ENO is a reliable marker for inhaled corticosteroid (ICS) responsiveness [2] and the efficacy of biological therapies, such as those targeting IL-4/IL-13 pathways [3, 4], as well as the detection of steroid nonadherence or resistance in severe asthma [2]. The prospective Severe Asthma Registry of the German Asthma Net (GAN) enrols patients with severe asthma for in-depth assessment of phenotypes, underlying mechanisms and therapeutic strategies; GAN has been approved by respective ethics committees, with all included patients having signed informed consent [5]. Prior studies of F ENO either included patients with asthma of any severity [6] or did not involve a comprehensive analysis in a large cohort [7]. We therefore used cross-sectional data from GAN to determine the correlation of F ENO with epidemiological, laboratory, clinical, lung function, or quality of life parameters and the need for oral corticosteroid (OCS) maintenance therapy in a carefully selected severe asthma cohort to better characterise the severe asthma subtype with high F ENO values.At the time of data acquisition (October 2019), GAN included 1689 patients with severe asthma, as defined by the European Respiratory Society/American Thoracic Society [1], from multiple tertiary referral centres, mainly in Germany, but also in Slovenia, Austria and Croatia [5]. F ENO was measured using any available device, according to the manufacturer's instructions [8]. Patients were included in the analysis if a F ENO measurement was available and excluded only if essential data were missing. Consistent with German and international guidelines [1, 9], F ENO values ⩾25 ppb were considered elevated; exacerbations were defined as events requiring OCS for ⩾3 days, doubling of established OCS dose, or hospitalisation; and thresholds for lung function parameters and exacerbation frequency were established. Controlled asthma was defined by Asthma Control Questionnaire-5 (ACQ-5) score <1.5, or Asthma Control Test (ACT) score ⩾20, with better asthma quality of life defined by mini Asthma Quality of Life Questionnaire (mAQLQ) score ⩾5.4 [1, 9]. Hypoxaemia was defined as partial pressure of oxygen in the blood (P O 2 ) <72 mmHg, and obesity as body mass index (BMI) ⩾30 kg•m −2 . Total IgE cut-off was aligned with the German criteria for anti-IgE therapy of 75 U•mL −1 [9]. Information bias was addressed by requiring an online form to be completed on assessment of the patient. The study was approved by the ethics committee of the Medical University of Vienna (EK 1849/2019), as well as by further local committees as per local requirements. Since the registry was initiated as a longitudinal project, data acquisition was not selective or biased towards any hypotheses. The significance level for hypothesis testing was set to 0.05. Due to the exploratory charac...