Exploring the long-term utility of remotely monitored FeNO suppression testing in severe asthma

  • John Busby
  • , Joshua Holmes
  • , Mohammed Almutairi
  • , Irene Berrar-Torre
  • , Claire Butler
  • , Christabelle Chen
  • , Gráinne d'Ancona
  • , Paddy Dennison
  • , Sharron Gilbey
  • , David J Jackson
  • , Sumita Kerley
  • , Sukeshi Makhecha
  • , Adel Mansur
  • , Anna-Louise Nichols
  • , Pujan H. Patel
  • , Paul E. Pfeffer
  • , Hitasha Rupani
  • , Joan Sweeney
  • , Liam G. Heaney*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Background
Confirmation of optimal inhaled corticosteroid use is essential before initiating biologic therapy. Fractional exhaled nitric oxide (FeNO) suppression testing (FeNOSuppT) is a proven phenotyping technique; however, its long-term effect on clinical outcomes remains unclear.

Objectives
To assess the real-world feasibility of delivering FeNOSuppT alongside digital inhaler monitoring and to examine its effect on biologic initiation and clinical outcomes.

Methods
Prospective cohort study within 7 U.K. severe asthma centers. Patients received a sensor-enabled inhaled corticosteroid/long-acting β-agonist (ICS/LABA) inhaler during an initial appointment between July 2020 and June 2022. A positive FeNOSuppT was defined as greater than 42% FeNO reduction at short-term follow-up (typically 1–3 mo postbaseline). Biologic initiation and clinical outcomes were compared at short-term and long-term (typically 12 mo postbaseline) follow-up.

Results
Of 353 included patients, 257 (72.8%) completed the FeNOSuppT and 140 (54.5%) were positive. A positive FeNOSuppT was associated with greater improvements in the % predicted short-term forced expiratory volume in 1 second (FEV1%; 8.6% vs –0.3; P < .001) and the 6-Item Asthma Control Questionnaire (ACQ6; 0.7 vs 0.3; P = .001) compared with a negative test. Of 168 patients eligible for biologics who completed the FeNOSuppT, those with a positive result initiated biologics less often (48.2% vs 65.2%; P = .035). Despite this, there was a greater improvement in FEV1 (11.0% vs 2.3%; P = .016), and a similar reduction in both asthma symptoms (ACQ6 0.7 vs 0.8; P = .623) and exacerbations (66.7% vs 66.7%; P = .349) at long-term follow-up when compared with those with a negative FeNOSuppT.

Conclusions
Delivering FeNOSuppT aligned with digital monitoring is feasible within routine care. A positive FeNOSuppT was associated with lower rates of biologic initiation, with similar clinical outcomes.

Original languageEnglish
Pages (from-to)1816-1823
Number of pages8
JournalJournal of Allergy and Clinical Immunology: In Practice
Volume13
Issue number7
DOIs
Publication statusPublished - 07 Jul 2025

Keywords

  • adult
  • aged
  • female
  • humans
  • male
  • middle aged
  • administration, inhalation
  • adrenal cortex hormones/therapeutic use
  • anti-asthmatic agents/therapeutic use
  • asthma/drug therapy
  • fractional exhaled nitric oxide testing/methods
  • nitric oxide/analysis
  • prospective studies

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