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Use of High-Dose Inhaled Corticosteroids and Risk of Corticosteroid-Related Adverse Events in Asthma Findings From the NORDSTAR Cohort

  • Anna von Bülow*
  • , Susanne Hansen
  • , Patrik Sandin
  • , Alexandra Cooper
  • , Olivia Ernstsson
  • , Kirk Geale
  • , Lauri Lehtimäki
  • , Charlotte Ulrik
  • , Bernt Bøgvald Aarli
  • , Pinja Ilmarinen
  • , Sylvia Packham
  • , Ghada Hassan
  • , Asger Sverrild
  • , Helena Backman
  • , Jussi Karjalainen
  • , Vibeke Backer
  • , Alan Altraja
  • , Paula Kauppi
  • , Valentina Yasinska
  • , Maritta Kilpeläinen
  • Arja Viinanen, Johannes Martin-Schmid, Apostolos Bossios, Celeste Porsbjerg, Hannu Kankaanranta, Christer Janson
*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

30 Citations (Scopus)

Abstract

Background: The link between the use of oral corticosteroids (OCS) and adverse events (AEs) in asthma is well described. In contrast, whether the use of high-dose inhaled corticosteroids (ICS) poses a risk to these is unknown. Objective: To examine the association between ICS exposure and corticosteroid (CS)-related AEs. Methods: We conducted an observational cohort study using nationwide Swedish registry data from the NORdic Dataset for aSThmA Research (NORDSTAR) research collaboration. We included patients with asthma aged ≥18 years between 2009 and 2019 and calculated their current ICS exposure and average daily ICS dose (budesonide equivalent) in follow-up. The association between ICS exposure and CS-related AEs was analyzed using Cox proportional hazards models adjusting for age, sex, and OCS dose. Results: We included 529,203 patients with asthma. Overall, we observed increased hazard ratios (HRs) in those exposed to high-dose (≥800-1599 μg) and very high dose (≥1600 μg) ICS for several AEs, including cardiovascular disease, type 2 diabetes mellitus (T2DM), osteoporosis, and pneumonia compared with those not exposed to ICS. HRs for the current use of high-dose ICS ranged from 1.11 (95% confidence interval [CI]: 1.06-1.16) for T2DM to 1.65 (95% CI: 1.58-1.72) for pneumonia. Likewise, HRs linked to average daily high-dose ICS ranged from 1.16 (95% CI: 1.02-1.33) for pneumonia to 1.70 (95% CI: 1.38-2.08) for osteoporosis. Sensitivity analysis excluding patients using OCS showed that high-dose ICS was still associated with an increased risk of CS-related AEs. Overall, ICS <800 μg per day had no increased risk, except for cataract. Conclusion: High-dose ICS is associated with an increased risk of several CS-related AEs. This highlights the importance of clinicians considering this risk in patients treated with high-dose and very high dose ICS.

Original languageEnglish
Pages (from-to)1609-1619.e5
JournalJournal of Allergy and Clinical Immunology: In Practice
Volume13
Issue number7
DOIs
Publication statusPublished - 2025
Publication typeA1 Journal article-refereed

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adverse events
  • Asthma
  • Asthma management
  • Cardiovascular disease
  • Cataract
  • Inhaled corticosteroids
  • Oral corticosteroids
  • Osteoporosis
  • Severe asthma
  • Type 2 diabetes mellitus

Publication forum classification

  • Publication forum level 2

ASJC Scopus subject areas

  • Immunology and Allergy

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