Evidence map›Paper›PMID 42526931›Full record

ArticleBMJ open2026

Inhaled corticosteroids and risk of cardiovascular events in chronic obstructive pulmonary disease: a nationwide cohort study in Denmark.

Mia Ritzau Ishøj Nielsen, Emma Borremose Wedervang, Anna Kubel Vognsen, Karen Hougaard Frost, Alexander Ryder Jordan, Sigrid Anna Aalberg Vikjord, Alexander G Mathioudakis, Jens-Ulrik Stæhr Jensen, Pradeesh Sivapalan

Abstract read
In one paragraph

Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mia Ritzau Ishøj NielsenCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.ORCID 0009-0001-6776-5468
Emma Borremose WedervangCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.ORCID 0009-0005-7676-7069
Anna Kubel VognsenCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Karen Hougaard FrostCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.ORCID 0009-0008-4784-4696
Alexander Ryder JordanCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Sigrid Anna Aalberg VikjordDepartment of Pulmonary and Occupational Medicine, St. Olavs University Hospital, Trondheim, Norway.
Alexander G MathioudakisDivision of Immunology, Immunity to Infection and Respiratory Medicine, The University of Manchester School of Biological Sciences, Manchester, UK.ORCID 0000-0002-4675-9616
Jens-Ulrik Stæhr JensenCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Pradeesh SivapalanCopenhagen Respiratory Research, Department of Medicine, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark pradeesh.sivapalan.02@regionh.dk.ORCID 0000-0002-8620-3655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleCardiovascular disease is a major comorbidity in chronic obstructive pulmonary disease (COPD). Previous studies evaluating the association between inhaled corticosteroids (ICS) and cardiovascular events (CVEs) in COPD have yielded conflicting results and a potential dose-response relationship remains unclear.

objectivesTo determine the association between ICS exposure and risk of CVE in COPD patients.

methodsIn this nationwide, retrospective register-based cohort study, we included patients with a specialist-verified COPD diagnosis between January 2008 and January 2022. ICS exposure was quantified as mean daily budesonide-equivalent dose redeemed in the year prior to index and categorised as none, low (>0 µg/day and <400 µg/day), moderate (400-800 µg/day) or high (>800 µg/day). We assessed CVE risk using adjusted cause-specific Cox proportional hazards models, with additional sensitivity analyses including a complete-case analysis, time-varying Cox regression, Fine-Gray competing risk model, and a negative control outcome analysis.

resultsAmong 82 327 patients, 8948 (10.9 %) experienced a CVE during a 1-year follow-up. In the primary analysis, low- and moderate-dose ICS was associated with a significantly reduced CVE rate compared with no ICS use. A modest decrease in CVE rate was observed for moderate-dose ICS largely across all sensitivity analyses.

conclusionICS use in COPD was not associated with an increased risk of CVE at any dose level. A modest association with reduction in CVE risk was confined to moderate-dose ICS. These findings support the cardiovascular safety of ICS and reinforce that ICS prescribing should be guided by exacerbation risk and symptom burden rather than cardiovascular concern.

Indexed as

Adrenal Cortex HormonesCardiovascular DiseasesPulmonary Disease, Chronic ObstructiveAdministration, InhalationAgedDenmarkDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedProportional Hazards ModelsRegistriesRetrospective StudiesRisk FactorsAdrenal Cortex HormonesCardiovascular DiseaseChronic airways diseaseDrug TherapyPulmonary Disease

Identifiers

PMID42526931
PMCPMC13423070

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.