Evidence map›Paper›PMID 40823190›Full record

ArticleThe Lancet regional health. Europe2025

Cardiovascular safety of biologic therapies in patients with severe asthma: a nationwide cohort study in Belgium.

Frauke Van Vaerenbergh, Delphine Vauterin, Maxim Grymonprez, Lowie E G W Vanfleteren, Guy Brusselle, Lies Lahousse

Abstract read
In one paragraph

Article in The Lancet regional health. Europe, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. Kounis Syndrome Features in Special Populations.Medical sciences (Basel, Switzerland) · 2026
    Review
  3. Optimizing COPD Care in Belgium: A Multidisciplinary Expert Consensus on Cardiopulmonary Risk Management.International journal of chronic obstructive pulmonary disease · 2026
    Article
  4. From FEVJournal of asthma and allergy · 2026
    Review
  5. Review
  6. Article
  7. Article
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

6 authors.

Frauke Van VaerenberghDepartment of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent, 9000, Belgium.
Delphine VauterinDepartment of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent, 9000, Belgium.
Maxim GrymonprezDepartment of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent, 9000, Belgium.
Lowie E G W VanfleterenCOPD Center, Department of Respiratory Medicine and Allergology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Guy BrusselleDepartment of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
Lies LahousseDepartment of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent, 9000, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In last decades, biologic therapies have been approved for severe allergic and/or eosinophilic asthma. Limited studies have investigated the effect of biologics on (acute) cardiovascular events, which have reported conflicting results. We aimed to investigate the potential cardiovascular risk of anti-immunoglobulin(Ig)-E (omalizumab) and anti-interleukin(IL)-5/IL5 receptor (IL5R) therapies (mepolizumab and benralizumab) in patients with severe asthma compared with non-biologic users. Methods: Adult asthma patients eligible for biologics were identified in Belgian nationwide data between 2017 and 2022. Inverse probability of treatment weighted Cox regression was used to investigate cardiovascular outcomes and all-cause mortality, while controlling for age, sex, obesity, smoking, comorbidities, comedication, exacerbations, and frailty. Findings: This cohort study consisted of 171,865 patients (mean age 64 years; 55% females) including 1826 (1.1%) anti-IgE users and 2398 (1.4%) anti-IL5/IL5R users. Anti-IgE exposure was associated with a significantly lower risk of mortality (aHR 0.48, 95% CI 0.40-0.58), congestive heart failure (aHR 0.79, 95% CI 0.65-0.95), peripheral artery disease (aHR 0.66, 95% CI 0.51-0.86), and stroke (aHR 0.54, 95% CI 0.36-0.81). Anti-IL5/IL5R use was associated with a significantly lower risk of mortality (aHR 0.35, 95% CI 0.29-0.42), congestive heart failure (aHR 0.63, 95% CI 0.52-0.76), arrythmia (aHR 0.78, 95% CI 0.68-0.90), and peripheral artery disease (aHR 0.69, 95% CI 0.54-0.87) compared with non-biologic users. No significant differences in the risk of myocardial infarction and pulmonary embolism were observed. Interpretation: In this nationwide observational study, biologic therapies for patients with severe asthma were associated with a significantly lower risk of all-cause mortality and specific cardiovascular diseases compared with non-biologic users. Funding: None.

Indexed as

Anti-IgE therapyAnti-IL5 therapyAsthmaBiologicalCardiovascular eventsMonoclonal antibodyMortality

Identifiers

PMID40823190
PMCPMC12355080

What OpenQuestion holds

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Registered trials

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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.