Evidence map›Paper›PMID 36882221›Full record

ArticleBMJ open respiratory research2023

Renin-angiotensin-system inhibitors and the risk of exacerbations in chronic obstructive pulmonary disease: a nationwide registry study.

Frida Vilstrup, Christian Kjer Heerfordt, Peter Kamstrup, Caroline Hedsund, Tor Biering-Sørensen, Rikke Sørensen, Shailesh Kolekar, Ole Hilberg, Lars Pedersen, Thomas Kromann Lund and 5 more

Abstract read
In one paragraph

Article in BMJ open respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

15 authors.

Frida VilstrupDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.
Christian Kjer HeerfordtDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.ORCID 0000-0001-8485-3235
Peter KamstrupDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.ORCID 0000-0002-5499-7171
Caroline HedsundDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.
Tor Biering-SørensenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Kobenhavn, Denmark.
Rikke SørensenDepartment of Cardiology, Copenhagen University Hospital, Kobenhavn, Denmark.
Shailesh KolekarDepartment of Clinical Medicine, University of Copenhagen, Kobenhavn, Denmark.
Ole HilbergDepartment of Medicine, Sygehus Lillebalt Vejle Sygehus, Vejle, Denmark.
Lars PedersenDepartment of Respiratory Medicine and Infectious Diseases, Bispebjerg Hospital, Copenhagen, Denmark.
Thomas Kromann LundSection for Lung Transplantation, Dept. of Cardiology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Tobias Wirenfeldt KlausenDepartment of Medicine, Section of Respiratory Medicine, Herlev Hospital, Herlev, Denmark.
Kristoffer Grundtvig SkaarupDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte Hospital, Hellerup, Denmark.
Josefin EklöfDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.
Pradeesh SivapalanDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark.
Jens-Ulrik Stæhr JensenDepartment of Medicine, Section of Respiratory Medicine, Gentofte University Hospital, Hellerup, Denmark jens.ulrik.jensen@regionh.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe renin-angiotensin system (RAS) has been shown to play a role in the pathogenesis of chronic obstructive pulmonary disease (COPD) because of the inflammatory properties of the system. Many patients with COPD use RAS-inhibiting (RASi) treatment. The aim was to determine the association between treatment with RASi and the risk of acute exacerbations and mortality in patients with severe COPD.

methodsActive comparator analysis by propensity-score matching. Data were collected in Danish national registries, containing complete information on health data, prescriptions, hospital admissions and outpatient clinic visits. Patients with COPD (n=38 862) were matched by propensity score on known predictors of the outcome. One group was exposed to RASi treatment (cases) and the other was exposed to bendroflumethiazide as an active comparator in the primary analysis.

resultsThe use of RASi was associated with a reduced risk of exacerbations or death in the active comparator analysis at 12 months follow-up (HR 0.86, 95% CI 0.78 to 0.95). Similar results were evident in a sensitivity analysis of the propensity-score-matched population (HR 0.89, 95% CI 0.83 to 0.94) and in an adjusted Cox proportional hazards model (HR 0.93, 95% CI 0.89 to 0.98).

conclusionIn the current study, we found that the use of RASi treatment was associated with a consistently lower risk of acute exacerbations and death in patients with COPD. Explanations to these findings include real effect, uncontrolled biases, and-less likely-chance findings.

Indexed as

Pulmonary Disease, Chronic ObstructiveReninAngiotensinsBendroflumethiazideEnzyme InhibitorsHumansRegistriesAngiotensinsBendroflumethiazideEnzyme InhibitorsReninCOPD epidemiologyCOPD ExacerbationsCOPD PathologyCOPD Pharmacology

Identifiers

PMID36882221
PMCPMC10008458

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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.