Evidence map›Paper›PMID 40338121›Full record

ArticleClinical and translational allergy2025

Non-genetic factors associated with ACE-inhibitor and angiotensin receptor blocker-induced angioedema.

Diana Dubrall, Nora L Branding, Carina M Mathey, Anna M Weber, Michael Steffens, Maike Below, Matthias Schmid, Bettina Wedi, Dorothea Wieczorek, Philipp M Amann and 13 more

Abstract read
In one paragraph

Article in Clinical and translational allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Bradykinin-Mediated Angioedema Induced by Drugs.Journal of clinical medicine · 2025
    Review
  4. Article
  5. 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

23 authors.

Diana DubrallInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital of Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0002-8763-051X
Nora L BrandingResearch Division, Federal Institute of Drugs and Medical Devices (BfArM), Bonn, Germany.
Carina M MatheyResearch Division, Federal Institute of Drugs and Medical Devices (BfArM), Bonn, Germany.
Anna M WeberResearch Division, Federal Institute of Drugs and Medical Devices (BfArM), Bonn, Germany.
Michael SteffensResearch Division, Federal Institute of Drugs and Medical Devices (BfArM), Bonn, Germany.
Maike BelowCentral Research Institute for Ambulatory Health Care in Germany, Berlin, Germany.
Matthias SchmidInstitute for Medical Biometry, Informatics and Epidemiology, University Hospital of Bonn, Bonn, Germany.
Bettina WediKlinik für Dermatologie, Allergologie und Venerologie, Medizinische Hochschule Hannover, Hannover, Germany.
Dorothea WieczorekKlinik für Dermatologie, Allergologie und Venerologie, Medizinische Hochschule Hannover, Hannover, Germany.
Philipp M AmannKlinik für Dermatologie, Allergologie und Phlebologie, SLK-Kliniken Heilbronn, Heilbronn, Germany.
Harald LöfflerKlinik für Dermatologie, Allergologie und Phlebologie, SLK-Kliniken Heilbronn, Heilbronn, Germany.
Lukas KochDepartment of Dermatology and Venereology, Medical University of Graz, Graz, Austria.ORCID https://orcid.org/0000-0003-2091-5411
Clemens SchöfflDepartment of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
Heinrich DickelDepartment of Dermatology, Venereology and Allergology, St. Josef Hospital, University Medical Center, Ruhr University Bochum, Bochum, Germany.
Nomun GanjuurDepartment of Dermatology, Venereology and Allergology, St. Josef Hospital, University Medical Center, Ruhr University Bochum, Bochum, Germany.
Thorsten HornungZentrum für Hauterkrankungen, Universitätsklinikum Bonn, Bonn, Germany.
Timo BuhlKlinik für Dermatologie, Venerologie und Allergologie, Universitätsmedizin Göttingen, Göttingen, Germany.ORCID https://orcid.org/0000-0002-3139-129X
Emel Aygören-PürsünDepartment of Pediatrics, Goethe University Frankfurt, Frankfurt, Germany.
Gerda WurptsKlinik für Dermatologie und Allergologie - Hautklinik, Universitätsklinik der RWTH Aachen, Aachen, Germany.
Jens GreveDepartment of Otorhinolaryngology-Head and Neck Surgery, Ulm University Medical Center, Ulm, Germany.
Markus M NöthenInstitute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.
Andreas J ForstnerInstitute of Human Genetics, University of Bonn, School of Medicine and University Hospital Bonn, Bonn, Germany.
Bernhardt SachsResearch Division, Federal Institute of Drugs and Medical Devices (BfArM), Bonn, Germany.

Funding

Federal Insitute for Drugs and Medical Devices V-17454/68502/2017-2020Federal Insitute for Drugs and Medical Devices V-2020.2/68502/2020-2024Federal Insitute for Drugs and Medical Devices V2021.5/68502/2022-2024University Hospital Bonn V-17454/68502/2017-2020University Hospital Bonn V-2020.2/68502/2020-2024University Hospital Bonn V2021.5/68502/2022-2024
6 · The paper itself

Abstract

backgroundAngioedema (AE) rarely occurs as a potentially life-threatening adverse drug reaction (ADR) to angiotensin-converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB). The aim of the present study was to investigate non-genetic association factors with ACEi-/ARB-induced angioedema in the European ADR database EudraVigilance and the database of the vARIANCE study.

methodsThe cohort of the vARIANCE study comprised 114 patients who suffered from ACEi- or ARB-induced angioedema. In addition, 171 angioedema reports and 4650 reports on other ADRs of ACEi/ARB were identified in the ADR database EudraVigilance with the latter serving as a reference group. Odds ratios were calculated and a logistic regression analysis was performed using angioedema versus reference reports.

resultsIncreased age, smoking, allergies and a history of previous angioedema were identified as associated factors for ACEi-/ARB-induced angioedema. In most patients, the swelling affected the face, lips and tongue. In the vARIANCE study, about 70% of angioedema occurred after 1 year of treatment. For one in two patients in the vARIANCE study (84.2% with ACEi treatment) and one in three patients from the EudraVigilance reports (59.6% with ARB treatment), the angioedema resulted in hospitalization.

conclusionsWe found small to moderate associations with certain individual patient-related factors in this pharmaco-epidemiological study. As a future perspective, combining non-genetic association factors with corresponding genetic data might provide an option to compose stronger and individual risk scores.

Indexed as

angioedemaangiotensin‐converting enzyme inhibitorsangiotensin‐receptor blockersdrug‐induced angioedemaspontaneous reports

Identifiers

PMID40338121
PMCPMC12058302

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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.