Evidence map›Paper›PMID 40790079›Full record

ArticleScientific reports2025

Assessment of the myocardial effects of Bradykinin inhibitors by cardiac magnetic resonance (CMR) in discharged COVID-19 patients.

Adriana Aparecida Bau, Roberto Schreiber, Eduarda O Z Minin, Luis Miguel da Silva, Layde Rosane Paim, Camila Nicolela Geraldo Martins, Andréa Coy-Canguçu, Maria Luiza Moretti, Marcelo Dantas Tavares de Melo, Sergio Dertkigil and 8 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–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

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

18 authors.

Adriana Aparecida Bau *Discipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Roberto Schreiber *Department of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Eduarda O Z MininDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Luis Miguel da SilvaDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Layde Rosane PaimDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Camila Nicolela Geraldo MartinsDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Andréa Coy-CanguçuDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Maria Luiza MorettiDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Marcelo Dantas Tavares de MeloFederal University of Paraiba, João Pessoa, Paraíba, Brazil.
Sergio DertkigilDepartment of Radiology, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Andrei SpositoDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Jose Roberto Matos-SouzaDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Wilson NadruzDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil.
Bruna BombassaroDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Eli MansourDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Lício A VellosoDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, São Paulo, Brazil.
Michael Jerosch-HeroldNon-Invasive Cardiovascular Imaging Program, Department of Radiology and Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Otávio Rizzi Coelho-FilhoDiscipline of Cardiology, School of Medical Science, Hospital das Clínicas, University of Campinas, UNICAMP, Rua Vital Brasil, 251-Cidade Universitária "Zeferino Vaz", Campinas, São Paulo, CEP:13083-888, Brasil. tavicocoelho@gmail.com.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303366/2015-0 and 406696/2021-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/15402-2, 2016/26209-1, and 2017/03708-5
6 · The paper itself

Abstract

Myocardial involvement associated with COVID-19 has been linked to worse clinical outcomes. In a recent study, both a bradykinin B2 receptor inhibitor (icatibant acetate) and plasma-derived C1 inhibitor (pdC1INH) led to an improvement in lung computed tomography scores and increased blood eosinophil counts. Nevertheless, the effects of these therapies on COVID-19-associated myocardial involvement remain uncertain. To evaluate the impact of bradykinin inhibitors on myocardial tissue abnormalities in patients with COVID-19. Survivors of COVID-19 treated with either icatibant or pdC1INH as a supplement to standard-care underwent cardiac magnetic resonance (CMR) myocardial tissue characterization with T1/T2 mapping and serum biomarker collection at 30 days and 6 months post-discharge. At 30 days post-discharge, left ventricular ejection fraction (LVEF) was normal across all groups (Standard-care: 62.6 ± 2.7%, pdC1INH: 64.9 ± 7.5%, icatibant: 66.7 ± 4.8%; p = 0.4), with no significant change at 6 months (p = 0.14). However, pdC1INH treatment significantly reduced myocardial T2 (p = 0.005) and intracellular water lifetime (τic) (p = 0.045), indicating reduced myocardial edema and cardiomyocyte hypertrophy. Anemia, affecting 63% of patients 30 days post-discharge, was associated with larger cardiomyocyte size and prolonged hospital stay (p < 0.001). Hemoglobin levels (11.92 ± 2.45 g/dL at discharge vs. 14.66 ± 1.36 g/dL at 6 months) were inversely linked to intracellular water lifetime (τ

Indexed as

BradykininBradykinin B2 Receptor AntagonistsCOVID-19COVID-19 Drug TreatmentHeartAgedFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMyocardiumPatient DischargeSARS-CoV-2BradykininBradykinin B2 Receptor Antagonistsicatibant

Identifiers

PMID40790079
PMCPMC12340153

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LicenceCC BY-NC-ND
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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.