Evidence map›Paper›PMID 36300679›Full record

ArticleESC heart failure2023

Cabergoline treatment promotes myocardial recovery in peripartum cardiomyopathy.

Tobias J Pfeffer, Julia H Mueller, Lea Haebel, Sergej Erschow, Kuebra C Yalman, Steven R Talbot, Tobias Koenig, Dominik Berliner, Carolin Zwadlo, Michaela Scherr and 3 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  5. Pharmacological interventions for peripartum cardiomyopathy.The Cochrane database of systematic reviews · 2024
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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

13 authors at 2 institutions in 2 countries.

Tobias J PfefferDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Julia H MuellerDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Lea HaebelDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Sergej ErschowDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Kuebra C YalmanDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Steven R TalbotInstitute for Laboratory Animal Science and Central Animal Facility, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0002-9062-4065
Tobias KoenigDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Dominik BerlinerDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Carolin ZwadloDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Michaela ScherrDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Denise Hilfiker-KleinerDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0001-6065-9649
Johann BauersachsDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.
Melanie Ricke-HochDepartment of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0001-5479-2275
Medizinische Hochschule Hannover · DEPhilipps University of Marburg · DE

Funding

German Research Foundation HI 842/10-2German Research Foundation RI 2531/2-2Leducq Foundation 19CVD02Niedersächsische Ministerium für Wissenschaft und Kultur NiedersächsischesVorab-VWZN3452Niedersächsische Ministerium für Wissenschaft und Kultur REBIRTHI/II-ZN3440
6 · The paper itself

Abstract

aimsPeripartum cardiomyopathy (PPCM) is a rare heart disease, occurring in previously heart-healthy women during the last month of pregnancy or the first months after delivery due to left ventricular (LV) systolic dysfunction. A common pathomechanistic pathway of PPCM includes increased oxidative stress and the subsequent generation of a cleaved prolactin fragment (16 kDa PRL), which promotes the onset of heart failure (HF) in a microRNA (miR)-146a-dependent manner. Inhibition of prolactin secretion with the dopamine D2 receptor (D2R) agonist bromocriptine combined with standard HF therapy supports cardiac recovery. This study examined whether treatment with the more selective D2R agonist cabergoline prevents HF development in an experimental PPCM mouse model and might be used as an alternative treatment regime for PPCM. METHODS AND

resultsPostpartum (PP) female PPCM-prone mice with a cardiomyocyte restricted STAT3-deficiency (αMHC-Cre

conclusionsIn the experimental PPCM mouse model, the selective D2R agonist cabergoline prevents the onset of postpartum HF similar to bromocriptine. In PPCM patients, cabergoline treatment was safe and effective as all patients fully recovered. Cabergoline might serve as a promising alternative to bromocriptine. However, these findings are based on experimental data and a small case series and thus have to be interpreted with caution and should be validated in a larger clinical trial.

Indexed as

CardiomyopathiesHeart FailureMicroRNAsVentricular Dysfunction, LeftAnimalsBromocriptineCabergolineDopamine AgonistsFemaleMiceMyocytes, CardiacPeripartum PeriodPregnancyProlactinBromocriptineCabergolineDopamine AgonistsMicroRNAsProlactinBromocriptineCabergolineDopamine D2 receptor agonistHeart failurePeripartum cardiomyopathy (PPCM)

Identifiers

PMID36300679
PMCPMC9871652
OpenAlexW4307363596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.