Evidence map›Paper›PMID 41951797›Full record

ArticleBasic research in cardiology2026

Genetic background is associated with distinct patterns of proarrhythmogenic remodeling leading to atrial fibrillation in pigs with ischemic heart failure.

Zhihao Zhang, Julia Vlcek, Christina Heger, Valerie Pauly, Nora Hesse, Dominik Schüttler, Daphne Merkus, Eckhard Wolf, Ivica Medugorac, Stefan Kääb and 2 more

Abstract read
In one paragraph

Article in Basic research in cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Zhihao Zhang *Department of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Julia Vlcek *Department of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Christina HegerDepartment of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Valerie PaulyDepartment of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Nora HesseDepartment of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Dominik SchüttlerDepartment of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Daphne MerkusInterfaculty Center for Endocrine and Cardiovascular Disease Network Modelling and Clinical Transfer (ICONLMU), LMU Munich, Munich, Germany.
Eckhard WolfDZHK (German Centre for Cardiovascular Research), Partner Site Munich, Munich Heart Alliance (MHA), Munich, Germany.
Ivica MedugoracPopulation Genomics Group, Department of Veterinary Sciences, LMU Munich, 82152, Martinsried, Germany.
Stefan KääbDepartment of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Philipp Tomsits *Department of Medicine I, University Hospital, LMU Munich, Munich, Germany.
Sebastian Clauss *Department of Medicine I, University Hospital, LMU Munich, Munich, Germany. sebastian.clauss@med.uni-muenchen.de.ORCID 0000-0002-5675-6128

Funding

Chinese Government Scholarship CSC202006160016Corona-Stiftung S199/10079/2019Deutsche Forschungsgemeinschaft MA 2186/14-1Deutsche Stiftung für Herzforschung F/21/22Deutsches Zentrum für Herz-Kreislaufforschung 81X2600255Deutsches Zentrum für Herz-Kreislaufforschung 81Z0600206Deutsches Zentrum für Herz-Kreislaufforschung 81Z0600207Dutch Cardiovascular Alliance DCVA-2020B008-RECONNEXTERA-CVD 01KL1910
6 · The paper itself

Abstract

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia, driven by electrical and structural remodeling that promotes proarrhythmic substrates. Interindividual variability in susceptibility to remodeling triggers, such as myocardial ischemia, suggests the involvement of genetic determinants. Ischemic heart failure (IHF) was induced by a 90-min occlusion of the left anterior descending artery in pigs. After 30 days, animals underwent in vivo assessments, including right and left heart catheterization, electrocardiography, and electrophysiological studies, with AF inducibility tested by burst pacing. Atrial fibrosis was quantified using Masson's trichrome staining, and remodeling-associated gene expression was analyzed by quantitative PCR. Genetic background was assessed through single-nucleotide polymorphism (SNP) genotyping using the Porcine SNP60 BeadChip, with data analyzed against reference SNP datasets. Following myocardial infarction, all animals developed IHF with reduced ejection fraction and increased AF susceptibility. Overall, IHF was associated with enhanced atrial fibrosis, but a subset of animals displayed no fibrotic remodeling. Genetic analysis identified two groups of pigs with different genetic backgrounds within the cohort: a Pietrain-dominant and a Landrace-dominant background. Pietrain-dominant pigs developed significantly more atrial fibrosis, whereas Landrace-dominant pigs exhibited a pronounced shortening of the atrial effective refractory period. Differential regulation of fibrosis-associated genes, including FN, MMP2, TGFB, and JNK1, was observed between genetic backgrounds. These findings indicate that genetic background is associated with distinct patterns of atrial remodeling in response to IHF, influencing key determinants of AF susceptibility.

Indexed as

Atrial FibrillationAtrial RemodelingHeart FailureMyocardial IschemiaAnimalsDisease Models, AnimalFemaleFibrosisGenetic Predisposition to DiseasePhenotypePolymorphism, Single NucleotideSwineAtrial fibrillationFibrosisGeneticsIschemic heart failurePig modelProarrhythmic remodeling

Identifiers

PMID41951797
PMCPMC13186903

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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.