Evidence map›Paper›PMID 41894223›Full record

ArticleEuropace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology2026

Association of non-invasive atrial cardiomyopathy markers with cerebral stroke lesions: a population-based analysis from the Hamburg City Health Study.

Marie Biedermann, Lena Koch, Silvia Becker, Ana Bošnjak, Amir S Jadidi, Dirk Westermann, Heiko Lehrmann, Thomas Arentz, Axel Loewe, Bastian Cheng and 6 more

Abstract read
In one paragraph

Article in Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

16 authors.

Marie BiedermannDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.
Lena KochDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0009-0007-4399-7794
Silvia BeckerDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0000-0002-1135-6446
Ana BošnjakDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0009-0003-9628-0931
Amir S JadidiDepartment of Cardiology, Heart Center Lucerne-Lucerne Cantonal Hospital, Lucerne, Switzerland.ORCID 0000-0002-6402-2845
Dirk WestermannDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0000-0002-7542-1956
Heiko LehrmannDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0000-0003-2377-1417
Thomas ArentzDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0009-0007-8115-0703
Axel LoeweInstitute of Biomedical Engineering, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.ORCID 0000-0002-2487-4744
Bastian ChengDepartment of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-2434-1822
Götz ThomallaDepartment of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Helge KniepDepartment of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-5258-2370
Jens FiehlerDepartment of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-8533-7478
Daniel EnglerDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-9519-6258
Renate B SchnabelDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-7170-9509
Martin EichenlaubDepartment of Cardiology and Angiology, Medical Center, Faculty of Medicine, University of Freiburg, Suedring 15, Bad Krozingen 79189, Germany.ORCID 0000-0003-3674-790X

Funding

AmgenBayerDeutsche Gesetzliche UnfallversicherungDeutsches KrebsforschungszentrumDeutsche Stiftung für HerzforschungDeutsches Zentrum für Herz-Kreislauf-ForschungFoundation Leducq 16 CVD 03German Research Foundation 529821741German Research Foundation LO 2093/11-1HCHSJoachim Herz FoundationKühne Foundation 116074Leibniz ScienceCampusNovartisSchillerSeefried StiftungSiemensTopconUnileverUniversity Medical Center Hamburg-Eppendorf 825903University Medical Center Hamburg-Eppendorf H2020
6 · The paper itself

Abstract

aimsAtrial fibrillation (AF) is a well-known risk factor for ischaemic stroke. Emerging evidence suggests that atrial cardiomyopathy (AtCM), independent of AF, may be a key contributor to stroke risk. We aimed to evaluate whether non-invasive AtCM markers assessed by electrocardiography (ECG), transthoracic echocardiography (TTE), and blood-based biomarkers provide incremental diagnostic value beyond established clinical risk factors for identifying cerebral stroke lesions on magnetic resonance imaging (MRI). METHODS AND

resultsWe analysed 1794 Hamburg City Health Study participants who underwent cerebral MRI with available baseline 12-lead ECG and TTE in sinus rhythm. Logistic regression analyses were performed to identify associations between non-invasive AtCM markers and stroke lesions. The incremental discriminatory performance of these markers beyond clinical risk factors was assessed. Stroke lesions were present in 152 participants (8.5%). Male sex, history of prior AF, and higher CHA2DS2-VA score were significantly associated with stroke lesions. Among AtCM markers, amplified P-wave duration (APWD), P-wave area in lead II, PR interval, left atrial volume index, left atrial ejection fraction, and NT-proBNP were also significant. Combining both clinical and AtCM markers, only CHA2DS2-VA score (OR: 1.95 per point, 95% CI: 1.49-2.55, P < 0.001) and P-wave area in lead II (OR: 0.99 per 100 µV·ms, 95% CI: 0.98-1.00, P = 0.031) remained independent predictors. However, this resulted in only marginal improvement in discrimination (ΔAUC: 0.03, 95% CI: 0.0001-0.0594) compared with the clinical risk factor model alone.

conclusionThe incremental diagnostic value of AtCM markers beyond clinical risk factors for MRI-defined cerebral lesions is limited, likely reflecting the heterogeneous aetiology of stroke lesions in a general population cohort.

Indexed as

Atrial FibrillationCardiomyopathiesStrokeAgedBiomarkersEchocardiographyElectrocardiographyFemaleGermanyHumansLogistic ModelsMagnetic Resonance ImagingMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Atrial fibrillationBiomarkersECGNon-invasive screeningStrokeTTE

Identifiers

PMID41894223
PMCPMC13122356

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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.