Evidence map›Paper›PMID 41706389›Full record

ArticleThe international journal of cardiovascular imaging2026

Atrial fibrillation is linked to increased left ventricular fibrosis and inflammation measured by CMR with prognostic implications.

Julia M Treiber, J Sebastian Wolter, Sören J Backhaus, Luise von Haugwitz, Thomas Neumann, Malte Kuniss, Jörg Yogarajah, Valentina O Puentmann, Eike Nagel, Till Keller and 2 more

Abstract read
In one paragraph

Article in The international journal of cardiovascular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Julia M TreiberDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
J Sebastian WolterDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Sören J BackhausDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Luise von HaugwitzDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Thomas NeumannDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Malte KunissDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Jörg YogarajahDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Valentina O PuentmannInstitute of Experimental and Translational Cardiovascular Imaging, University Hospital Frankfurt, Frankfurt am Main, Germany.
Eike NagelInstitute of Experimental and Translational Cardiovascular Imaging, University Hospital Frankfurt, Frankfurt am Main, Germany.
Till KellerDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Samuel SossallaDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany.
Andreas RolfDepartment of Cardiology, Kerckhoff Heart Center, Bad Nauheim, Germany. a.rolf@kerckhoff-klinik.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately 30% of patients with atrial fibrillation (AF) develop heart failure (HF), but the underlying mechanisms and their impact on the left ventricle (LV) remain unclear. Fibrosis and inflammation are suspected contributors. This study aimed to investigate LV tissue characteristics in patients with and without AF using cardiac magnetic resonance imaging (CMR). Patients from a single-center CMR registry were categorized by AF status, adjudicated by two blinded investigators. LV fibrosis was assessed by native T1 and extracellular volume (ECV), while T2 indicated inflammation. Results were adjusted for LV ejection fraction (LVEF), end-systolic volume index (ESVi), and late gadolinium enhancement mass (LGEmass). Prognostic value was tested with multivariable Cox regression, using all-cause mortality or HF hospitalization at one year as the endpoint. Of 2,879 patients with one-year follow-up, 590 had AF. They showed lower LVEF and higher ESVi and LGEmass. After adjustment, AF was linked to higher T1 (p = 0.006), T2 (p = 0.01), and ECV (p < 0.001). Eighty-five patients reached the endpoint. In multivariable analysis, only T1 independently predicted outcome. Kaplan-Meier analysis showed patients with T1 above the median (1125 ms) had worse outcomes than those below, even without AF. The combination of AF and elevated T1 carried the poorest prognosis (p = 0.001). AF is closely associated with LV fibrosis and inflammation, with T1 emerging as an independent predictor of outcome. These findings suggest a mechanistic pathway with important prognostic implications. Prospective studies are warranted to confirm these associations and explore their role in patient stratification and management.

Indexed as

Atrial FibrillationInflammationMagnetic Resonance Imaging, CineMyocardiumVentricular Dysfunction, LeftVentricular Function, LeftVentricular RemodelingAgedFemaleFibrosisHeart FailureHumansKaplan-Meier EstimateMaleMiddle AgedMultivariate AnalysisAtrial fibrillationFibrosisInflammationLeft ventricular dysfunctionPrognosisT1-mapping

Identifiers

PMID41706389
PMCPMC13136204

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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.