Evidence map›Paper›PMID 42161424›Full record

ArticleOpen heart2026

Distribution of diffuse myocardial fibrosis is uneven and associated with left ventricular function in severe aortic stenosis.

Erica Holmberg, Jan Engvall, Eva Nylander, Hans Granfeldt, Éva Tamás

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Article in Open heart, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Erica HolmbergDepartment of Thoracic and Cardiovascular Surgery, Linkoping University Department of Health Medicine and Caring Sciences, Linköping, Sweden erica.holmberg@liu.se.ORCID http://orcid.org/0000-0002-2839-5839
Jan EngvallDepartment of Clinical Physiology, Linköping, Linkoping University Department of Health Medicine and Caring Sciences, Linköping, Sweden.
Eva NylanderDepartment of Clinical Physiology, Linköping, Linkoping University Department of Health Medicine and Caring Sciences, Linköping, Sweden.
Hans GranfeldtDepartment of Thoracic and Cardiovascular Surgery, Linkoping University Department of Health Medicine and Caring Sciences, Linköping, Sweden.
Éva TamásDepartment of Thoracic and Cardiovascular Surgery, Linkoping University Department of Health Medicine and Caring Sciences, Linköping, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAortic stenosis (AS) leads to left ventricular (LV) remodelling and fibrosis. Myocardial fibrosis can be focal and irreversible, associated with poor prognosis, or diffuse and potentially reversible after surgery. Cardiac magnetic resonance imaging (CMR) shows promise in quantifying diffuse myocardial fibrosis (DMF), but methods vary in precision. The aim of this study was to investigate the presence and distribution of DMF from myocardial biopsies and CMR tissue characteristics in severe AS. Secondarily, explore the association between DMF and LV function.

methodsForty-three patients with severe AS underwent CMR and transthoracic echocardiography within 1 week before surgical aortic valve replacement. CMR included balanced steady-state free-precession cine images, T1 relaxometry with Modified Look-Locker Inversion recovery and extracellular volume calculations. Endomyocardial biopsies were sampled.

resultsHistological analysis of 192 biopsies showed a median LV collagen volume fraction (CVF) of 19%, peaking in segment 1, according to the segment model recommended by the American Heart Association (AHA). There were significant moderate correlations between CVF and extracellular volume in AHA segments 1 (r² = 0.54, p<0.01) and 16 (r² = 0.44, p=0.03), where the DMF had the highest prevalence. Functional assessments demonstrated correlations between CVF and global circumferential and radial strain (r

conclusionCVF varied across LV segments and was significantly highest at the base of the heart, suggesting the start location for fibrosis. Systolic functional data correlated with CVF and T1 relaxation time.

Indexed as

Aortic Valve StenosisMagnetic Resonance Imaging, CineMyocardiumVentricular Function, LeftVentricular RemodelingAgedBiopsyEchocardiographyFemaleFibrosisGlobal Longitudinal StrainHumansMaleMiddle AgedSeverity of Illness IndexStroke VolumeAortic Valve StenosisEchocardiographyHeart FailureMagnetic Resonance Imaging

Identifiers

PMID42161424
PMCPMC13202011

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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.