Atrial fibrosis heterogeneity is a risk for atrial fibrillation in pigs with ischaemic heart failure

Author:

Zhang Zhihao123,Vlcek Julia13,Pauly Valerie123,Hesse Nora123,Bauer Julia123,Chataut Kavi Raj123,Maderspacher Florian123,Volz Lina Sophie123,Buchberger Katharina123,Xia Ruibing123,Hildebrand Bianca1,Kääb Stefan124,Schüttler Dominik123,Tomsits Philipp123,Clauss Sebastian1234ORCID

Affiliation:

1. Department of Medicine I, Campus Grosshadern University Hospital Munich, Ludwig‐Maximilians University (LMU) Munich Germany

2. German Center for Cardiovascular Research (DZHK) Partner Site Munich, Munich Heart Alliance Munich Germany

3. Institute of Surgical Research at the Walter‐Brendel‐Centre of Experimental Medicine University Hospital, LMU Munich Munich Germany

4. Interfaculty Center for Endocrine and Cardiovascular Disease Network Modelling and Clinical Transfer (ICONLMU) LMU Munich Munich Germany

Abstract

AbstractBackgroundAtrial fibrillation (AF) is the most common arrhythmia and is associated with considerable morbidity and mortality. Ischaemic heart failure (IHF) remains one of the most common causes of AF in clinical practice. However, ischaemia‐mediated mechanisms leading to AF are still incompletely understood, and thus, current treatment approaches are limited. To improve our understanding of the pathophysiology, we studied a porcine IHF model.MethodsIn pigs, IHF was induced by balloon occlusion of the left anterior descending artery for 90 min. After 30 days of reperfusion, invasive haemodynamic measurements and electrophysiological studies were performed. Masson trichrome and immunofluorescence staining were conducted to assess interstitial fibrosis and myofibroblast activation in different heart regions.ResultsAfter 30 days of reperfusion, heart failure with significantly reduced ejection fraction (left anterior obique 30°, 34.78 ± 3.29% [IHF] vs. 62.03 ± 2.36% [control], p < .001; anterior–posterior 0°, 29.16 ± 3.61% vs. 59.54 ± 1.09%, p < .01) was observed. These pigs showed a significantly higher susceptibility to AF (33.90% [IHF] vs. 12.98% [control], p < .05). Histological assessment revealed aggravated fibrosis in atrial appendages but not in atrial free walls in IHF pigs (11.13 ± 1.44% vs. 5.99 ± .86%, p < .01 [LAA], 8.28 ± .56% vs. 6.01 ± .35%, p < .01 [RAA]), which was paralleled by enhanced myofibroblast activation (12.09 ± .65% vs. 9.00 ± .94%, p < .05 [LAA], 14.37 ± .60% vs. 10.30 ± 1.41%, p < .05 [RAA]). Correlation analysis indicated that not fibrosis per se but its cross‐regional heterogeneous distribution across the left atrium was associated with AF susceptibility (r = .6344, p < .01).ConclusionOur results suggest that left atrial cross‐regional fibrosis difference rather than overall fibrosis level is associated with IHF‐related AF susceptibility, presumably by establishing local conduction disturbances and heterogeneity.

Funder

China Scholarship Council

Deutsche Forschungsgemeinschaft

Deutsches Zentrum für Herz-Kreislaufforschung

European Research Area Network on Cardiovascular Diseases

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

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