Atrial fibrillation substrate and impaired left atrial function: a cardiac MRI study

心房颤动 心脏病学 内科学 医学 心功能曲线 心力衰竭
作者
Yaacoub Chahine,Nadia Chamoun,Ahmad Kassar,Lee Bockus,Fima Macheret,Nazem Akoum
出处
期刊:Europace [Oxford University Press]
卷期号:26 (11) 被引量:12
标识
DOI:10.1093/europace/euae258
摘要

Abstract Aims Structural and fibrotic remodelling is a well-known contributor to the atrial fibrillation (AF) substrate. Epicardial adipose tissue (EAT) is increasingly recognized as a contributor through electrical remodelling in the atria. We aimed to assess the association of LA fibrosis and EAT with LA strain and function using cardiac magnetic resonance (CMR) imaging in patients with AF. Methods and results LA fibrosis was assessed using late gadolinium enhancement CMR, LA EAT was assessed using the fat-water separation Dixon sequence, and feature tracking was applied to assess global longitudinal strain in its three components [reservoir (GLRS), conduit (GLCdS), and contractile (GLCtS)]. LA emptying fraction and LA volume were measured using the cine sequences. All CMR images were acquired in sinus rhythm. One hundred one AF patients underwent pre-ablation CMR (39% female, average age 62 years). LA fibrosis was negatively associated with the three components of global longitudinal strain (GLRS: R = −0.35, P < 0.001; GLCdS: R = −0.24, P = 0.015; GLCtS: R = −0.2, P = 0.046). Out of the different sections of the LA, fibrosis in the posterior and lateral walls was most negatively correlated with GLRS (R = −0.32, P = 0.001, and R = −0.33, P = 0.001, respectively). LA EAT was negatively correlated with GLCdS (R = −0.453, P < 0.001). LA fibrosis was negatively correlated with LA emptying fraction but LA EAT was not (R = −0.27, P = 0.007, and R = −0.22, P = 0.1, respectively). LA EAT and fibrosis were both positively correlated with LA volume (R = 0.38, P = 0.003, and R = 0.24, P = 0.016, respectively). Conclusion LA fibrosis, a major component of the AF substrate, and EAT, an important contributor, are associated with a worsening LA function through strain analysis by CMR.
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