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Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Epicardial fat and atrial fibrillation: the perils of atrial failure
Andrea Lorenzo Poggi1, Bénédicte Gaborit2,3, Thomas Hellmut Schindler4
1Department of Internal Medicine, First Clinic of Internal Medicine, University of Genoa, 6 viale Benedetto XV, 16132 Genoa, Italy.
Insights
Obesity and epicardial adipose tissue (EAT) dysfunction promote atrial remodeling and increase atrial fibrillation (AF) risk. Weight loss and cardiovascular drugs may mitigate EAT dysfunction, reducing AF onset and recurrence.
Area of Science:
- Cardiology
- Metabolic Syndrome
- Electrophysiology
Background:
- Obesity, particularly epicardial adipose tissue (EAT) accumulation, is linked to cardiovascular disease, including atrial fibrillation (AF).
- Epicardial adipose tissue (EAT) dysfunction contributes to atrial remodeling through paracrine signaling, inflammation, and fibrosis, independent of mechanical stretch.
- Atrial fibrillation (AF) is now understood as the endpoint of atrial remodeling, involving structural, electrical, and autonomic nervous system changes.
Purpose of the Study:
- To elucidate the role of dysfunctional epicardial adipose tissue (EAT) in orchestrating left atrial (LA) remodeling.
- To update the understanding of the pathophysiological link between EAT dysfunction and AF.
- To review the potential benefits of weight loss and cardiovascular drugs on EAT dysfunction, LA remodeling, and AF.
Main Methods:
- Review of current literature on EAT, LA remodeling, and AF pathophysiology.
- Analysis of the pro-inflammatory and pro-fibrotic secretome of dysfunctional EAT.
- Examination of structural and cellular changes in the atrium due to EAT dysfunction.
Main Results:
- Dysfunctional EAT releases inflammatory and fibrotic factors, altering the atrial microenvironment.
- EAT dysfunction induces structural changes (fibro-fatty infiltration) and cellular alterations (mitochondrial uncoupling, sarcoplasmic reticulum fragmentation).
- These changes lead to electrical remodeling and autonomic nervous system involvement, promoting AF.
Conclusions:
- Dysfunctional EAT is a key driver of LA remodeling and AF development.
- Understanding EAT's role provides new insights into AF pathophysiology and treatment strategies.
- Weight loss and specific cardiovascular drugs show potential in managing EAT dysfunction and reducing AF burden.
Abstract:
Obesity is a heterogeneous condition, characterized by different phenotypes and for which the classical assessment with body mass index may underestimate the real impact on cardiovascular (CV) disease burden. An epidemiological link between obesity and atrial fibrillation (AF) has been clearly demonstrated and becomes even more tight when ectopic (i.e. epicardial) fat deposition is considered. Due to anatomical and functional features, a tight paracrine cross-talk exists between epicardial adipose tissue (EAT) and myocardium, including the left atrium (LA). Alongside-and even without-mechanical atrial stretch, the dysfunctional EAT may determine a pro-inflammatory environment in the surrounding myocardial tissue. This evidence has provided a new intriguing pathophysiological link with AF, which in turn is no longer considered a single entity but rather the final stage of atrial remodelling. This maladaptive process would indeed include structural, electric, and autonomic derangement that ultimately leads to overt disease. Here, we update how dysfunctional EAT would orchestrate LA remodelling. Maladaptive changes sustained by dysfunctional EAT are driven by a pro-inflammatory and pro-fibrotic secretome that alters the sinoatrial microenvironment. Structural (e.g. fibro-fatty infiltration) and cellular (e.g. mitochondrial uncoupling, sarcoplasmic reticulum fragmentation, and cellular protein quantity/localization) changes then determine an electrophysiological remodelling that also involves the autonomic nervous system. Finally, we summarize how EAT dysfunction may fit with the standard guidelines for AF. Lastly, we focus on the potential benefit of weight loss and different classes of CV drugs on EAT dysfunction, LA remodelling, and ultimately AF onset and recurrence.
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