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Published on: July 20, 2022
The Prognostic and Diagnostic Role of Atrial Strain in Cardiomyopathies: A Literature Review
Beatrice Dal Passo1, Renè Tezze1, Federica Frascaro1
1Cardiology Unit, Azienda Ospedaliero-Universitaria S.Anna, Via Aldo Moro, Ferrara, Italy.
Insights
Atrial strain analysis using echocardiography and CMR is valuable for cardiomyopathies. It aids in differentiating phenotypes, predicting arrhythmias and adverse events, and monitoring treatment response.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Biomarkers
Background:
- Atrial strain assessment via speckle-tracking echocardiography and feature tracking cardiac magnetic resonance (CMR) is a valuable tool across various cardiomyopathies.
- Robust evidence exists for hypertrophic phenotypes, where left atrial strain (LAS) differentiates conditions like cardiac amyloidosis (CA), hypertrophic cardiomyopathy (HCM), Fabry cardiomyopathy (FD), and hypertensive heart disease.
Purpose of the Study:
- To evaluate the utility of atrial strain assessment in diagnosing and predicting outcomes in different cardiomyopathy phenotypes.
- To explore the prognostic value of LAS in hypertrophic and dilated cardiomyopathies and right atrial strain in arrhythmogenic right ventricular cardiomyopathy.
Main Methods:
- Utilized speckle-tracking echocardiography and feature tracking CMR for atrial strain assessment.
- Analyzed LAS in hypertrophic phenotypes (CA, HCM, FD, hypertensive heart disease) and dilated cardiomyopathies.
- Assessed right atrial strain in arrhythmogenic right ventricular cardiomyopathy.
Main Results:
- LAS values were lowest in CA compared to HCM, FD, and hypertensive heart disease.
- LAS predicts atrial arrhythmias (e.g., atrial fibrillation in CA and HCM) and major adverse cardiac events (MACE) in all phenotypes.
- Improvement in LAS was observed during disease-modifying therapy in HCM and FD.
- In dilated cardiomyopathies, LAS (primarily via CMR) predicts left ventricular reverse remodeling and MACE, differentiating from ischemic heart disease.
- Right atrial strain shows prognostic power for arrhythmic events in arrhythmogenic right ventricular cardiomyopathy, even before right atrial dilatation.
Conclusions:
- Atrial strain analysis is a versatile tool for characterizing cardiomyopathies, predicting clinical outcomes, and monitoring therapeutic effects.
- LAS is particularly useful in hypertrophic and dilated cardiomyopathies, while right atrial strain offers early prognostic insights in arrhythmogenic right ventricular cardiomyopathy.
Abstract:
Atrial strain assessment, both by speckle-tracking echocardiography and feature tracking cardiac magnetic resonance (CMR), represents a useful tool in all the spectrum of cardiomyopathies. The most robust evidence available in the literature concerns cardiomyopathies with a hypertrophic phenotype, in which left atrial strain (LAS) has demonstrated to be able to differentiate each phenotype, with cardiac amyloidosis (CA) having the lowest LAS values compared to hypertrophic cardiomyopathy (HCM), Fabry cardiomyopathy (FD), and hypertensive heart disease. LAS is also able to predict the occurrence of atrial arrhythmias, in particular atrial fibrillation in CA and HCM, and major adverse cardiac event (MACE) in all the phenotypes. Interestingly, both in HCM and FD, improvement in LAS values has been detected during disease-modifying therapy. In cardiomyopathies with a dilated phenotype as well, LAS, which has been more extensively evaluated through CMR compared to other cardiomyopathies, appears to have prognostic value with respect to left ventricular reverse remodeling and the occurrence of MACE and can help to differentiate dilated cardiomyopathy from ischemic heart disease with left ventricular dilatation. Finally, in arrhythmogenic right ventricular cardiomyopathy, right atrial strain has also demonstrated prognostic power, particularly for the occurrence of both atrial and ventricular arrhythmic events. Interestingly, impaired values of right atrial strain have been detected even in the absence of dilatation of the right atrium, suggesting an earlier involvement by fibro-fatty replacement and fibrosis.
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