Abstract

To assess left atrial (LA) function and determine the prevalence of LA dysfunction in AL amyloidosis (AL) using conventional and strain echocardiography. LA ejection fraction, LA filling fraction, LA ejection force, peak LA systolic strain rate (LAsSR), and LA systolic strain (LA epsilon) were determined in 95 AL patients (70 with and 25 without echocardiographic evidence of cardiac involvement, abbreviated CAL and NCAL, respectively), 30 age-matched controls (CON), and 20 patients with diastolic dysfunction and LA dilatation (DD). Peak LAsSR >2 standard deviations below mean CON value was used as the cut-off for normal LA function. LA ejection fraction was lower in CAL when compared with CON (40.4+/-13.6 vs. 67.0+/-6%, P=0.01). Left atrial septal strain rate and strain were lower in CAL (0.8+/-0.5 s(-1) and 5.5+/-4%, respectively) compared with CON (1.8+/-0.8 s(-1) and 14+/-4%, respectively, P=<0.0001), NCAL (1.6+/-0.8 s(-1) and 13+/-7%, respectively, P<0.0001) and DD (1.3+/-0.4 s(-1) and 10+/-2%, respectively, P<0.0001). Based on peak LA systolic strain rate criteria, the cut-off values for normal LA function were -1.1 s(-1) and -1.05 s(-1) for lateral and septal walls. Using these criteria, LA dysfunction was identified in 32% (lateral LA criteria) and 60% (septal LA criteria) of CAL patients. Lateral and septal LAsSR were lower in CAL patients with vs. those without symptoms of heart failure. Inter- and intra-observer agreement was high for LA strain echocardiography. LA function assessment using strain echocardiography is feasible with low intra- and inter-observer variability. LA dysfunction is observed in AL patients without other echocardiographic features of cardiac involvement and may contribute to cardiac symptoms in CAL.

Highlights

  • AL amyloidosis (AL; known as primary amyloidosis) is characterized by extracellular infiltration of various organs, including the heart, by fibrillar deposits derived from monoclonal light chain fragments.[1]

  • We evaluated Left atrial (LA) systolic function in AL amyloidosis patients using conventional and strain echocardiography

  • Echocardiographic features of cardiac involvement were present in 66 AL patients (CAL) and absent in 25 patients (NCAL)

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Summary

Introduction

AL amyloidosis (AL; known as primary amyloidosis) is characterized by extracellular infiltration of various organs, including the heart, by fibrillar deposits derived from monoclonal light chain fragments.[1] Clinical evidence of cardiac involvement occurs in 30–50% of AL patients and usually presents as diastolic dysfunction.[2] The left atrium modulates left ventricular (LV) filling through three components: an expansion component during ventricular systole, a conduit component during early ventricular diastole, and an active contractile component during late ventricular diastole. The active contractile component of the left atrium has an important role in patients with diastolic dysfunction, where the ‘atrial kick’ is critical to ventricular filling. AL amyloidosis is known to affect all cardiac chambers.[3] Left atrial (LA) involvement could potentially impair LA systolic function, which could further compromise ventricular filling and contribute to symptoms related to diastolic dysfunction.[4] We evaluated LA systolic function in AL amyloidosis patients using conventional and strain echocardiography

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