Diagnostic and prognostic value of the left atrial myopathy evaluation in cardiac amyloidosis using echocardiography

Author:

Ferkh Aaisha12,Geenty Paul12,Stefani Luke12,Emerson Peter12,Pham Jennifer2,Byth Karen3,Boyd Anita C.4,Richards David4,Taylor Mark S.5,Kwok Fiona6,Kizana Eddy127,Thomas Liza128

Affiliation:

1. Westmead Clinical School University of Sydney Westmead New South Wales Australia

2. Department of Cardiology Westmead Hospital Westmead New South Wales Australia

3. WSLHD Research and Education Network Westmead Hospital Westmead New South Wales Australia

4. Westmead Private Cardiology Westmead New South Wales Australia

5. Department of Clinical Immunology and Allergy Westmead Hospital Westmead New South Wales Australia

6. Department of Haematology Westmead Hospital Westmead New South Wales Australia

7. Centre for Heart Research The Westmead Institute for Medical Research Westmead New South Wales Australia

8. South‐West Clinical School University of New South Wales Liverpool New South Wales Australia

Abstract

AbstractBackgroundCardiac amyloidosis (CA) is an under‐recognized cause of heart failure. Left atrial (LA) myopathy contributes to a worse prognosis in heart failure and is a feature of transthyretin (ATTR) and light‐chain (AL) CA. LA mechanical dispersion (LA‐MD) is a novel marker of intra‐atrial dyssynchrony implicated in LA myopathy and the future development of atrial fibrillation (AF).AimsThis study aimed to determine the characteristics and prognostic value of LA myopathy in ATTR and AL cardiomyopathy through a comprehensive LA echocardiographic evaluation.MethodsATTR (n = 86) and AL (n = 86) CA patients were compared with hypertensive heart disease (HHT) patients (n = 58). Transthoracic echocardiographic measurements including LA strain and LA‐MD were obtained with patient follow‐up for mortality.ResultsATTR and AL patients had a median follow‐up of 66 months, with 26 mortality events. Left ventricular (LV) mass, diastolic function (average‐e′ and E/e′), LV global longitudinal strain, and LA volume and function (LA function index and strain) were more impaired in ATTR versus AL; these echocardiographic parameters were more impaired in both amyloid groups compared to HHT patients (P < 0.05). LA‐MD was increased in ATTR versus AL [median 72.2 (inter‐quartile range 55–88.9) vs. 54 (43.5–64.2), respectively, P < 0.001]. Multivariable logistic regression adjusted for age, presence of AF, LV mass, global and basal strain, and E/e′ demonstrated that LA‐MD was an independent determinant of ATTR CA (P = 0.014). On multivariable analysis, LA reservoir strain was independently associated with the presence of heart failure in the CA group (P < 0.001). LA minimum volume (cut‐off ≥18 mL/m2) was a determinant of mortality in AL CA [Cox proportional hazard ratio (HR) 1.042 (1.003–1.082), P = 0.034 and Kaplan–Meier analysis, P = 0.016].ConclusionCharacterizing LA myopathy has significant diagnostic and prognostic utility in CA. ATTR patients have increased atrial dyssynchrony, which may have implications for AF development. LA reservoir strain was associated with heart failure in CA, whilst LA minimum volume was a predictor of mortality in AL CA.

Publisher

Wiley

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