Abstract

Deposition of amyloid in the heart can lead to cardiac dilation and impair its pumping ability. This ultimately leads to heart failure with worsening symptoms of breathlessness and fatigue due to the progressive loss of elasticity of the myocardium. Biomarkers linked to the clinical deterioration can be crucial in developing effective treatments. However, to date the progression of cardiac amyloidosis is poorly characterized. There is an urgent need to identify key predictors for disease progression and cardiac tissue function. In this proof of concept study, we estimate a group of new markers based on mathematical models of the left ventricle derived from routine clinical magnetic resonance imaging and follow-up scans from the National Amyloidosis Center at the Royal Free in London. Using mechanical modeling and statistical classification, we show that it is possible to predict disease progression. Our predictions agree with clinical assessments in a double-blind test in six out of the seven sample cases studied. Importantly, we find that multiple factors need to be used in the classification, which includes mechanical, geometrical and shape features. No single marker can yield reliable prediction given the complexity of the growth and remodeling process of diseased hearts undergoing high-dimensional shape changes. Our approach is promising in terms of clinical translation but the results presented should be interpreted with caution due to the small sample size.

Highlights

  • Amyloidosis occurs when proteins that take abnormal forms known as amyloid deposits build up in the tissues

  • cardiac magnetic resonance (CMR) Imaging The study consists of CMR images from seven cardiac amyloidosis patients before treatment and at 6 or 9 months after the treatment

  • To assess the mechanical features, below we analyze the mechanical response of the cardiac amyloidosis patients during the disease progression using our FE models with the inferred parameters

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Summary

Introduction

Amyloidosis occurs when proteins that take abnormal forms known as amyloid deposits build up in the tissues These deposits are composed of abnormal protein fibers that accumulate more quickly than they are cleared away, and interfere with the structure and function of affected organs throughout the body. These include the heart, liver, skin, lungs, kidneys, and nervous system (Gertz et al, 2013). When amyloid fibrils infiltrate in myocardium, the ventricles will show impaired contraction and relaxation. The AL type, can be life-threatening, the median survival of patients is half a year from the onset of heart failure (Grogan et al, 2017)

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