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Updated: Jan 29, 2026

Morphological and Functional Assessment of the Right Ventricle Using 3D Echocardiography
Published on: October 28, 2020
Role of echocardiography in assessing cardiac amyloidoses: a systematic review
Jun Koyama1,2, Masatoshi Minamisawa3, Yoshiki Sekijima4
1Department of Internal Medicine, Maruko Central Hospital, Nakamaruko 1771-1, Ueda, Nagano, 386-0405, Japan. jkoyama@shinshu-u.ac.jp.
Insights
Echocardiography aids in diagnosing cardiac amyloidosis, a heart condition causing thickened left-ventricular walls. Advanced echocardiogram techniques show promise for predicting patient outcomes and improving cardiac function assessment.
Area of Science:
- Cardiology
- Medical Imaging
- Systemic Amyloidosis
Background:
- Cardiac amyloidosis involves increased left-ventricular (LV) wall thickness and often presents with diastolic dysfunction.
- Systemic amyloidoses can lead to congestive heart failure, with systolic dysfunction appearing in later stages.
- Echocardiography is a key noninvasive tool for evaluating cardiac structure and function in these patients.
Purpose of the Study:
- To review advancements in echocardiography for diagnosing and managing cardiac amyloidosis.
- To highlight the prognostic value of echocardiographic indices in systemic amyloidoses.
- To explore future echocardiographic techniques for improved cardiac assessment.
Main Methods:
- Review of current literature on echocardiography in cardiac amyloidosis.
- Analysis of echocardiographic indices for assessing LV morphology and function.
- Discussion of prognostic indicators, including LV longitudinal function and myocardial integrated backscatter.
Main Results:
- Echocardiography is effective for assessing cardiac morphology and function in cardiac amyloidosis.
- Specific echocardiographic indices demonstrate prognostic value for amyloidoses.
- LV longitudinal function and myocardial integrated backscatter variation appear to be strong predictors of adverse outcomes.
Conclusions:
- Echocardiography plays a crucial role in the diagnosis and management of cardiac amyloidosis.
- LV longitudinal function and myocardial integrated backscatter are significant prognostic markers.
- Emerging echocardiographic techniques, like automated interpretation, promise enhanced cardiac function and prognosis assessment.
Abstract:
Cardiac amyloidosis is a manifestation of one of several systemic amyloidoses, and is characterized by increased left-ventricular (LV) wall thickness and normal or decreased LV cavity size. Congestive heart failure in cardiac amyloidosis is characterized by a predominant diastolic LV dysfunction, and systolic dysfunction occurs only in late-stage disease. Echocardiography is a noninvasive, reproducible method for assessing cardiac morphology and function in cardiac amyloidosis, and some echocardiographic indices are prognostic for amyloidoses. This review describes the advances in echocardiography and its role in the diagnosis and management of cardiac amyloidoses. Our review suggests that LV longitudinal function and the cyclic variation of myocardial integrated backscatter may be the best predictors of adverse outcomes. In the future, new echocardiographic techniques, such as fully automated echocardiogram interpretation, should provide further useful information for assessing cardiac function and prognosis in cardiac amyloidosis patients.
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