Published in:
Open Access
01-09-2019 | Magnetic Resonance Imaging | Cardiac PET, CT, and MRI (P Schoenhagen, Section Editor)
Cardiac Amyloidosis: Updates in Imaging
Authors:
Liza Chacko, Raffaele Martone, Francesco Cappelli, Marianna Fontana
Published in:
Current Cardiology Reports
|
Issue 9/2019
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Abstract
Purpose of Review
We summarize key features pertaining to the two most commonly encountered types of cardiac amyloidosis (CA), monoclonal immunoglobulin light chain (AL) and transthyretin type (ATTR), expanding upon the clinical application and utility of various imaging techniques in diagnosing CA.
Recent Findings
Advances in imaging have led to earlier identification, improved diagnosis of CA and higher discriminatory power to differentiate CA from other hypertrophic phenocopies. The application of cardiac magnetic resonance imaging (CMR) has led to a deeper understanding of underlying pathophysiological processes in CA, owing largely to its intrinsic tissue characterization properties. The widespread adoption of bone scintigraphy algorithms has reduced the need for cardiac biopsy and improved diagnostic confidence in ATTR CA.
Summary
As new treatments for CA are rapidly developing, there will be even greater reliance on imaging, as the requirement to diagnose disease earlier, monitor response and amend treatment strategies accordingly intensifies.