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In vivo quantification of amyloid burden in TTR-related cardiac amyloidosis.

Authors :
Kollikowski AM
Kahles F
Kintsler S
Hamada S
Reith S
Knüchel R
Röcken C
Mottaghy FM
Marx N
Burgmaier M
Source :
Intractable & rare diseases research [Intractable Rare Dis Res] 2017 Nov; Vol. 6 (4), pp. 291-294.
Publication Year :
2017

Abstract

Cardiac transthyretin-related (ATTR) amyloidosis is a severe cardiomyopathy for which therapeutic approaches are currently under development. Because non-invasive imaging techniques such as cardiac magnetic resonance imaging and echocardiography are non-specific, the diagnosis of ATTR amyloidosis is still based on myocardial biopsy. Thus, diagnosis of ATTR amyloidosis is difficult in patients refusing myocardial biopsy. Furthermore, myocardial biopsy does not allow 3D-mapping and quantification of myocardial ATTR amyloid. In this report we describe a <superscript>99m</superscript> Tc-DPD-based molecular imaging technique for non-invasive single-step diagnosis, three-dimensional mapping and semiquantification of cardiac ATTR amyloidosis in a patient with suspected amyloid heart disease who initially rejected myocardial biopsy. This report underlines the clinical value of SPECT-based nuclear medicine imaging to enable non-invasive diagnosis of cardiac ATTR amyloidosis, particularly in patients rejecting biopsy.

Details

Language :
English
ISSN :
2186-3644
Volume :
6
Issue :
4
Database :
MEDLINE
Journal :
Intractable & rare diseases research
Publication Type :
Academic Journal
Accession number :
29259858
Full Text :
https://doi.org/10.5582/irdr.2017.01065