Abstract
Cardiac amyloidosis, once considered untreatable, is now gaining well-deserved attention due to advances in imaging and the recent approval of targeted breakthrough therapies. In this paper, we discuss the role of radionuclide imaging in the evaluation and management of patients with the most common form of amyloidosis—cardiac transthyretin amyloidosis (ATTR). We provide a comprehensive summary of the literature interspersed with our institutional experience as appropriate, to deliver our perspective.
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Disclosures
Dr. Singh has no disclosures. Dr. Falk has research grants from Ionnis, Alnylam, Glaxo Smith Kline and Pfizer. He serves as a consultant for Proclara. Dr. Di Carli has research grant from Spectrum Dynamics and Gilead, and consulting fees from Sanofi and GE. Dr. Dorbala served as a consultant with Advanced Accelerator Applications, General Electric and Proclara. Dr. Rapezzi has research grants from Pfizer and consulting fees from Pfizer and Alnylam.
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Dr. Dorbala is supported by NIH RO1 Grant (RO1 HL 130563) and the American Heart Association Grant (AHA 16 CSA 2888 0004). Dr. Falk is supported by NIH RO1 Grant (RO1 HL 130563).
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Singh, V., Falk, R., Di Carli, M.F. et al. State-of-the-art radionuclide imaging in cardiac transthyretin amyloidosis. J. Nucl. Cardiol. 26, 158–173 (2019). https://doi.org/10.1007/s12350-018-01552-4
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DOI: https://doi.org/10.1007/s12350-018-01552-4