Abstract
Transthyretin and light-chain amyloidosis are the 2 main causes of cardiac amyloidosis. Recent developments in molecular imaging have transformed our ability to diagnose transthyretin cardiac amyloidosis noninvasively and unmasked a hitherto unrecognized prevalence of the disease. This review summarizes the current and evolving imaging approaches, their molecular structural basis, and the gaps in imaging capabilities that have arisen as a result of parallel developments in pharmacotherapy delivering the first effective treatment options for this condition.
Original language | English (US) |
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Pages (from-to) | 965-970 |
Number of pages | 6 |
Journal | Journal of Nuclear Medicine |
Volume | 61 |
Issue number | 7 |
DOIs | |
State | Published - Jul 1 2020 |
Keywords
- ATTR
- Bone-seeking tracers
- Cardiac amyloidosis
- Molecular imaging
- SPECT
ASJC Scopus subject areas
- General Medicine