Potential Cardiac Amyloid PET/CT Imaging Targets for Differentiating Immunoglobulin Light Chain From Transthyretin Amyloidosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11886-021-01506-2.pdf
Reference24 articles.
1. Ruberg FL, Grogan M, Hanna M, Kelly JW, Maurer MS. Transthyretin amyloid cardiomyopathy: JACC state-of-the-art review. J Am Coll Cardiol. 2019;73:2872–91 This review provides a thorough review on the pathophysiology, clinical manifestation, outcome, and treatment of cardiac TTR amyloidois.
2. Falk RH, Comenzo RL, Skinner M. The systemic amyloidoses. N Engl J Med. 1997;337:898–9.
3. Chen W, Dilsizian V. Molecular imaging of amyloid deposits for early diagnosis of cardiac amyloidosis and monitoring treatment response. JACC Cardiovasc Imaging. 2020;13(6):1348–52.
4. Gillmore JD, Maurer MS, Falk RH, Merlini G, Damy T, Dispenzieri A, et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis. Circulation. 2016;133:2404–12.
5. Zhang KW, Stockerl-Goldstein KE, Lenihan DJ. Emerging therapeutics for the treatment of light chain and transthyretin amyloidosis. JACC Basic Transl Sci. 2019;4:438–48 Excellent review on present and evolving treatment options in cardiac amyloidosis.
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3. Quantitative SPECT/CT Parameters in the Assessment of Transthyretin Cardiac Amyloidosis—A New Dimension of Molecular Imaging;Journal of Cardiovascular Development and Disease;2023-05-31
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