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Transthyretin Amyloid Cardiomyopathy: Current Diagnostic Approach and Risk Stratification with Multimodality Imaging.
Georgios Tziomalos1, Thomas Zegkos1, Eleftheria Baltagianni1
1Department of Cardiology, AHEPA Hospital, School of Medicine, Aristotle University of Thessaloniki, 54636 Thessaloniki, Greece.
Timely diagnosis of transthyretin amyloid cardiomyopathy using multimodality cardiac imaging is crucial. Imaging biomarkers aid in risk stratification and assessing treatment response for improved patient outcomes.
Area of Science:
- Cardiology
- Medical Imaging
- Biomarkers
Background:
- Amyloidosis is an infiltrative disease potentially causing cardiomyopathy.
- Transthyretin amyloid cardiomyopathy requires timely and accurate diagnosis for effective treatment.
Purpose of the Study:
- To review the role of multimodality cardiac imaging in transthyretin amyloid cardiomyopathy.
- To discuss imaging's application from diagnosis to prognosis and treatment response.
Main Methods:
- Review of multimodality imaging techniques including ECG, echocardiography, cardiac MRI, and bone scintigraphy.
- Analysis of imaging biomarkers for disease assessment and risk stratification.
Main Results:
- Multimodality imaging raises suspicion and bone scintigraphy aids diagnosis, often obviating biopsy.
- Cardiac imaging biomarkers provide prognostic insights at diagnosis and after treatment.
Conclusions:
- Multimodality cardiac imaging is vital for managing transthyretin amyloid cardiomyopathy.
- Imaging facilitates personalized patient care by tracking disease evolution and treatment efficacy.
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