Nuclear Medicine Techniques in the Diagnosis of Cardiac Amyloidosis

Cardiac amyloidosis (CA) represents the accumulation and deposition of misfolded protein fibrils in the myocardium, resulting in progressive restrictive cardiomyopathy. Light chain (AL) and transthyretin (TTR) amyloidosis are the most common types of CA. While endomyocardial biopsy remains the gold standard for diagnosing cardiac amyloidosis, its invasive nature and associated risk of complications have led to increased reliance on clinical suspicion and noninvasive imaging modalities as alternative diagnostic tools. Over the last decade, radionuclide imaging studies have become a widely accepted tool in diagnosing ATTR CA, whereas its diagnostic utility in AL CA detection remains limited. Recent advances in PET-CT radiopharmaceuticals have further expanded the potential of nuclear imaging as a comprehensive tool for diagnosis, prognostication, and therapy monitoring. This literature review appraises the current applications of nuclear imaging in the clinical management of cardiac amyloidosis.