potential benefit from emerging therapies. 2 It has been reported that 13% of elderly patients (mean age, 82 years) who have heart failure with preserved ejection fraction (HFpEF) are diagnosed with ATTRwt. 3 Several postmortem studies found cardiac amyloid deposition in up to 25% of individuals over 80 years of age. 4 The precise diagnosis of CA requires endomyocardial biopsy (EMB) to demonstrate disease-specific deposition. However, EMB is a relatively invasive procedure 5 and so cannot be performed routinely, especially in elderly patients. A recent systematic evaluation of bone scintigraphy C ardiac amyloidosis (CA) is a secondary cardiomyopathy with a hypertrophic appearance caused by deposition of anomalous fibrillar proteins in the myocardial extracellular matrix that originated from a precursor-altered protein called amyloid. 1 There are 3 main types of CA: acquired monoclonal immunoglobulin light chain amyloidosis (AL amyloidosis); mutant transthyretin (TTR) amyloidosis (ATTRm); and wild-type transthyretin amyloidosis (ATTRwt). ATTRwt is becoming increasingly recognized because of aging of populations, advancements in the understanding of the disease's pathobiology, and the