Abstract
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed disease, resulting in heart failure, arrhythmias, and valvular disease in a sizable (but still undetermined) proportion of older patients. Disease modifying therapy exists but is more effective in earlier-stage disease. Effective screening methods are needed to identify ATTR-CM at a treatable stage and improve outcomes for this complex population.
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