
Systematic evaluation should be used to increase the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM), which is present in a significant number of heart failure (HF) with preserved ejection fraction (HFpEF) cases, according to a study published in JAMA Cardiology.
“HFpEF is common, is frequently associated with ventricular wall thickening, and has no effective therapy. ATTR-CM can cause the HFpEF clinical phenotype, has highly effective therapy, and is believed to be underrecognized,” the researchers wrote.
To examine the prevalence of ATTR-CM without and with systematic screening in patients with HFpEF and ventricular wall thickening, the researchers conducted a population-based cohort study of 1,235 consecutive patients with HFpEF both without, and with (n = 286) systematic screening. The population of interest were required to have a validated HF diagnosis, be 60 years of age or older, have an ejection fraction of 40% or greater, and a ventricular wall thickness of 12 mm or greater. The primary endpoints were defined as ATTR-CM prevalence by strategy (clinical diagnosis or systematic screening), age, and sex.