Prevalence of transthyretin cardiac amyloidosis in patients with heart failure with preserved ejection fraction: the PRACTICA study

Transthyretin cardiac amyloidosis (ATTR-CA) is a frequent cause of heart failure with preserved ejection fraction (HFpEF). This study sought to determine the prevalence of ATTR-CA among HFpEF patients in a multicenter nationwide study. Consecutive ambulatory or hospitalized patients aged ≥ 50 years with HFpEF and left ventricle hypertrophy ≥ 12mm were studied at 20 Spanish hospitals. Screening for cardiac amyloidosis was initiated according to the usual clinical practice of each center. Positive scintigraphs were centrally analyzed. 422 patients were included, of whom 387 underwent further screening for cardiac amyloidosis. A total of 65 patients (16.8%) were diagnosed with ATTR-CA, none below 75 years. There was an increase of prevalence with age. Of them, 60% were male, with a mean age of 85.3±5.2 years, mean left ventricle ejection fraction of 60.3±7.6% and a mean maximum left ventricle wall thickness of 17.2 [12-25] mm. Most of the patients were New York Heart Association class II (48.4%) or III (46.8%). Besides being older than non-ATTR-CA patients, ATTR-CA patients had higher median NT-proBNP levels (3801 [2266-7132] vs 2391 [1141-4796] pg/mL; P=.003). There was no statistical difference in the prevalence of ATTR-CA by sex (19.7% for men and 13.8% for women, P=.085). A ∼7% (4/56) of the patients exhibited a genetic variant (ATTRv). This multicenter nationwide study found a prevalence of 16.8%, confirming that ATTR-CA is a significant contributor to HFpEF in male and female patients with left ventricle hypertrophy and more than 75 years. La amiloidosis cardiaca por transtirretina (ATTR-AC) es una causa frecuente de insuficiencia cardiaca con fracción de eyección conservada (IC-FEc). El objetivo de este estudio fue determinar la prevalencia de ATTR-AC en pacientes con IC-FEc en un estudio multicéntrico a nivel nacional. Se estudiaron pacientes consecutivos ambulatorios u hospitalizados ≥ 50 años con IC-FEc e hipertrofia ventricular izquierda ≥ 12mm en 20 hospitales españoles. Se inicio cribado de amiloidosis cardiaca según práctica clínica habitual de cada centro; las gammagrafías positivas se analizaron centralmente. Se incluyeron 422 pacientes, 387 de los cuales evaluados para amiloidosis cardiaca. Un total de 65 pacientes (16,8%) se diagnosticaron de ATTR-AC, ninguno