SENS PubMed Publication Search
Wild-Type Transthyretin Cardiac Amyloidosis is Not Rare in Elderly Subjects: the CATCH Screening Study
Eur J Prev Cardiol. 2024 Mar 8:zwae093. doi: 10.1093/eurjpc/zwae093.
Alberto Aimo 1 2, Giuseppe Vergaro 1 2, Vincenzo Castiglione 1 2, Iacopo Fabiani 2, Andrea Barison 1 2, Francesco Gentile 1 2, Yu Fu Ferrari Chen 2, Assuero Giorgetti 2, Dario Genovesi 2, Gabriele Buda 3, Maria Franzini 4, Massimo Piepoli 5, Stefano Moscardini 6, Claudio Rapezzi 7 8, Marianna Fontana 9, Claudio Passino 1 2, Michele Emdin 1 2
Abstract:
Background: Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) affects older adults and is currently considered as a rare disorder.
Objective: We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population.
Methods: General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65-90 years, until 1,000 accepted. The following red flags were searched: interventricular septal thickness ≥12 mm, any echocardiographic, ECG or clinical hallmark of CA, or high sensitivity-troponin T ≥14 ng/L. Individuals with at least one red flag (n=346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted.
Results: Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (grade 3), left ventricular (LV) wall thickening, grade 2 to 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) >1,000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP <300 ng/L. The prevalence of ATTR-CA in subjects ≥65 years was calculated as 0.46% (i.e., 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2).
Conclusions: ATTRwt-CA is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease.
Objective: We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population.
Methods: General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65-90 years, until 1,000 accepted. The following red flags were searched: interventricular septal thickness ≥12 mm, any echocardiographic, ECG or clinical hallmark of CA, or high sensitivity-troponin T ≥14 ng/L. Individuals with at least one red flag (n=346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted.
Results: Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (grade 3), left ventricular (LV) wall thickening, grade 2 to 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) >1,000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP <300 ng/L. The prevalence of ATTR-CA in subjects ≥65 years was calculated as 0.46% (i.e., 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2).
Conclusions: ATTRwt-CA is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease.
PMID: 38456769
Tags: Disease prevalence, humans, TTR amyloidosis