Beyond conduction disease: a prospective screening study of transthyretin cardiac amyloidosis in older patients referred for device therapy after syncope
C Fumagalli, M Micillo, O Giuliano, F Scalone, R Marfella, G Limongelli, A Landolfi, C SarduAbstract
Background
Syncope in older adults is frequently attributed to bradyarrhythmias or conduction disease leading to cardiac implantable electronic device (CIED) implantation. However, transthyretin cardiac amyloidosis (ATTR-CM), an infiltrative cardiomyopathy associated with left ventricular hypertrophy (LVH), atrial fibrillation, heart failure, and progressive conduction system disease, may remain unrecognized in this setting. Data on ATTR-CM prevalence among older patients referred for CIED after syncope are limited.
Objective
To determine the prevalence of ATTR-CM in older patients referred for pacemaker or implantable cardioverter-defibrillator implantation after syncope and to evaluate the diagnostic yield of a pragmatic echocardiography-based screening strategy.
Methods
We conducted a prospective observational study including consecutive patients referred for CIED implantation following syncope over a 12-month period (01-12/2025). Device indication followed guideline-directed syncope and rhythm evaluation. Older age was defined as ≥70 years.
Screening for ATTR-CM was triggered by LVH (interventricular septum and/or posterior wall thickness ≥12 mm). In patients with LVH, the presence of ≥1 additional red flag (history suggestive of systemic amyloidosis and/or electrocardiographic low voltage or pseudo-infarct pattern) prompted further evaluation with bone-tracer scintigraphy and monoclonal protein assessment. ATTR-CM was diagnosed according to established criteria [1]. Genetic testing was performed after confirmation. Frailty was assessed using the Clinical Frailty Scale (CFS). Prevalence estimates are reported with 95% confidence intervals (CI).
Results
Among 457 patients evaluated for syncope, 85 were referred for CIED implantation (median age 78 [73–82] years; 61% male). Of these, 68/85 (80%) were aged ≥70 years.
LVH was present in 32/68 (47.1%) older patients. Among those with LVH, 14/32 (43.8%) had ≥1 additional red flag and underwent confirmatory testing. ATTR-CM was diagnosed in 4/14 patients (28.6%; 95% CI 8.4–58.1%). All cases were wild-type ATTR-CM (Figure).
Overall, prevalence of ATTR-CM among older individuals aged ≥70 years was 12.5% (95% CI 3.5–29.0). In ATTR-CM patients, device indication was mainly driven by atrial fibrillation–related bradyarrhythmia (3/4, 75%), while high-grade atrioventricular block accounted for 1/4 (25%). All ATTR-CM patients were frail (CFS ≥4).
Conclusions
Among older patients referred for CIED implantation after syncope, ATTR-CM was present in approximately 1 in 8 individuals with LVH. A simple echocardiography-driven screening strategy combining LVH with at least one additional red flag identified ATTR-CM in nearly one-third of tested patients.
These findings suggest that syncope and device referral pathways represent an important opportunity for early identification of ATTR-CM rather than solely a therapeutic endpoint for conduction disease.Figure