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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Atrial Fibrillation/Flutter in Transthyretin Cardiac Amyloidosis: Prevalence, Incidence, Clinical Predictors, and
Nicholas Chan1, Yevgeniy Brailovsky1, Sergio Teruya1
1Seymour, Paul and Gloria Milstein Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center and New York Presbyterian Hospital, New York, New York, USA; Clinical Cardiovascular Research Laboratory for the Elderly, New York, New York, USA.
Background:
Atrial fibrillation/flutter (AF) is common in transthyretin cardiac amyloidosis (ATTR-CA). The CHARGE-AF score has not been validated in ATTR-CA. The Columbia staging system is prognostic for survival, but its utility in predicting incident AF is unknown.
Objectives:
The authors aim to determine the predictors of prevalence and incidence of AF and the effect of tafamidis.
Methods:
This is a retrospective cohort study of 419 patients with ATTR-CA. AF was ascertained from review of electrocardiograms, extended rhythm, device interrogations, and charted history. Binary logistic regression assessed for factors associated with prevalent AF. Cox regression time-to-event analysis assessed for factors associated with incident AF.
Results:
AF was present in 58% (n = 244) of ATTR-CA at baseline. On multivariable logistic regression, higher Columbia score (OR: 1.48; 95% CI: 1.25-1.75) and higher left atrial volume index (LAVI) (OR: 1.05; 95% CI: 1.02-1.08) were associated with prevalent AF, whereas hereditary amyloid transthyretin (ATTRv) (OR: 0.19; 95% CI: 0.07-0.55) was protective (all P < 0.05). AF developed in 71 (41%) subjects without prior AF, over a median follow-up 2 years. On Cox regression, higher Columbia score (HR: 1.18; 95% CI: 1.01-1.38; P = 0.035) was associated with new onset AF, whereas CHARGE-AF and LAVI were not. ATTRv (HR: 0.44; 95% CI: 0.23-0.87; P = 0.017) and tafamidis (HR: 0.54; 95% CI: 0.30-0.95; P = 0.034) were protective.
Conclusions:
More than half of the ATTR-CA patients have AF, which was associated with wild-type amyloid transthyretin, greater Columbia stage, and increased LAVI. About half of the ATTR-CA individuals developed AF after 2 years, which was predicted by the Columbia score, but not the CHARGE-AF score. ATTRv and tafamidis were protective against incident AF.
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