# Atrial Fibrillation in Transthyretin Amyloid Cardiomyopathy: A Marker of Disease Severity but Not an Independent Predictor of Mortality

**Authors:** Carlos M Penate, Amalia Peix, Aylen Perez, Kenia Padron, Andrew S Dzebu, Carlos Fonseca, Jesus Rojas-Velazquez, Roxana Pazmino, Fernando Barba, Orlando Henriquez Italin

PMC · DOI: 10.7759/cureus.101917 · Cureus · 2026-01-20

## TL;DR

Atrial fibrillation is common in a heart disease called ATTR-CM but does not predict survival, instead reflecting more severe disease.

## Contribution

This study clarifies that atrial fibrillation marks disease severity but does not independently predict mortality in ATTR-CM patients.

## Key findings

- Atrial fibrillation was present in 50% of patients and linked to more advanced disease stages.
- Atrial fibrillation did not independently predict mortality after adjusting for disease stage and heart function.
- ATTR stage III was an independent predictor of mortality, highlighting its clinical importance.

## Abstract

Background and objective

Atrial fibrillation (AF) is the most common arrhythmia in patients with transthyretin amyloid cardiomyopathy (ATTR-CM), although its prognostic role remains uncertain. There is substantial evidence regarding mortality when AF coexists with heart failure (HF). However, this association is not well established in patients with ATTR-CM. This study aimed to assess whether AF was an independent predictor of all-cause mortality in ATTR-CM.

Methods

A total of 22 patients with confirmed ATTR-CM were followed (mean follow-up: 18.2 ± 6.8 months). The association between AF and all-cause mortality was evaluated using Cox proportional hazards modeling.

Results

The cohort had a mean age of 72 years (AF: 75.0 ± 5.5 years vs. no AF: 69.0 ± 8.7 years), and 81.8% of patients were men. Nine (41%) patients died during follow-up; among these, six (67%) had AF. AF was present in 11 (50%) of patients. AF was associated with more advanced disease, including a higher proportion of ATTR stage III (45.5% vs. 18.2%; p = 0.14) and New York Heart Association (NYHA) class III-IV symptoms (81.8% vs. 54.5%; p = 0.13). AF was not associated with all-cause mortality in the unadjusted analysis (hazard ratio (HR) 2.12; 95% confidence interval (CI): 0.53-8.52) or after adjustment for age, ATTR stage III vs. I-II, and left ventricular global longitudinal strain (LVGLS) > −15% (HR: 0.90; 95% CI: 0.12-6.98). In contrast, ATTR stage III vs. I-II remained an independent predictor of mortality (HR: 7.05; 95% CI: 1.55-31.98).

Conclusions

Patients with ATTR-CM carry a high mortality burden. AF is a common rhythm disorder in this population and appears to represent a more advanced disease phenotype rather than an independent predictor of all-cause mortality. These findings suggest that AF may function as a marker of disease progression and a valuable element for clinical stratification.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981), heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}
- **Diseases:** Dyspnea (MESH:D004417), hemodynamic impairment (MESH:D060825), chronic kidney disease (MESH:D051436), rhythm disorder (MESH:D021081), LVGLS (MESH:D018487), arrhythmia (MESH:D001145), LA (MESH:C535395), cardiomyopathy (MESH:D009202), stroke (MESH:D020521), CKD (MESH:D012080), AF (MESH:D001281), AV block (MESH:D054537), LA thrombus (MESH:D013927), Mortality (MESH:D003643), hypertension (MESH:D006973), III (MESH:C537189), ATTR stage III (MESH:D062706), ATTR-CM (MESH:C567782), CA (MESH:D000686), type 2 diabetes mellitus (MESH:D003924), light-chain (AL) amyloidosis (MESH:D000075363), HF (MESH:D006333), NYHA III (MESH:D006331), amyloid (MESH:C000718787)
- **Chemicals:** tafamidis (MESH:C547076), 99mTc-HMDP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12919734/full.md

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Source: https://tomesphere.com/paper/PMC12919734