# Prognostic implications of right ventricular to pulmonary artery uncoupling in cardiac amyloidosis

**Authors:** Aiste Monika Jakstaite, Anja Hänselmann, Samira Soltani, Eleonora Angelini, Michael Heuser, Vega Gödecke, Stefan Gingele, Thomas Skripuletz, Johann Bauersachs, Udo Bavendiek, Dominik Berliner

PMC · DOI: 10.3389/fcvm.2025.1653950 · Frontiers in Cardiovascular Medicine · 2025-09-29

## TL;DR

This study shows that poor right ventricular-pulmonary artery coupling is linked to higher mortality in patients with cardiac amyloidosis.

## Contribution

The study evaluates multiple echocardiographic surrogates of RV–PA coupling and their prognostic value in cardiac amyloidosis.

## Key findings

- Lower RV–PA coupling surrogates were independently associated with higher mortality in cardiac amyloidosis patients.
- TAPSE/PASP showed the strongest prognostic discrimination for predicting long-term survival.
- RV–PA uncoupling may indicate a higher risk of all-cause mortality in both ATTR-CA and AL-CA patients.

## Abstract

Right ventricular–pulmonary arterial (RV–PA) uncoupling in cardiac amyloidosis (CA) has been underexplored, with focus mainly on tricuspid annular plane systolic excursion (TAPSE)/pulmonary artery systolic pressure (PASP). This study aims to evaluate the association of various echocardiographic surrogates of RV–PA coupling with outcomes in cardiac transthyretin (ATTR-CA) and light-chain (AL-CA) amyloidosis.

We analyzed RV–PA coupling in patients diagnosed with ATTR-CA and AL-CA at our center between 2014 and 2023. RV–PA coupling was assessed using TAPSE/PASP, fractional area change (FAC)/PASP, and RV free wall strain (RVFWS)/PASP. The primary endpoint was all-cause mortality.

A total of 120 patients (86% ATTR-CA, 14% AL-CA) were included in the study (median age 77 years, 88% male). During a median follow-up period of 23 (IQR: 15–34) months, the primary endpoint occurred in 25 patients (21%). The study population was stratified based on the ROC-derived TAPSE/PASP cutoff of <0.30 mm/mmHg, demonstrating RV–PA uncoupling. Lower RV–PA coupling surrogates were independently associated with higher mortality (HR per +0.1 unit: TAPSE/PASP, 0.74, 95% CI: 0.59–0.93, p = 0.011; FAC/PASP, 0.87, 0.77–0.98, p = 0.018; RVFWS/PASP, 0.78, 0.63–0.97, p = 0.024). TAPSE/PASP demonstrated the strongest prognostic discrimination (AUC: 0.79, bootstrapped 95% CI: 0.66–0.91), compared with FAC/PASP (AUC: 0.75, 0.58–0.91) and RVFWS/PASP (AUC: 0.72, 0.52–0.87).

RV–PA uncoupling may be linked to a higher risk of all-cause mortality in CA. TAPSE/PASP outperformed numerically FAC/PASP and RVFWS/PASP in predicting long-term survival, although it did not clearly outperform established RV function parameters.

## Linked entities

- **Diseases:** light-chain amyloidosis (MONDO:0019438)

## Full-text entities

- **Genes:** TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}
- **Diseases:** light-chain (AL-CA) amyloidosis (MESH:D000075363), ATTR-CA (MESH:D000686)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12515962/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12515962/full.md

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Source: https://tomesphere.com/paper/PMC12515962