# The diagnostic value of left atrial stiffness for heart failure with preserved ejection fraction in patients with paroxysmal atrial fibrillation

**Authors:** Jinzhi Lai, Xiaohan Qin, Dingding Zhang, Jiaqi Wang, Jiaqi Yu, Keyue Sun, Deyan Yang, Jingbo Fan, Lihua Zhang, Zhongwei Cheng, Kangan Cheng, Peng Gao, Hua Deng, Ligang Fang, Taibo Chen, Quan Fang, Yongtai Liu

PMC · DOI: 10.1186/s44156-026-00107-5 · Echo Research and Practice · 2026-02-23

## TL;DR

This study shows that measuring left atrial stiffness can help diagnose heart failure with preserved ejection fraction in patients with paroxysmal atrial fibrillation.

## Contribution

The study introduces left atrial stiffness as a novel diagnostic marker for HFpEF in paroxysmal AF patients.

## Key findings

- Left atrial stiffness combined with MVE’ provides high diagnostic accuracy for HFpEF in paroxysmal AF patients.
- The optimal cutoff value for the E/MVE’ to 3D LAEF ratio is 0.27 for distinguishing HFpEF cases.
- Combining LAS and MVE’ improves diagnostic efficiency compared to using either measure alone.

## Abstract

Left atrial (LA) function is impaired in both atrial fibrillation (AF) and heart failure with preserved ejection fraction (HFpEF). Diagnosing HFpEF remains challenging, especially in AF patients. This study aims to evaluate whether LA stiffness (LAS) can facilitate the diagnosis of HFpEF in patients with paroxysmal atrial fibrillation (pxAF).

A total of 187 pxAF patients were enrolled in the discovery cohort and underwent baseline transthoracic echocardiography (TTE). LAS was measured in all patients, and HFpEF was ascertained based on the H2FPEF score (44 high-probability of HFpEF [hp-HFpEF], 143 low-probability of HFpEF [lp-HFpEF]). The left ventricular diastolic function and LA function were significantly altered in the hp-HFpEF group compared to the lp-HFpEF group. Among all echocardiographic indices, the ratio of E/MVE’ to 3D LAEF as a surrogate of LAS showed the greatest diagnostic performance in distinguishing hp-HFpEF from lp-HFpEF in pxAF patients (AUC = 0.862, 95% CI 0.801–0.922, p < 0.001), with an optimal cutoff value of 0.27. Combining MVE’ and LAS revealed the highest diagnostic efficiency (LR + 12.18) compared to any single variable. The discriminatory value of LAS with MVE’ was further verified in the validation cohort with an LR + of 7.18.

LAS analyzed by conventional echocardiography combined with MVE’ is a non-invasive, decision-support approach for discriminating hp-HFpEF from lp-HFpEF in pxAF patients. The clinical trial registration number: ClinicalTrials.gov NCT05266144.

The online version contains supplementary material available at 10.1186/s44156-026-00107-5.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** chronotropic incompetence (MESH:D001022), myopathy (MESH:D009135), cardiomyopathy (MESH:D009202), atherosclerotic heart disease (MESH:D006331), hyperthyroidism (MESH:D006980), coronary artery disease (MESH:D003324), LA dysfunction (MESH:D018487), obese (MESH:D009765), tricuspid regurgitation (MESH:D014262), HF (MESH:D006333), structural (MESH:D020914), arrhythmia (MESH:D001145), endothelial (MESH:D005642), LA (MESH:D059446), HFpEF (MESH:D054144), impaired exercise capacity (MESH:D000092202), hypertension (MESH:D006973), LV hypertrophy (MESH:D017379), atrial stiffness (MESH:C566112), coronary atherosclerotic heart disease (MESH:D003327), LA dilation (MESH:C565277), inflammation (MESH:D007249), hyperlipidemia (MESH:D006949), atrial dysfunction (MESH:C538261), congenital heart disease (MESH:D006330), DM (MESH:D009223), dyspnea (MESH:D004417), impairment (MESH:D060825), stenosis or insufficiency (MESH:D000309), diabetes (MESH:D003920), Atrial fibrillation (MESH:D001281), valvular heart disease (MESH:D006349)
- **Chemicals:** N-terminal pro-brain natriuretic peptide (-)
- **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/PMC12927242/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927242/full.md

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Source: https://tomesphere.com/paper/PMC12927242