# Sleep-disordered breathing in patients with heart failure with preserved left ventricular ejection fraction

**Authors:** Cornelia Grimm, Christian Viniol, Mikail Degerli, Olaf Hildebrandt, Karl Kesper, Ulrich Koehler, Wolfram Grimm, Mariana Parahuleva

PMC · DOI: 10.1007/s11325-026-03635-w · Sleep & Breathing = Schlaf & Atmung · 2026-03-13

## TL;DR

This study finds that sleep-disordered breathing is common in patients with heart failure and preserved ejection fraction, with distinct differences between obstructive and central sleep apnea.

## Contribution

The study provides new insights into the prevalence and clinical predictors of sleep-disordered breathing in heart failure patients with preserved ejection fraction.

## Key findings

- Sleep-disordered breathing was found in 42% of patients with heart failure and preserved ejection fraction.
- Obstructive sleep apnea was more common than central sleep apnea in this patient group.
- Obstructive sleep apnea was associated with higher BMI, while central sleep apnea was linked to more severe heart failure indicators.

## Abstract

Data on sleep-disordered breathing (SDB) in patients with heart failure with preserved left ventricular ejection fraction (HFpEF) are sparse. Therefore, we aimed to determine the prevalence and characteristics of SDB in a large patient cohort with HFpEF.

A total of 233 patients with HFpEF were prospectively enrolled at our cardiology outpatient department after excluding patients with a history of SDB. The presence of moderate to severe SDB with an apnea-hypopnea index ≥ 15/h was determined using cardiorespiratory polygraphy. All patients underwent assessment of HFpEF comorbidities, comprehensive echocardiographic studies, NT-proBNP levels and calculation of HFpEF-scores.

SDB was found in 97 of 233 patients (42%) with predominantly obstructive sleep apnea (OSA) in 64 patients (27%) and predominantly central sleep apnea (CSA) in 33 patients (14%). Male sex, body mass index, NYHA heart failure class III, NT-proBNP levels, HFpEF scores, chronic kidney disease, coronary artery disease, left ventricular (LV) mass index and E/E’ ratio by echocardiography were significant predictors of SDB by univariate analysis. Patients with predominantly CSA were significantly older and had higher NT-proBNP levels and a higher NYHA heart failure class than patients with OSA. Patients with OSA had a significantly higher body mass index (BMI) and a higher Epworth Sleepiness score. Multivariate analysis revealed male gender, BMI and LV mass index as significant predictors for OSA, whereas CSA was associated with a higher HFA-PEFF score and male gender.

Moderate to severe SDB is a frequent comorbidity in patients with HFpEF. Predominantly OSA is more frequent than CSA with significant clinical differences between patients with OSA compared to CSA. Whereas OSA is associated with a higher BMI in addition to male gender, CSA is associated with more advanced heart failure as indicated by higher HFA-PEFF scores, NYHA heart failure class and NT-proBNP levels.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252), sleep-disordered breathing (MONDO:0005296), obstructive sleep apnea (MONDO:0007147), central sleep apnea (MONDO:0004731), chronic kidney disease (MONDO:0005300), coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}
- **Diseases:** HFpEF (MESH:D054144), CSA (MESH:D020182), oxygen desaturation (MESH:D000860), obesity (MESH:D009765), Renal Disease (MESH:D007674), Excessive daytime sleepiness (MESH:D006970), atrial fibrillation (MESH:D001281), Apnea (MESH:D001049), tricuspid regurgitation (MESH:D014262), SDB (MESH:D012891), chronic kidney disease (MESH:D051436), AHI (MESH:D020181), coronary artery disease (MESH:D003324), diastolic dysfunction (MESH:D018487), hypertension (MESH:D006973), aortic valve stenosis (MESH:D001024), heart failure (MESH:D006333), daytime sleepiness (MESH:D012893)
- **Chemicals:** oxygen (MESH:D010100), creatinine (MESH:D003404), N-terminal pro-brain natriuretic peptide (-), natriuretic peptide (MESH:D045265)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12987792