# Electrocardiographic Alterations in Obstructive Sleep Apnea Syndrome: Mechanisms and Clinical Relevance

**Authors:** Andrea Segreti, Michele Pelullo, Virginia Ligorio, Aurora Ferro, Riccardo Cricco, Martina Ciancio, Simone Pasquale Crispino, Francesco Grigioni

PMC · DOI: 10.3390/life16020251 · 2026-02-02

## TL;DR

This paper reviews how obstructive sleep apnea affects heart rhythms and how ECG changes can help detect and manage the condition.

## Contribution

The paper synthesizes current knowledge on ECG manifestations of OSA and highlights emerging AI and wearable technologies for detection.

## Key findings

- OSA is linked to ECG abnormalities like arrhythmias and repolarization changes.
- Daytime ECG markers may indicate subclinical cardiac remodeling and autonomic imbalance.
- AI and wearable ECG monitoring are emerging tools for OSA detection and risk assessment.

## Abstract

Obstructive Sleep Apnea (OSA) is a highly prevalent yet frequently underdiagnosed disorder strongly associated with cardiovascular morbidity and mortality. It is characterized by recurrent episodes of intermittent hypoxia, intrathoracic pressure swings, and sleep fragmentation that trigger sympathetic hyperactivation, oxidative stress, systemic inflammation, and progressive structural cardiac remodeling. These mechanisms translate into a wide range of electrocardiographic (ECG) abnormalities, including both nocturnal brady- and tachyarrhythmias, as well as daytime conduction and repolarization changes. This narrative review synthesizes current knowledge on ECG manifestations of OSA, encompassing atrial and ventricular ECG characteristics and the burden of supraventricular and ventricular arrhythmias. Emerging evidence suggests that several daytime ECG markers may represent accessible, low-cost indicators of subclinical cardiac remodeling and autonomic imbalance, with potential clinical implications. In addition, there is a rapidly evolving landscape of artificial intelligence applications and wearable-based ECG monitoring for OSA detection and risk stratification. Standardization of ECG-derived markers, validation across diverse populations, and integration into clinical workflows represent key priorities for future research. Recognizing ECG alterations associated with OSA may support earlier diagnosis, improved arrhythmic risk stratification, and more effective multidisciplinary management.

## Linked entities

- **Diseases:** Obstructive Sleep Apnea (MONDO:0007147)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, GJA1 (gap junction protein alpha 1) [NCBI Gene 2697] {aka AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** PSVCs (MESH:D018880), arrhythmic (OMIM:212500), PVCs (MESH:D018879), airway obstruction (MESH:D000402), CIH (MESH:D000860), bradyarrhythmia (MESH:D001919), brady- and tachyarrhythmias (MESH:D013610), arrhythmia (MESH:D001145), LV dysfunction (MESH:D018487), respiratory disorder (MESH:D012131), sudden cardiac death (MESH:D016757), hypercapnia (MESH:D006935), stroke (MESH:D020521), sleep-related disease (MESH:D020183), myocardial injury (MESH:D009202), anterior fascicular block (MESH:D002037), endothelial dysfunction (MESH:D014652), VF (MESH:C537182), AD (MESH:D000544), abnormalities of ventricular repolarization (MESH:D018754), asystole (MESH:D006323), Ventricular loading abnormalities (MESH:C536761), fibrosis (MESH:D005355), Inflammatory (MESH:D007249), atrial disease (MESH:D004194), cardiomyocyte injury (MESH:D014947), gap-junction abnormalities (MESH:C562538), mitochondrial dysfunction (MESH:D028361), atrio-ventricular block (MESH:C535326), ECG (MESH:C566733), sleep disorders (MESH:D012893), atrial and (MESH:D064752), QT prolongation (MESH:D008133), NSVT (MESH:D017180), Sleep Apnea (MESH:D012891), Ventricular alterations (MESH:D014693), cardiac abnormality (MESH:D018376), LAE (MESH:D059446), HFrEF (MESH:D054143), HF (MESH:D006333), atrial conduction abnormalities (MESH:C563984), torsades de pointes (MESH:D016171), OSA (MESH:D020181), cardiac disease (MESH:D006331), interatrial block (MESH:D000074021), QT dispersion (MESH:C563184), vagal (MESH:C536827), cardiac remodeling (MESH:D020257), LV hypertrophy (MESH:D006984), Atrial Fibrillation (MESH:D001281), ectopy (MESH:D050030), cardiovascular disease (MESH:D002318), AV block (MESH:D054537), Atrial abnormalities (MESH:D000014), thrombotic (MESH:D013927), eye movement (MESH:D015835), collapse (MESH:D001261), apnea (MESH:D001049), CSA (MESH:D020182), sinus pauses (MESH:D054138)
- **Chemicals:** aldosterone (MESH:D000450), PR (MESH:D011221), O2 (MESH:D010100), calcium (MESH:D002118), Bilevel (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** S in I

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12942396/full.md

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Source: https://tomesphere.com/paper/PMC12942396