# Cardiovascular Involvement in Systemic Lupus Erythematosus: Focus on Arrhythmias

**Authors:** Monica Claudia Dobos, Veronica Ungurean, Diana Elena Costan, Mara Russu, Anca Ouatu, Paula Cristina Morariu, Alexandru Florinel Oancea, Maria Mihaela Godun, Diana-Elena Floria, Dragos Traian Marcu, Genoveva Livia Baroi, Silviu Marcel Stanciu, Anton Knieling, Daniela Maria Tanase, Codrina Ancuta, Mariana Floria

PMC · DOI: 10.3390/diagnostics16030372 · Diagnostics · 2026-01-23

## TL;DR

This review highlights how heart rhythm problems are a significant but often overlooked issue in patients with systemic lupus erythematosus.

## Contribution

The paper emphasizes the underrecognized role of arrhythmias in SLE and advocates for a multidisciplinary approach to improve detection and treatment.

## Key findings

- Cardiac arrhythmias in SLE are linked to structural heart damage, inflammation, and treatment side effects.
- Current data on how medications affect arrhythmias in SLE are limited and inconsistent.
- Early detection and coordinated care are crucial to reducing cardiovascular complications in SLE patients.

## Abstract

Background: Cardiovascular implications in systemic lupus erythematosus (SLE) are common and varied, including impacts on the pericardium, myocardium, valves, coronary arteries, and conduction system; all of these could be potential substrates or triggers of cardiac arrhythmias by interfering with disease severity and specific medication. Therefore, this narrative review aimed to assess the cardiac involvement in SLE underlying, mainly, cardiac arrhythmias. Methods: We analyzed studies, published between 2015 and 2025 on PubMed, which explore cardiovascular involvement with a focus on arrhythmias in SLE from the perspectives of epidemiology, underlying mechanisms, diagnostic techniques, and the impact of standard and biologic therapies. Results: The cardiac manifestation of LES (lupus pericarditis, lupus myocarditis, Libman–Sacks endocarditis, coronary artery disease, coronary vasculitis or myocardial fibrosis) represents a substrate for arrhythmia risk. These substrates, in association with other arrhythmias mechanisms considered as triggers or conduction abnormalities, determined arrhythmogenic conditions in these patients. In addition to structural heart disease, arrhythmias in SLE are caused by ongoing inflammation, immune system irregularities, microvascular problems, autonomic imbalance, oxidative stress, and side effects from treatments. Despite this complex background, arrhythmias are often overlooked and not routinely investigated in SLE care. Data that show how disease-modifying drugs may affect arrhythmias are limited and inconsistent, highlighting significant gaps in knowledge. Cardiac arrhythmias are a significant but, as yet, insufficiently underrecognized aspect of SLE, with serious implications for prognosis. Conclusions: Systemic lupus erythematosus causes cardiovascular involvement that is associated with arrhythmias through various and complexes mechanisms, mainly related to direct cardiovascular structural damage, systemic inflammation or specific therapies. Data on arrhythmias secondary to cardiovascular damage in patients with SLE in the literature are limited. Therefore, early detection of electrical issues, regular cardiovascular evaluation in high-risk patients, and careful management of treatment effects are vital. A coordinated, multidisciplinary cardio-rheumatology approach is essential to improving arrhythmia detection, tailoring treatments, and ultimately decreasing cardiovascular complications and deaths in SLE patients.

## Linked entities

- **Diseases:** systemic lupus erythematosus (MONDO:0007915), Libman–Sacks endocarditis (MONDO:0850223), coronary artery disease (MONDO:0005010)

## Full-text entities

- **Diseases:** systemic (MESH:D015619), lupus pericarditis (MESH:D010493), lupus myocarditis (MESH:D009205), Libman-Sacks endocarditis (MESH:D008180), myocardial fibrosis (MESH:D005355), conduction abnormalities (MESH:D054537), Cardiovascular Involvement (MESH:D002318), deaths (MESH:D003643), Arrhythmias (MESH:D001145), inflammation (MESH:D007249), coronary vasculitis (MESH:D014657), heart disease (MESH:D006331), coronary artery disease (MESH:D003324)
- **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/PMC12897435/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897435/full.md

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Source: https://tomesphere.com/paper/PMC12897435