# Spontaneous coronary artery dissection and fibromuscular dysplasia: insights into recent developments

**Authors:** Ayah Eltabbakh, Ahmed Khudair, Aiman Khudair, Salim Fredericks

PMC · DOI: 10.3389/fcvm.2024.1409278 · Frontiers in Cardiovascular Medicine · 2024-05-31

## TL;DR

This paper reviews recent findings on the link between two rare heart conditions, SCAD and FMD, focusing on their connection, diagnosis, and treatment challenges.

## Contribution

The paper highlights recent genetic and clinical insights into the association between SCAD and FMD, emphasizing the need for better screening and management strategies.

## Key findings

- FMD prevalence in SCAD patients ranges widely due to varying screening methods.
- A genetic link between SCAD and FMD has been recently identified.
- Physical exercise may be beneficial but remains understudied in managing SCAD and FMD.

## Abstract

Spontaneous coronary artery dissection (SCAD), an uncommon cause of acute coronary syndrome, continues to be a poorly understood disease predominantly affecting females. It is characterized by an abrupt separation in the coronary arterial wall due to intramural bleeding. Fibromuscular dysplasia (FMD) is a non-atherosclerotic arteriopathy manifesting in medium and small-sized arteries. It is a concomitant disease found among SCAD patients. In some studies, FMD prevalence in SCAD patients ranges between 25%–86%, which can be explained through varying screening techniques or modalities. The potential association has been elucidated in some studies; notably, not only has a genetic link been recently delineated between SCAD and FMD, but there is data to suggest that FMD not only can predispose to SCAD but can also be a potential predictor of its recurrence. However, a clear-cut correlation between the two has still not been established due to conflicting reports in the literature. To further dive into its pathology, it is crucial to highlight the importance of systematic screening in SCAD in order to identify associated risk factors and to be used as a method of FMD detection in such patients. Together, the two pathologies pose unique challenges in understanding its pathophysiology, diagnosis and management, as there is no clear evidence of a definitive treatment plan for patients with SCAD and FMD. A potentially beneficial modality of management is physical exercise, which is currently understudied in the long-term approach to treatment for patients with concomitant SCAD and FMD. Limited research in this field brings disadvantages to the understanding of the association between these two diseases, in order to give rise to better management recommendations. This mini-review aims to highlight the recent developments in the association between SCAD and FMD, its potential genetic association and some insights in screening, diagnosis, and management.

## Linked entities

- **Diseases:** Fibromuscular dysplasia (MONDO:0006761), acute coronary syndrome (MONDO:0005542)

## Full-text entities

- **Diseases:** bleeding (MESH:D006470), FMD (MESH:D005352), SCAD (MESH:C565153), acute coronary syndrome (MESH:D054058), atherosclerotic arteriopathy (MESH:D050197)
- **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/PMC11176522/full.md

## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC11176522/full.md

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Source: https://tomesphere.com/paper/PMC11176522