# Anatomical Variants of the Origin of the Coronary Arteries: A Systematic Review and Meta-Analysis of Prevalence

**Authors:** Juan José Valenzuela Fuenzalida, Emelyn Sofia Becerra-Rodriguez, Alonso Sebastián Quivira Muñoz, Belén Baez Flores, Catalina Escalona Manzo, Mathias Orellana-Donoso, Pablo Nova-Baeza, Alejandra Suazo-Santibañez, Alejandro Bruna-Mejias, Juan Sanchis-Gimeno, Héctor Gutiérrez-Espinoza, Guinevere Granite

PMC · DOI: 10.3390/diagnostics14131458 · Diagnostics · 2024-07-08

## TL;DR

This study reviews and analyzes the prevalence of anatomical variants in coronary artery origins and their clinical implications.

## Contribution

The study provides a systematic review and meta-analysis of coronary artery origin variants and their prevalence.

## Key findings

- The pooled prevalence of coronary artery origin variants was found to be 1%.
- The funnel plot showed significant asymmetry, indicating potential bias or heterogeneity in the data.

## Abstract

Purpose: The most common anomaly is an anomalous left coronary artery originating from the pulmonary artery. These variants can be different and depend on the location as well as how they present themselves in their anatomical distribution and their symptomatological relationship. For these reasons, this review aims to identify the variants of the coronary artery and how they are associated with different clinical conditions. Methods: The databases Medline, Scopus, Web of Science, Google Scholar, CINAHL, and LILACS were researched until January 2024. Two authors independently performed the search, study selection, and data extraction. Methodological quality was evaluated using an assurance tool for anatomical studies (AQUA). Pooled prevalence was estimated using a random effects model. Results: A total of 39 studies met the established selection criteria. In this study, 21 articles with a total of 578,868 subjects were included in the meta-analysis. The coronary artery origin variant was 1% (CI = 0.8–1.2%). For this third sample, the funnel plot graph showed an important asymmetry, with a p-value of 0.162, which is directly associated with this asymmetry. Conclusions: It is recommended that patients whose diagnosis was made incidentally and in the absence of symptoms undergo periodic controls to prevent future complications, including death. Finally, we believe that further studies could improve the anatomical, embryological, and physiological understanding of this variant in the heart.

## Full-text entities

- **Diseases:** death (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11241028/full.md

## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC11241028/full.md

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Source: https://tomesphere.com/paper/PMC11241028