Anomalous origin of the coronary artery: prevalence and coronary artery disease in adults undergoing coronary tomographic angiography

Background Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital coronary anomaly with the potential to cause adverse cardiac events. However, there is limited data on the association between AAOCA and coronary artery disease (CAD). Therefore, the aim of this study is to determin...

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Published inBMC cardiovascular disorders Vol. 24; no. 1; pp. 271 - 8
Main Authors Li, Kunyan, Hu, Ping, Luo, Xiaolin, Li, Furong, Chen, Ling, Zhao, Junyong, Wang, Zelan, Luo, Wenjian, Jin, Jun, Qin, Zhexue
Format Journal Article
LanguageEnglish
Published London BioMed Central 23.05.2024
BioMed Central Ltd
Springer Nature B.V
BMC
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ISSN1471-2261
1471-2261
DOI10.1186/s12872-024-03942-8

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Summary:Background Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital coronary anomaly with the potential to cause adverse cardiac events. However, there is limited data on the association between AAOCA and coronary artery disease (CAD). Therefore, the aim of this study is to determine the prevalence and symptoms of patients with AAOCA, as well as investigate the correlation between AAOCA and CAD in a population referred for coronary computed tomographic angiography (CTA). Methods and results All consecutive patients who underwent CTA from 2010 to 2021 were included. Characteristics, symptoms, coronary related adverse events and CTA information were reviewed by medical records. Separate multivariable cumulative logistic regressions were performed, using the stenosis severity in each of the four coronaries as individual responses and as a combined patient clustered response. Finally, we identified 207 adult patients with AAOCA, the prevalence of AAOCA is 0.23% (207/90,501). Moreover, this study found no significant association between AAOCA and CAD. AAOCA did not contribute to higher rates of hospitalization or adverse cardiac events, including calcification. Conclusion AAOCA is a rare congenital disease that is not associated with increased presence of obstructive CAD in adults.
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ISSN:1471-2261
1471-2261
DOI:10.1186/s12872-024-03942-8