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Coronary artery disease in adults with anomalous aortic origin of a coronary artery

OBJECTIVES: This study sought to characterize coronary artery disease (CAD) among adults diagnosed with an anomalous aortic origin of a coronary artery (AAOCA). We hypothesized that coronaries with anomalous origins have more severe CAD stenosis than coronaries with normal origins. METHODS: This sin...

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Autores principales: Jiang, Michael X., Brinza, Ellen K., Ghobrial, Joanna, Tucker, Dominique L., Gupta, Sohini, Rajeswaran, Jeevanantham, Karamlou, Tara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390708/
https://www.ncbi.nlm.nih.gov/pubmed/36004264
http://dx.doi.org/10.1016/j.xjon.2022.04.022
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author Jiang, Michael X.
Brinza, Ellen K.
Ghobrial, Joanna
Tucker, Dominique L.
Gupta, Sohini
Rajeswaran, Jeevanantham
Karamlou, Tara
author_facet Jiang, Michael X.
Brinza, Ellen K.
Ghobrial, Joanna
Tucker, Dominique L.
Gupta, Sohini
Rajeswaran, Jeevanantham
Karamlou, Tara
author_sort Jiang, Michael X.
collection PubMed
description OBJECTIVES: This study sought to characterize coronary artery disease (CAD) among adults diagnosed with an anomalous aortic origin of a coronary artery (AAOCA). We hypothesized that coronaries with anomalous origins have more severe CAD stenosis than coronaries with normal origins. METHODS: This single-center study of 763 adults with AAOCA consisted of 620 patients from our cardiac catheterization database (1958-2009) and 273 patients from electronic medical records query (2010-2021). Within left main, anterior descending, circumflex, and right coronary arteries, the CAD stenosis severity, assessed by invasive or computer tomography angiography, was modeled with coronary-level variables (presence of an anomalous origin) and patient-level variables (age, sex, comorbidities, and which of the four coronaries was anomalous). RESULTS: Of the 763 patients, 472 (60%) had obstructive CAD, of whom, 142/472 (30%) had obstructive CAD only in the anomalous coronary. Multivariable modeling showed similar CAD stenosis severity between coronaries with anomalous versus normal origins (P = .8). Compared with AAOCA of other coronaries, the anomalous circumflex was diagnosed at older ages (59.7 ± 11.1 vs 54.3 ± 15.8 years, P < .0001) and was associated with increased stenosis in all coronaries (odds ratio, 2.7; 95% confidence interval, 2.2-3.4, P < .0001). CONCLUSIONS: Among adults diagnosed with AAOCA, the anomalous origin did not appear to increase the severity of CAD within the anomalous coronary. In contrast to the circumflex, AAOCA of the other vessels may contribute a greater ischemic burden when they present symptomatically at younger ages with less CAD. Future research should investigate the interaction between AAOCA, CAD, and ischemic risk to guide interventions.
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spelling pubmed-93907082022-08-23 Coronary artery disease in adults with anomalous aortic origin of a coronary artery Jiang, Michael X. Brinza, Ellen K. Ghobrial, Joanna Tucker, Dominique L. Gupta, Sohini Rajeswaran, Jeevanantham Karamlou, Tara JTCVS Open Adult: Coronary OBJECTIVES: This study sought to characterize coronary artery disease (CAD) among adults diagnosed with an anomalous aortic origin of a coronary artery (AAOCA). We hypothesized that coronaries with anomalous origins have more severe CAD stenosis than coronaries with normal origins. METHODS: This single-center study of 763 adults with AAOCA consisted of 620 patients from our cardiac catheterization database (1958-2009) and 273 patients from electronic medical records query (2010-2021). Within left main, anterior descending, circumflex, and right coronary arteries, the CAD stenosis severity, assessed by invasive or computer tomography angiography, was modeled with coronary-level variables (presence of an anomalous origin) and patient-level variables (age, sex, comorbidities, and which of the four coronaries was anomalous). RESULTS: Of the 763 patients, 472 (60%) had obstructive CAD, of whom, 142/472 (30%) had obstructive CAD only in the anomalous coronary. Multivariable modeling showed similar CAD stenosis severity between coronaries with anomalous versus normal origins (P = .8). Compared with AAOCA of other coronaries, the anomalous circumflex was diagnosed at older ages (59.7 ± 11.1 vs 54.3 ± 15.8 years, P < .0001) and was associated with increased stenosis in all coronaries (odds ratio, 2.7; 95% confidence interval, 2.2-3.4, P < .0001). CONCLUSIONS: Among adults diagnosed with AAOCA, the anomalous origin did not appear to increase the severity of CAD within the anomalous coronary. In contrast to the circumflex, AAOCA of the other vessels may contribute a greater ischemic burden when they present symptomatically at younger ages with less CAD. Future research should investigate the interaction between AAOCA, CAD, and ischemic risk to guide interventions. Elsevier 2022-04-20 /pmc/articles/PMC9390708/ /pubmed/36004264 http://dx.doi.org/10.1016/j.xjon.2022.04.022 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Adult: Coronary
Jiang, Michael X.
Brinza, Ellen K.
Ghobrial, Joanna
Tucker, Dominique L.
Gupta, Sohini
Rajeswaran, Jeevanantham
Karamlou, Tara
Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title_full Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title_fullStr Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title_full_unstemmed Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title_short Coronary artery disease in adults with anomalous aortic origin of a coronary artery
title_sort coronary artery disease in adults with anomalous aortic origin of a coronary artery
topic Adult: Coronary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9390708/
https://www.ncbi.nlm.nih.gov/pubmed/36004264
http://dx.doi.org/10.1016/j.xjon.2022.04.022
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