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The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease
OBJECTIVE: The purpose of this study was to evaluate the effect of choroidal thickness and tear vascular endothelial growth factor A (VEGFA) as biomarkers of coronary artery disease (CAD). METHODS: This study was a retrospective observational case–control trial. A total of 637 patients who underwent...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538601/ https://www.ncbi.nlm.nih.gov/pubmed/37756415 http://dx.doi.org/10.1097/MCA.0000000000001279 |
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author | Zhou, Tingquan Wan, Ting Jin, Xian Chen, Yu Shen, Chengxing |
author_facet | Zhou, Tingquan Wan, Ting Jin, Xian Chen, Yu Shen, Chengxing |
author_sort | Zhou, Tingquan |
collection | PubMed |
description | OBJECTIVE: The purpose of this study was to evaluate the effect of choroidal thickness and tear vascular endothelial growth factor A (VEGFA) as biomarkers of coronary artery disease (CAD). METHODS: This study was a retrospective observational case–control trial. A total of 637 patients who underwent coronary angiography to assess their coronary artery status were included. The patients were divided into two groups: 200 people in the No CAD group and 437 people in the CAD group. We evaluated the choroidal thickness of the right foveal membrane in all patients through optical coherence tomography angiography examination. We also collected tear samples from patients to measure VEGFA. The ROC curve and its area under the curve (AUC) were used for analysis. RESULTS: The central foveal choroid in the No CAD group was significantly thicker than that in the CAD group (289.09 μm ± 38.41; 229.03 μm ± 33.44, P < 0.01). The tear VEGFA in the CAD group was higher than that in the No CAD group (706.15 ng/mL ± 147.42; 419.66 ng/mL ± 105.85, P < 0.01). Spearman analysis showed that the correlation between choroidal thickness and Gensini score was –0.7387 (P < 0.01). The correlation between tear VEGFA level and Gensini score was 0.8636 (P < 0.01). Taking choroidal thickness and tear VEGFA as independent variables, we obtained AUC = 0.9647 (95% CI 0.9506–0.9789, P < 0.01) through binary logic regression and ROC curve analysis. CONCLUSION: The combination of choroidal thickness and tear VEGFA in patients can serve as a clinical marker of CAD and its severity. |
format | Online Article Text |
id | pubmed-10538601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-105386012023-09-29 The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease Zhou, Tingquan Wan, Ting Jin, Xian Chen, Yu Shen, Chengxing Coron Artery Dis Original Research OBJECTIVE: The purpose of this study was to evaluate the effect of choroidal thickness and tear vascular endothelial growth factor A (VEGFA) as biomarkers of coronary artery disease (CAD). METHODS: This study was a retrospective observational case–control trial. A total of 637 patients who underwent coronary angiography to assess their coronary artery status were included. The patients were divided into two groups: 200 people in the No CAD group and 437 people in the CAD group. We evaluated the choroidal thickness of the right foveal membrane in all patients through optical coherence tomography angiography examination. We also collected tear samples from patients to measure VEGFA. The ROC curve and its area under the curve (AUC) were used for analysis. RESULTS: The central foveal choroid in the No CAD group was significantly thicker than that in the CAD group (289.09 μm ± 38.41; 229.03 μm ± 33.44, P < 0.01). The tear VEGFA in the CAD group was higher than that in the No CAD group (706.15 ng/mL ± 147.42; 419.66 ng/mL ± 105.85, P < 0.01). Spearman analysis showed that the correlation between choroidal thickness and Gensini score was –0.7387 (P < 0.01). The correlation between tear VEGFA level and Gensini score was 0.8636 (P < 0.01). Taking choroidal thickness and tear VEGFA as independent variables, we obtained AUC = 0.9647 (95% CI 0.9506–0.9789, P < 0.01) through binary logic regression and ROC curve analysis. CONCLUSION: The combination of choroidal thickness and tear VEGFA in patients can serve as a clinical marker of CAD and its severity. Lippincott Williams & Wilkins 2023-11 2023-09-25 /pmc/articles/PMC10538601/ /pubmed/37756415 http://dx.doi.org/10.1097/MCA.0000000000001279 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Research Zhou, Tingquan Wan, Ting Jin, Xian Chen, Yu Shen, Chengxing The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title | The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title_full | The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title_fullStr | The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title_full_unstemmed | The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title_short | The clinical implications of choroidal thickness combined with tear VEGFA in coronary artery disease |
title_sort | clinical implications of choroidal thickness combined with tear vegfa in coronary artery disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538601/ https://www.ncbi.nlm.nih.gov/pubmed/37756415 http://dx.doi.org/10.1097/MCA.0000000000001279 |
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