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Clinical significance of subclinical atherosclerosis in retinal vein occlusion
Retinal vein occlusion (RVO) is associated with atherosclerotic cardiovascular risk factors; however, its association with the specific markers of subclinical atherosclerosis has not yet been established. To investigate this association, we compared 70 patients with RVO to 70 age- and sex-matched pa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184809/ https://www.ncbi.nlm.nih.gov/pubmed/34099806 http://dx.doi.org/10.1038/s41598-021-91401-1 |
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author | Lyu, Minhyung Lee, Yonggu Kim, Byung Sik Kim, Hyun-Jin Hong, Rimkyung Shin, Yong Un Cho, Heeyoon Shin, Jeong-Hun |
author_facet | Lyu, Minhyung Lee, Yonggu Kim, Byung Sik Kim, Hyun-Jin Hong, Rimkyung Shin, Yong Un Cho, Heeyoon Shin, Jeong-Hun |
author_sort | Lyu, Minhyung |
collection | PubMed |
description | Retinal vein occlusion (RVO) is associated with atherosclerotic cardiovascular risk factors; however, its association with the specific markers of subclinical atherosclerosis has not yet been established. To investigate this association, we compared 70 patients with RVO to 70 age- and sex-matched patients without RVO. Low-density lipoprotein cholesterol (LDL-C) levels and brachial-ankle pulse wave velocity (baPWV) were significantly higher in the RVO group than in the control group. Carotid plaques (54.3% vs. 28.6%, p = 0.004) were more frequent in the RVO group. Multivariate logistic regression analysis showed that the presence of carotid plaques (odds ratio [OR]: 3.15, 95% confidence interval [CI] 1.38–7.16, p = 0.006), as well as smoking, LDL-C level, and baPWV were associated with RVO. Additionally, a multinomial logistic regression model showed that the presence of carotid plaques (OR: 3.94, 95% CI 1.65–9.41, p = 0.002) and LDL-C level were associated with branch RVO, whereas smoking and baPWV were associated with central RVO. In conclusion, RVO was associated with subclinical atherosclerosis markers, including carotid plaques and baPWV. These results support the hypothesis that atherosclerosis contributes to the etiology of RVO and suggest the evaluation of subclinical atherosclerosis in patients with RVO. |
format | Online Article Text |
id | pubmed-8184809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81848092021-06-08 Clinical significance of subclinical atherosclerosis in retinal vein occlusion Lyu, Minhyung Lee, Yonggu Kim, Byung Sik Kim, Hyun-Jin Hong, Rimkyung Shin, Yong Un Cho, Heeyoon Shin, Jeong-Hun Sci Rep Article Retinal vein occlusion (RVO) is associated with atherosclerotic cardiovascular risk factors; however, its association with the specific markers of subclinical atherosclerosis has not yet been established. To investigate this association, we compared 70 patients with RVO to 70 age- and sex-matched patients without RVO. Low-density lipoprotein cholesterol (LDL-C) levels and brachial-ankle pulse wave velocity (baPWV) were significantly higher in the RVO group than in the control group. Carotid plaques (54.3% vs. 28.6%, p = 0.004) were more frequent in the RVO group. Multivariate logistic regression analysis showed that the presence of carotid plaques (odds ratio [OR]: 3.15, 95% confidence interval [CI] 1.38–7.16, p = 0.006), as well as smoking, LDL-C level, and baPWV were associated with RVO. Additionally, a multinomial logistic regression model showed that the presence of carotid plaques (OR: 3.94, 95% CI 1.65–9.41, p = 0.002) and LDL-C level were associated with branch RVO, whereas smoking and baPWV were associated with central RVO. In conclusion, RVO was associated with subclinical atherosclerosis markers, including carotid plaques and baPWV. These results support the hypothesis that atherosclerosis contributes to the etiology of RVO and suggest the evaluation of subclinical atherosclerosis in patients with RVO. Nature Publishing Group UK 2021-06-07 /pmc/articles/PMC8184809/ /pubmed/34099806 http://dx.doi.org/10.1038/s41598-021-91401-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lyu, Minhyung Lee, Yonggu Kim, Byung Sik Kim, Hyun-Jin Hong, Rimkyung Shin, Yong Un Cho, Heeyoon Shin, Jeong-Hun Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title | Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title_full | Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title_fullStr | Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title_full_unstemmed | Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title_short | Clinical significance of subclinical atherosclerosis in retinal vein occlusion |
title_sort | clinical significance of subclinical atherosclerosis in retinal vein occlusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184809/ https://www.ncbi.nlm.nih.gov/pubmed/34099806 http://dx.doi.org/10.1038/s41598-021-91401-1 |
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