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Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study

Retinal vascular occlusion (RVO), including retinal arterial occlusion and retinal vein occlusion, is a common retinal vascular disease that causes visual disturbance. The exact pathogenesis of RVO remains unclear. In all types of RVO patients, hyperlipidemia is more than twofold more common than in...

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Autores principales: Chien, Chien-Cheng, Chen, Po-Huang, Chung, Chi-Hsiang, Sun, Chien-An, Chien, Wu-Chien, Chien, Ke-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471930/
https://www.ncbi.nlm.nih.gov/pubmed/34574786
http://dx.doi.org/10.3390/ijerph18189864
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author Chien, Chien-Cheng
Chen, Po-Huang
Chung, Chi-Hsiang
Sun, Chien-An
Chien, Wu-Chien
Chien, Ke-Hung
author_facet Chien, Chien-Cheng
Chen, Po-Huang
Chung, Chi-Hsiang
Sun, Chien-An
Chien, Wu-Chien
Chien, Ke-Hung
author_sort Chien, Chien-Cheng
collection PubMed
description Retinal vascular occlusion (RVO), including retinal arterial occlusion and retinal vein occlusion, is a common retinal vascular disease that causes visual disturbance. The exact pathogenesis of RVO remains unclear. In all types of RVO patients, hyperlipidemia is more than twofold more common than in controls. Statins have been used to control blood cholesterol levels and have been found to reduce the risk of cardiovascular morbidity and mortality. Moreover, the immunomodulatory functions of statins may play a role in treating inflammatory diseases. This study aimed to evaluate whether patients taking statins have a lower risk of developing RVO compared to patients not taking statins. Adult patients with statins usage on the index date identified from the Taiwan National Health Insurance Research Database (NHIRD) between 2000 and 2013 were included. A threefold matched group was selected using age, sex, and year of index date for comparison. During the mean follow-up period of 12.87 ± 1.88 years, the cumulative incidence of RVO was significantly lower in the statin-user group (29.96 per 105 person-years [PYs]) than in the non-statin-user group (39.35 per 105 PYs). The results showed a lower cumulative incidence rate of RVO in patients prescribed statins than in those not prescribed statins (log-rank test, p = 0.020). The adjusting hazard ratio (HR) was significantly greater for RVO in the statin-user group (adjusted HR, 0.704; 95% CI, 0.591–0.873). Statin users had a decreased risk for all types of RVO development, including central retinal artery occlusion, arterial branch occlusion, central retinal vein occlusion, and branch retinal vein occlusion. In conclusion, patients undergoing statin treatment have a lower risk of developing RVO compared to patients not taking statins.
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spelling pubmed-84719302021-09-28 Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study Chien, Chien-Cheng Chen, Po-Huang Chung, Chi-Hsiang Sun, Chien-An Chien, Wu-Chien Chien, Ke-Hung Int J Environ Res Public Health Article Retinal vascular occlusion (RVO), including retinal arterial occlusion and retinal vein occlusion, is a common retinal vascular disease that causes visual disturbance. The exact pathogenesis of RVO remains unclear. In all types of RVO patients, hyperlipidemia is more than twofold more common than in controls. Statins have been used to control blood cholesterol levels and have been found to reduce the risk of cardiovascular morbidity and mortality. Moreover, the immunomodulatory functions of statins may play a role in treating inflammatory diseases. This study aimed to evaluate whether patients taking statins have a lower risk of developing RVO compared to patients not taking statins. Adult patients with statins usage on the index date identified from the Taiwan National Health Insurance Research Database (NHIRD) between 2000 and 2013 were included. A threefold matched group was selected using age, sex, and year of index date for comparison. During the mean follow-up period of 12.87 ± 1.88 years, the cumulative incidence of RVO was significantly lower in the statin-user group (29.96 per 105 person-years [PYs]) than in the non-statin-user group (39.35 per 105 PYs). The results showed a lower cumulative incidence rate of RVO in patients prescribed statins than in those not prescribed statins (log-rank test, p = 0.020). The adjusting hazard ratio (HR) was significantly greater for RVO in the statin-user group (adjusted HR, 0.704; 95% CI, 0.591–0.873). Statin users had a decreased risk for all types of RVO development, including central retinal artery occlusion, arterial branch occlusion, central retinal vein occlusion, and branch retinal vein occlusion. In conclusion, patients undergoing statin treatment have a lower risk of developing RVO compared to patients not taking statins. MDPI 2021-09-18 /pmc/articles/PMC8471930/ /pubmed/34574786 http://dx.doi.org/10.3390/ijerph18189864 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chien, Chien-Cheng
Chen, Po-Huang
Chung, Chi-Hsiang
Sun, Chien-An
Chien, Wu-Chien
Chien, Ke-Hung
Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title_full Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title_fullStr Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title_full_unstemmed Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title_short Association between Statins and Retinal Vascular Occlusion: A Population-Based Cohort Study
title_sort association between statins and retinal vascular occlusion: a population-based cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471930/
https://www.ncbi.nlm.nih.gov/pubmed/34574786
http://dx.doi.org/10.3390/ijerph18189864
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