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Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups

BACKGROUND: Coronary artery ectasia (CAE) is an angiographic finding of abnormal coronary dilatation. Inflammation plays a major role in all phases of atherosclerosis. We investigated the relationship between CAE and serum high-sensitivity C-reactive protein (hs-CRP) and interleukin-6 (IL-6) levels...

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Autores principales: Fan, Cheng-Hui, Hao, Ying, Liu, Yong-Hua, Li, Xiao-Lin, Huang, Zhen-Hao, Luo, Yu, Li, Rui-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353781/
https://www.ncbi.nlm.nih.gov/pubmed/32652935
http://dx.doi.org/10.1186/s12872-020-01604-z
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author Fan, Cheng-Hui
Hao, Ying
Liu, Yong-Hua
Li, Xiao-Lin
Huang, Zhen-Hao
Luo, Yu
Li, Rui-Lin
author_facet Fan, Cheng-Hui
Hao, Ying
Liu, Yong-Hua
Li, Xiao-Lin
Huang, Zhen-Hao
Luo, Yu
Li, Rui-Lin
author_sort Fan, Cheng-Hui
collection PubMed
description BACKGROUND: Coronary artery ectasia (CAE) is an angiographic finding of abnormal coronary dilatation. Inflammation plays a major role in all phases of atherosclerosis. We investigated the relationship between CAE and serum high-sensitivity C-reactive protein (hs-CRP) and interleukin-6 (IL-6) levels to test our hypothesis that patient age is associated with the efficacy of anti-inflammatory therapy for CAE. METHODS: We conducted a prospective analysis of 217 patients with CAE treated at the Department of Cardiology, Shanghai East Hospital, Ji’an Campus and the Baoshan People’s Hospital, from January 1, 2015 to July 30, 2019. Baseline data of patients, including sex; age; and history of hypertension, hyperlipidemia, and diabetes, were collected from patient medical records. Study participants were grouped by age as follows: CAE-A (n = 60, age ≤ 50 years), CAE-B (n = 83, 50 years <age ≤ 70 years), and CAE-C (n = 74, age > 70). Additionally, there was a control (NC) group (n = 73) with normal coronary arteries. RESULTS: All patients received oral rosuvastatin therapy (10 mg, QN quaque nocte) when they were diagnosed with CAE and maintained good follow-up, with a loss rate of 0.0% at the end of the 6-month follow-up. The NC group received regular symptom-relieving treatments and rosuvastatin therapy. Of these four groups, the inflammatory markers, hs-CRP and IL-6, were significantly higher in patients with CAE than in the NCs (p < 0.05). Post-hoc tests showed that hs-CRP and Il-6 levels had significant differences between the CAE-A and CAE-C groups (P = 0.048, P = 0.025). Logistic regression analysis showed that hs-CRP (OR = 1.782, 95% CI: 1.124–2.014, P = 0.021) and IL-6 (OR = 1.584, 95% CI: 1.112–1.986, P = 0.030) were independent predictors of CAE. The inflammatory markers were higher in the CAE-A group than in the CAE-B group and higher in the CAE-B group than in the CAE-C group. Follow-up after 6 months of rosuvastatin therapy showed a significantly greater reduction in hs-CRP and IL-6 levels in the CAE-A group than in the CAE-B group, which again were greater in the CAE-B group than in the CAE-C group. CONCLUSIONS: Anti-inflammatory therapy using rosuvastatin was more effective in younger CAE patients, indicating the need for early statin therapy in CAE.
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spelling pubmed-73537812020-07-15 Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups Fan, Cheng-Hui Hao, Ying Liu, Yong-Hua Li, Xiao-Lin Huang, Zhen-Hao Luo, Yu Li, Rui-Lin BMC Cardiovasc Disord Research Article BACKGROUND: Coronary artery ectasia (CAE) is an angiographic finding of abnormal coronary dilatation. Inflammation plays a major role in all phases of atherosclerosis. We investigated the relationship between CAE and serum high-sensitivity C-reactive protein (hs-CRP) and interleukin-6 (IL-6) levels to test our hypothesis that patient age is associated with the efficacy of anti-inflammatory therapy for CAE. METHODS: We conducted a prospective analysis of 217 patients with CAE treated at the Department of Cardiology, Shanghai East Hospital, Ji’an Campus and the Baoshan People’s Hospital, from January 1, 2015 to July 30, 2019. Baseline data of patients, including sex; age; and history of hypertension, hyperlipidemia, and diabetes, were collected from patient medical records. Study participants were grouped by age as follows: CAE-A (n = 60, age ≤ 50 years), CAE-B (n = 83, 50 years <age ≤ 70 years), and CAE-C (n = 74, age > 70). Additionally, there was a control (NC) group (n = 73) with normal coronary arteries. RESULTS: All patients received oral rosuvastatin therapy (10 mg, QN quaque nocte) when they were diagnosed with CAE and maintained good follow-up, with a loss rate of 0.0% at the end of the 6-month follow-up. The NC group received regular symptom-relieving treatments and rosuvastatin therapy. Of these four groups, the inflammatory markers, hs-CRP and IL-6, were significantly higher in patients with CAE than in the NCs (p < 0.05). Post-hoc tests showed that hs-CRP and Il-6 levels had significant differences between the CAE-A and CAE-C groups (P = 0.048, P = 0.025). Logistic regression analysis showed that hs-CRP (OR = 1.782, 95% CI: 1.124–2.014, P = 0.021) and IL-6 (OR = 1.584, 95% CI: 1.112–1.986, P = 0.030) were independent predictors of CAE. The inflammatory markers were higher in the CAE-A group than in the CAE-B group and higher in the CAE-B group than in the CAE-C group. Follow-up after 6 months of rosuvastatin therapy showed a significantly greater reduction in hs-CRP and IL-6 levels in the CAE-A group than in the CAE-B group, which again were greater in the CAE-B group than in the CAE-C group. CONCLUSIONS: Anti-inflammatory therapy using rosuvastatin was more effective in younger CAE patients, indicating the need for early statin therapy in CAE. BioMed Central 2020-07-11 /pmc/articles/PMC7353781/ /pubmed/32652935 http://dx.doi.org/10.1186/s12872-020-01604-z Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Fan, Cheng-Hui
Hao, Ying
Liu, Yong-Hua
Li, Xiao-Lin
Huang, Zhen-Hao
Luo, Yu
Li, Rui-Lin
Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title_full Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title_fullStr Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title_full_unstemmed Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title_short Anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
title_sort anti-inflammatory effects of rosuvastatin treatment on coronary artery ectasia patients of different age groups
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353781/
https://www.ncbi.nlm.nih.gov/pubmed/32652935
http://dx.doi.org/10.1186/s12872-020-01604-z
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