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Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease

BACKGROUND: Proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors have been documented with significantly reduction in LDL cholesterol levels and cardiovascular events. However, evidence regarding the impact of PCSK9 inhibitors on coronary calcification is limited. METHODS: Eligible patie...

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Autores principales: Gao, Fei, Li, Yue Ping, Ma, Xiao Teng, Wang, Zhi Jian, Shi, Dong Mei, Zhou, Yu Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120536/
https://www.ncbi.nlm.nih.gov/pubmed/35600486
http://dx.doi.org/10.3389/fcvm.2022.907662
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author Gao, Fei
Li, Yue Ping
Ma, Xiao Teng
Wang, Zhi Jian
Shi, Dong Mei
Zhou, Yu Jie
author_facet Gao, Fei
Li, Yue Ping
Ma, Xiao Teng
Wang, Zhi Jian
Shi, Dong Mei
Zhou, Yu Jie
author_sort Gao, Fei
collection PubMed
description BACKGROUND: Proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors have been documented with significantly reduction in LDL cholesterol levels and cardiovascular events. However, evidence regarding the impact of PCSK9 inhibitors on coronary calcification is limited. METHODS: Eligible patients with intermediate coronary lesions and elevated LDL cholesterol values were randomized to either alirocumab 75 mg Q2W plus statin (atorvastatin 20 mg/day or rosuvastatin 10 mg/day) therapy or standard statin therapy. Calcium score based on coronary computed tomographic angiography at baseline and follow up were compared. RESULTS: Compared with baseline levels, LDL cholesterol were significantly decreased in both groups, while the absolute reduction of LDL cholesterol levels were higher in patients treated with alirocumab (1.69 ± 0.52 vs. 0.92 ± 0.60, P < 0.0001). Additionally, patients in alirocumab group demonstrated a significant reduction of Lp(a) levels, whereas it was not observed in the standard statin group. Notably, greater increases in the percentage changes of CAC score (10.6% [6.3–23.3] vs. 2.9% [−6.7–8.3]; P < 0.0001) were observed in the statin group compared to the alirocumab group. Consistently, CAC progression was significantly lower in the alirocumab group than in the standard statin group (0.6 ± 2.2% vs. 2.7 ± 2.3%; P = 0.002). CONCLUSIONS: Study indicated that administration of the PCSK9 inhibitors to statins produced significantly lower rate of CAC progression in patients with coronary artery disease. Further studies with CAC progression and their clinical outcomes are needed. TRIAL REGISTRATION: ClinicalTrials.gov, Identifier: NCT04851769.
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spelling pubmed-91205362022-05-21 Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease Gao, Fei Li, Yue Ping Ma, Xiao Teng Wang, Zhi Jian Shi, Dong Mei Zhou, Yu Jie Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors have been documented with significantly reduction in LDL cholesterol levels and cardiovascular events. However, evidence regarding the impact of PCSK9 inhibitors on coronary calcification is limited. METHODS: Eligible patients with intermediate coronary lesions and elevated LDL cholesterol values were randomized to either alirocumab 75 mg Q2W plus statin (atorvastatin 20 mg/day or rosuvastatin 10 mg/day) therapy or standard statin therapy. Calcium score based on coronary computed tomographic angiography at baseline and follow up were compared. RESULTS: Compared with baseline levels, LDL cholesterol were significantly decreased in both groups, while the absolute reduction of LDL cholesterol levels were higher in patients treated with alirocumab (1.69 ± 0.52 vs. 0.92 ± 0.60, P < 0.0001). Additionally, patients in alirocumab group demonstrated a significant reduction of Lp(a) levels, whereas it was not observed in the standard statin group. Notably, greater increases in the percentage changes of CAC score (10.6% [6.3–23.3] vs. 2.9% [−6.7–8.3]; P < 0.0001) were observed in the statin group compared to the alirocumab group. Consistently, CAC progression was significantly lower in the alirocumab group than in the standard statin group (0.6 ± 2.2% vs. 2.7 ± 2.3%; P = 0.002). CONCLUSIONS: Study indicated that administration of the PCSK9 inhibitors to statins produced significantly lower rate of CAC progression in patients with coronary artery disease. Further studies with CAC progression and their clinical outcomes are needed. TRIAL REGISTRATION: ClinicalTrials.gov, Identifier: NCT04851769. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9120536/ /pubmed/35600486 http://dx.doi.org/10.3389/fcvm.2022.907662 Text en Copyright © 2022 Gao, Li, Ma, Wang, Shi and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Gao, Fei
Li, Yue Ping
Ma, Xiao Teng
Wang, Zhi Jian
Shi, Dong Mei
Zhou, Yu Jie
Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title_full Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title_fullStr Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title_full_unstemmed Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title_short Effect of Alirocumab on Coronary Calcification in Patients With Coronary Artery Disease
title_sort effect of alirocumab on coronary calcification in patients with coronary artery disease
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120536/
https://www.ncbi.nlm.nih.gov/pubmed/35600486
http://dx.doi.org/10.3389/fcvm.2022.907662
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