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Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis

BACKGROUND: Liraglutide is a novel, long-acting glucagon-like peptide-1 (GLP-1) analogue used to treat type 2 diabetes mellitus. However, the cardiovascular safety and benefits of liraglutide treatment on type 2 diabetes patients remain in debate. In this study, we aimed to examine the overall cardi...

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Autores principales: Duan, Chun-Mei, Wan, Teng-Fei, Wang, Yue, Yang, Qing-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867782/
https://www.ncbi.nlm.nih.gov/pubmed/31725627
http://dx.doi.org/10.1097/MD.0000000000017860
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author Duan, Chun-Mei
Wan, Teng-Fei
Wang, Yue
Yang, Qing-Wu
author_facet Duan, Chun-Mei
Wan, Teng-Fei
Wang, Yue
Yang, Qing-Wu
author_sort Duan, Chun-Mei
collection PubMed
description BACKGROUND: Liraglutide is a novel, long-acting glucagon-like peptide-1 (GLP-1) analogue used to treat type 2 diabetes mellitus. However, the cardiovascular safety and benefits of liraglutide treatment on type 2 diabetes patients remain in debate. In this study, we aimed to examine the overall cardiovascular outcomes of liraglutide in patients with type 2 diabetes. METHODS: In this systematic review and meta-analysis, we searched the PubMed, Embase, and Web of Knowledge databases up to September 1st, 2017 for randomized trials in which type 2 diabetes patients were assigned to liraglutide and placebo or other comparators groups. RESULTS: Eight studies fulfilled the eligibility criteria for inclusion and 14,608 patients were analyzed in this systematic review and meta-analysis. We found patients in the liraglutide group had a lower risk of major cardiovascular events (MACE) (RR = 0.89, 95% CI: 0.82–0.96, P = .002), acute myocardial infarction (AMI) (RR = 0.85, 95% CI: 0.74–0.99, P = .036), all-cause death (RR = 0.84, 95% CI: 0.74–0.96, P = .009), and cardiovascular death (RR = 0.77, 95% CI: 0.65–0.91, P = .002) than all comparator groups. However, liraglutide treatment did not decrease incidence of stroke (RR = 0.86, 95% CI: 0.70–1.04, P = .124). But among the MACE subgroups analysis, a significant reduction of MACE with liraglutide was only observed in placebo-controlled trials (RR = 0.89, 95% CI: 0.83–0.96, P = .004) but not in studies concerning other comparators (RR = 0.58, 95% CI: 0.29–1.16, P = .122). CONCLUSIONS: In conclusion, our results suggest that liraglutide treatment decreases the risk of MACE, AMI, all-cause death and cardiovascular death among patients with type 2 diabetes.
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spelling pubmed-68677822020-01-14 Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis Duan, Chun-Mei Wan, Teng-Fei Wang, Yue Yang, Qing-Wu Medicine (Baltimore) 3400 BACKGROUND: Liraglutide is a novel, long-acting glucagon-like peptide-1 (GLP-1) analogue used to treat type 2 diabetes mellitus. However, the cardiovascular safety and benefits of liraglutide treatment on type 2 diabetes patients remain in debate. In this study, we aimed to examine the overall cardiovascular outcomes of liraglutide in patients with type 2 diabetes. METHODS: In this systematic review and meta-analysis, we searched the PubMed, Embase, and Web of Knowledge databases up to September 1st, 2017 for randomized trials in which type 2 diabetes patients were assigned to liraglutide and placebo or other comparators groups. RESULTS: Eight studies fulfilled the eligibility criteria for inclusion and 14,608 patients were analyzed in this systematic review and meta-analysis. We found patients in the liraglutide group had a lower risk of major cardiovascular events (MACE) (RR = 0.89, 95% CI: 0.82–0.96, P = .002), acute myocardial infarction (AMI) (RR = 0.85, 95% CI: 0.74–0.99, P = .036), all-cause death (RR = 0.84, 95% CI: 0.74–0.96, P = .009), and cardiovascular death (RR = 0.77, 95% CI: 0.65–0.91, P = .002) than all comparator groups. However, liraglutide treatment did not decrease incidence of stroke (RR = 0.86, 95% CI: 0.70–1.04, P = .124). But among the MACE subgroups analysis, a significant reduction of MACE with liraglutide was only observed in placebo-controlled trials (RR = 0.89, 95% CI: 0.83–0.96, P = .004) but not in studies concerning other comparators (RR = 0.58, 95% CI: 0.29–1.16, P = .122). CONCLUSIONS: In conclusion, our results suggest that liraglutide treatment decreases the risk of MACE, AMI, all-cause death and cardiovascular death among patients with type 2 diabetes. Wolters Kluwer Health 2019-11-15 /pmc/articles/PMC6867782/ /pubmed/31725627 http://dx.doi.org/10.1097/MD.0000000000017860 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 3400
Duan, Chun-Mei
Wan, Teng-Fei
Wang, Yue
Yang, Qing-Wu
Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title_full Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title_fullStr Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title_full_unstemmed Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title_short Cardiovascular outcomes of liraglutide in patients with type 2 diabetes: A systematic review and meta-analysis
title_sort cardiovascular outcomes of liraglutide in patients with type 2 diabetes: a systematic review and meta-analysis
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867782/
https://www.ncbi.nlm.nih.gov/pubmed/31725627
http://dx.doi.org/10.1097/MD.0000000000017860
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