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The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis

BACKGROUND: Atherosclerosis is a common inflammatory disease. Stem cell and endothelial progenitor cell treatments can improve cardiac function after myocardial infarction. Granulocyte colony-stimulating factor (G-CSF) is a mobilisation agent, mobilising stem cells from the bone marrow to circulatio...

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Autores principales: Liu, Manli, Liu, Kejian, Chen, Dongdong, Chen, Hongzhi, Sun, Kunming, Ju, Xinxin, Lan, Jiaojiao, Zhou, Yang, Wang, Weishan, Pang, Lijuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613364/
https://www.ncbi.nlm.nih.gov/pubmed/29138752
http://dx.doi.org/10.1155/2017/6705363
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author Liu, Manli
Liu, Kejian
Chen, Dongdong
Chen, Hongzhi
Sun, Kunming
Ju, Xinxin
Lan, Jiaojiao
Zhou, Yang
Wang, Weishan
Pang, Lijuan
author_facet Liu, Manli
Liu, Kejian
Chen, Dongdong
Chen, Hongzhi
Sun, Kunming
Ju, Xinxin
Lan, Jiaojiao
Zhou, Yang
Wang, Weishan
Pang, Lijuan
author_sort Liu, Manli
collection PubMed
description BACKGROUND: Atherosclerosis is a common inflammatory disease. Stem cell and endothelial progenitor cell treatments can improve cardiac function after myocardial infarction. Granulocyte colony-stimulating factor (G-CSF) is a mobilisation agent, mobilising stem cells from the bone marrow to circulation in the blood. G-CSF may constitute a treatment of atherosclerosis. We have conducted meta-analysis to evaluate the current evidence for the effect of G-CSF on the progression of atherosclerosis in animal models and to provide reference for preclinical experiments and future human clinical trials of atherosclerosis treatment. METHODS: We searched several databases and conducted a meta-analysis across seven articles using a random-effect model. All statistical analyses were performed using Review Manager Version 5.2 and Stata 12.0. RESULTS: We found that G-CSF therapy was associated with reduced atherosclerotic lesion area (weighted mean difference (WMD): 7.29%; 95% confidence interval (CI): 2.06–12.52%; P = 0.006). No significant differences in total serum cholesterol (P = 0.54) and triglyceride levels (P = 0.95) were noted in G-CSF treatment groups compared with controls. Multivariable metaregression analysis revealed that the animal type (rabbit, P = 0.022) and frequency of G-CSF administration (>20, P = 0.007) impacted the atherosclerotic lesion area changes. CONCLUSION: The meta-analysis suggested that G-CSF treatment might inhibit the progression of atherosclerosis in animal models.
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spelling pubmed-56133642017-11-14 The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis Liu, Manli Liu, Kejian Chen, Dongdong Chen, Hongzhi Sun, Kunming Ju, Xinxin Lan, Jiaojiao Zhou, Yang Wang, Weishan Pang, Lijuan Biomed Res Int Review Article BACKGROUND: Atherosclerosis is a common inflammatory disease. Stem cell and endothelial progenitor cell treatments can improve cardiac function after myocardial infarction. Granulocyte colony-stimulating factor (G-CSF) is a mobilisation agent, mobilising stem cells from the bone marrow to circulation in the blood. G-CSF may constitute a treatment of atherosclerosis. We have conducted meta-analysis to evaluate the current evidence for the effect of G-CSF on the progression of atherosclerosis in animal models and to provide reference for preclinical experiments and future human clinical trials of atherosclerosis treatment. METHODS: We searched several databases and conducted a meta-analysis across seven articles using a random-effect model. All statistical analyses were performed using Review Manager Version 5.2 and Stata 12.0. RESULTS: We found that G-CSF therapy was associated with reduced atherosclerotic lesion area (weighted mean difference (WMD): 7.29%; 95% confidence interval (CI): 2.06–12.52%; P = 0.006). No significant differences in total serum cholesterol (P = 0.54) and triglyceride levels (P = 0.95) were noted in G-CSF treatment groups compared with controls. Multivariable metaregression analysis revealed that the animal type (rabbit, P = 0.022) and frequency of G-CSF administration (>20, P = 0.007) impacted the atherosclerotic lesion area changes. CONCLUSION: The meta-analysis suggested that G-CSF treatment might inhibit the progression of atherosclerosis in animal models. Hindawi 2017 2017-09-12 /pmc/articles/PMC5613364/ /pubmed/29138752 http://dx.doi.org/10.1155/2017/6705363 Text en Copyright © 2017 Manli Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Liu, Manli
Liu, Kejian
Chen, Dongdong
Chen, Hongzhi
Sun, Kunming
Ju, Xinxin
Lan, Jiaojiao
Zhou, Yang
Wang, Weishan
Pang, Lijuan
The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title_full The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title_fullStr The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title_full_unstemmed The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title_short The Effect of Granulocyte Colony-Stimulating Factor on the Progression of Atherosclerosis in Animal Models: A Meta-Analysis
title_sort effect of granulocyte colony-stimulating factor on the progression of atherosclerosis in animal models: a meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613364/
https://www.ncbi.nlm.nih.gov/pubmed/29138752
http://dx.doi.org/10.1155/2017/6705363
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