Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials

Aim: This study was designed to systematically evaluate the effects of growth factor (GF) for therapeutic angiogenesis on ischemic heart disease (IHD) by pooling the results of randomized controlled trials (RCTs).Methods and Results: PubMed, EMBASE, and CENTRAL databases were searched from inception...

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Main Authors: Ling Tan, Lin-Zi Long, Hong-Zheng Li, Wen-Wen Yang, Yu-Xuan Peng, Jie-Ming Lu, Fei-Fei Liao, Xiao-Chang Ma, Hua Qu, Chang-Geng Fu, Shan-Shan Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2022.1095623/full
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author Ling Tan
Lin-Zi Long
Hong-Zheng Li
Hong-Zheng Li
Wen-Wen Yang
Yu-Xuan Peng
Yu-Xuan Peng
Jie-Ming Lu
Jie-Ming Lu
Fei-Fei Liao
Fei-Fei Liao
Xiao-Chang Ma
Xiao-Chang Ma
Hua Qu
Hua Qu
Chang-Geng Fu
Chang-Geng Fu
Shan-Shan Zhang
author_facet Ling Tan
Lin-Zi Long
Hong-Zheng Li
Hong-Zheng Li
Wen-Wen Yang
Yu-Xuan Peng
Yu-Xuan Peng
Jie-Ming Lu
Jie-Ming Lu
Fei-Fei Liao
Fei-Fei Liao
Xiao-Chang Ma
Xiao-Chang Ma
Hua Qu
Hua Qu
Chang-Geng Fu
Chang-Geng Fu
Shan-Shan Zhang
author_sort Ling Tan
collection DOAJ
description Aim: This study was designed to systematically evaluate the effects of growth factor (GF) for therapeutic angiogenesis on ischemic heart disease (IHD) by pooling the results of randomized controlled trials (RCTs).Methods and Results: PubMed, EMBASE, and CENTRAL databases were searched from inception to October 2022. RCTs, investigating the effects of GF therapy on IHD, were included. The risk bias of included study was assessed according to Cochrane tool. Weighted mean difference (WMD), calculated with fixed effect model or random effect model, was used to evaluate the effects of GF therapy on left ventricular ejection fraction (LVEF) and Canadian Cardiovascular Society (CCS) angina class. Relative risk (RR) was used to evaluate the effects of GF therapy on all-cause mortality, major adverse cardiovascular events (MACE) and revascularization. Meta-analysis, meta-regression analysis and publication bias analysis were performed by RevMan 5.3 or Stata 15.1 software. Twenty-nine studies involving 2899 IHD patients (1,577 patients in GF group and 1,322 patients in control group) were included. Compared with the control group, GF therapy did not reduce all-cause mortality (RR: 0.82; 95% CI: 0.54–1.24; p = 0.341), MACE [(RR: 0.83; 95% CI: 0.61–1.12; p = 0.227), revascularization (RR: 1.27, 95% CI: 0.82–1.96, p = 0.290) and CCS angina class (WMD: −0.08, 95% CI: −0.36 to 0.20, p = 0.560). However, GF therapy could increase LVEF during short-term follow-up (<1 year).Conclusion: GF for therapeutic angiogenesis was beneficial for increasing LVEF during short-term follow-up (<1 year), however, the therapy was not efficacious in decreasing all-cause mortality, MACE and revascularization.
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spelling doaj.art-b03ef2e8fb6743518a999ec6ab5a070d2022-12-22T04:22:09ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2022-12-011010.3389/fcell.2022.10956231095623Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trialsLing Tan0Lin-Zi Long1Hong-Zheng Li2Hong-Zheng Li3Wen-Wen Yang4Yu-Xuan Peng5Yu-Xuan Peng6Jie-Ming Lu7Jie-Ming Lu8Fei-Fei Liao9Fei-Fei Liao10Xiao-Chang Ma11Xiao-Chang Ma12Hua Qu13Hua Qu14Chang-Geng Fu15Chang-Geng Fu16Shan-Shan Zhang17Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaGraduate School of Beijing University of Chinese Medicine, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaGraduate School of Beijing University of Chinese Medicine, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaGraduate School of Beijing University of Chinese Medicine, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaGraduate School of Beijing University of Chinese Medicine, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaNational Cardiovascular Clinical Medical Research Center of TCM, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaNational Cardiovascular Clinical Medical Research Center of TCM, Beijing, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, ChinaNational Cardiovascular Clinical Medical Research Center of TCM, Beijing, ChinaBeijing Xibeiwang Town Community Health Service Center, Beijing, ChinaAim: This study was designed to systematically evaluate the effects of growth factor (GF) for therapeutic angiogenesis on ischemic heart disease (IHD) by pooling the results of randomized controlled trials (RCTs).Methods and Results: PubMed, EMBASE, and CENTRAL databases were searched from inception to October 2022. RCTs, investigating the effects of GF therapy on IHD, were included. The risk bias of included study was assessed according to Cochrane tool. Weighted mean difference (WMD), calculated with fixed effect model or random effect model, was used to evaluate the effects of GF therapy on left ventricular ejection fraction (LVEF) and Canadian Cardiovascular Society (CCS) angina class. Relative risk (RR) was used to evaluate the effects of GF therapy on all-cause mortality, major adverse cardiovascular events (MACE) and revascularization. Meta-analysis, meta-regression analysis and publication bias analysis were performed by RevMan 5.3 or Stata 15.1 software. Twenty-nine studies involving 2899 IHD patients (1,577 patients in GF group and 1,322 patients in control group) were included. Compared with the control group, GF therapy did not reduce all-cause mortality (RR: 0.82; 95% CI: 0.54–1.24; p = 0.341), MACE [(RR: 0.83; 95% CI: 0.61–1.12; p = 0.227), revascularization (RR: 1.27, 95% CI: 0.82–1.96, p = 0.290) and CCS angina class (WMD: −0.08, 95% CI: −0.36 to 0.20, p = 0.560). However, GF therapy could increase LVEF during short-term follow-up (<1 year).Conclusion: GF for therapeutic angiogenesis was beneficial for increasing LVEF during short-term follow-up (<1 year), however, the therapy was not efficacious in decreasing all-cause mortality, MACE and revascularization.https://www.frontiersin.org/articles/10.3389/fcell.2022.1095623/fullgrowth factortherapeutic angiogenesisischemic heart diseasemeta-analysisrandomized controlled study
spellingShingle Ling Tan
Lin-Zi Long
Hong-Zheng Li
Hong-Zheng Li
Wen-Wen Yang
Yu-Xuan Peng
Yu-Xuan Peng
Jie-Ming Lu
Jie-Ming Lu
Fei-Fei Liao
Fei-Fei Liao
Xiao-Chang Ma
Xiao-Chang Ma
Hua Qu
Hua Qu
Chang-Geng Fu
Chang-Geng Fu
Shan-Shan Zhang
Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
Frontiers in Cell and Developmental Biology
growth factor
therapeutic angiogenesis
ischemic heart disease
meta-analysis
randomized controlled study
title Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
title_full Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
title_fullStr Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
title_full_unstemmed Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
title_short Growth factor for therapeutic angiogenesis in ischemic heart disease: A meta-analysis of randomized controlled trials
title_sort growth factor for therapeutic angiogenesis in ischemic heart disease a meta analysis of randomized controlled trials
topic growth factor
therapeutic angiogenesis
ischemic heart disease
meta-analysis
randomized controlled study
url https://www.frontiersin.org/articles/10.3389/fcell.2022.1095623/full
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