Literature DB >> 22065869

Short- and long-term outcomes of intracoronary and endogenously mobilized bone marrow stem cells in the treatment of ST-segment elevation myocardial infarction: a meta-analysis of randomized control trials.

Hendrik Zimmet1, Pramote Porapakkham, Pornwalee Porapakkham, Yusuke Sata, Steven Joseph Haas, Silviu Itescu, Andrew Forbes, Henry Krum.   

Abstract

AIMS: Bone marrow stem cell (BMSC) treatment of ST-segment elevation myocardial infarction (STEMI) has been primarily via the intracoronary route or via endogenous mobilization using granulocyte colony-stimulating factor (G-CSF). Studies have provided conflicting results. We therefore performed a meta-analysis of these treatments, examining short- and long-term efficacy and safety. METHODS AND
RESULTS: Randomized controlled trials (RCTs) of BMSC-based therapy for STEMI, delivered within 9 days of reperfusion, were identified by systematic search. Random effects models were used to calculate pooled effects of clinical outcomes, with meta-regression to assess dependence of the magnitude of effect sizes on study characteristics. Twenty-nine RCTs enrolling 1830 patients were included. Intracoronary BMSC therapy resulted in an overall improvement in left ventricular ejection fraction (LVEF) of 2.70% [95% confidence interval (CI) 1.48-3.92; P < 0.001] in the short term and 3.31% (95% CI 1.87-4.75; P < 0.001) longer term. Meta-regression suggested a dose-response relationship between quantity of CD34(+) cells delivered and increase in LVEF (P = 0.007). G-CSF treatment resulted in a trend towards similar benefits (P = 0.20). No significant differences were observed in pooled adverse outcome rates between intervention and control groups of either treatment approach, except for lower revascularization rates with intracoronary BMSC vs. control (odds ratio 0.68, 95% CI 0.47-0.97; P = 0.03).
CONCLUSIONS: Intracoronary BMSC therapy post-STEMI improves LVEF beyond standard medical treatment, in both the short and longer term. G-CSF treatment shows positive but non-significant trends. Both treatments demonstrate safety comparable with conventional medical treatment.

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Year:  2011        PMID: 22065869     DOI: 10.1093/eurjhf/hfr148

Source DB:  PubMed          Journal:  Eur J Heart Fail        ISSN: 1388-9842            Impact factor:   15.534


  41 in total

1.  Intravenous administration of atorvastatin-pretreated mesenchymal stem cells improves cardiac performance after acute myocardial infarction: role of CXCR4.

Authors:  Na Li; Yue-Jin Yang; Hai-Yan Qian; Qing Li; Qian Zhang; Xiang-Dong Li; Qiu-Ting Dong; Hui Xu; Lei Song; Hao Zhang
Journal:  Am J Transl Res       Date:  2015-06-15       Impact factor: 4.060

2.  Peroxisome Proliferator-Activated Receptor Gamma Promotes Mesenchymal Stem Cells to Express Connexin43 via the Inhibition of TGF-β1/Smads Signaling in a Rat Model of Myocardial Infarction.

Authors:  Jingying Hou; Lingyun Wang; Jinghui Hou; Tianzhu Guo; Yue Xing; Shaoxin Zheng; Changqing Zhou; Hui Huang; Huibao Long; Tingting Zhong; Quanhua Wu; Jingfeng Wang; Tong Wang
Journal:  Stem Cell Rev Rep       Date:  2015-12       Impact factor: 5.739

Review 3.  Impact of intracoronary bone marrow cell therapy on left ventricular function in the setting of ST-segment elevation myocardial infarction: a collaborative meta-analysis.

Authors:  Ronak Delewi; Alexander Hirsch; Jan G Tijssen; Volker Schächinger; Wojciech Wojakowski; Jérôme Roncalli; Svend Aakhus; Sandra Erbs; Birgit Assmus; Michal Tendera; R Goekmen Turan; Roberto Corti; Tim Henry; Patricia Lemarchand; Ketil Lunde; Feng Cao; Heikki V Huikuri; Daniel Sürder; Robert D Simari; Stefan Janssens; Kai C Wollert; Michal Plewka; Stefan Grajek; Jay H Traverse; Felix Zijlstra; Jan J Piek
Journal:  Eur Heart J       Date:  2013-09-11       Impact factor: 29.983

4.  In-vivo comparison of the acute retention of stem cell derivatives and fibroblasts after intramyocardial transplantation in the mouse model.

Authors:  Cajetan Lang; Sebastian Lehner; Andrei Todica; Guido Boening; Mathias Zacherl; Wolfgang-Michael Franz; Bernd Joachim Krause; Peter Bartenstein; Marcus Hacker; Robert David
Journal:  Eur J Nucl Med Mol Imaging       Date:  2014-07-26       Impact factor: 9.236

5.  Adipose-derived mesenchymal stem cells embedded in platelet-rich fibrin scaffolds promote angiogenesis, preserve heart function, and reduce left ventricular remodeling in rat acute myocardial infarction.

Authors:  Yung-Lung Chen; Cheuk-Kwan Sun; Tzu-Hsien Tsai; Li-Teh Chang; Steve Leu; Yen-Yi Zhen; Jiunn-Jye Sheu; Sarah Chua; Kuo-Ho Yeh; Hung-I Lu; Hsueh-Wen Chang; Fan-Yen Lee; Hon-Kan Yip
Journal:  Am J Transl Res       Date:  2015-05-15       Impact factor: 4.060

Review 6.  Left ventricular ejection fraction as therapeutic target: is it the ideal marker?

Authors:  V Katsi; G Georgiopoulos; A Laina; E Koutli; J Parissis; C Tsioufis; P Nihoyannopoulos; D Tousoulis
Journal:  Heart Fail Rev       Date:  2017-11       Impact factor: 4.214

Review 7.  Bioengineered tissue solutions for repair, correction and reconstruction in cardiovascular surgery.

Authors:  Laura Iop; Tiziana Palmosi; Eleonora Dal Sasso; Gino Gerosa
Journal:  J Thorac Dis       Date:  2018-07       Impact factor: 2.895

8.  Optimized processing of growth factor mobilized peripheral blood CD34+ products by counterflow centrifugal elutriation.

Authors:  Chy-Anh Tran; Monica Torres-Coronado; Agnes Gardner; Angel Gu; Hieu Vu; Anitha Rao; Lan-Feng Cao; Amira Ahmed; David Digiusto
Journal:  Stem Cells Transl Med       Date:  2012-05-08       Impact factor: 6.940

Review 9.  Stem cell therapy to treat heart ischaemia: implications for diabetes cardiovascular complications.

Authors:  Abbas Ali Qayyum; Anders Bruun Mathiasen; Jens Kastrup
Journal:  Curr Diab Rep       Date:  2014-12       Impact factor: 4.810

Review 10.  Myocardial regeneration of the failing heart.

Authors:  Alexander T Akhmedov; José Marín-García
Journal:  Heart Fail Rev       Date:  2013-11       Impact factor: 4.214

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