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Effects of timing on intracoronary autologous bone marrow-derived cell transplantation in acute myocardial infarction: a meta-analysis of randomized controlled trials
Stem Cell Research & Therapy volume 8, Article number: 231 (2017)
Several cell-based therapies for adjunctive treatment of acute myocardial infarction have been investigated in multiple clinical trials, but the timing of transplantation remains controversial. We conducted a meta-analysis of randomized controlled trials to investigate the effects of timing on bone marrow-derived cell (BMC) therapy in acute myocardial infarction (AMI).
A systematic literature search of PubMed, MEDLINE, and Cochrane Evidence-Based Medicine databases from January 2000 to June 2017 was performed on randomized controlled trials with at least a 3-month follow-up for patients with AMI undergoing emergency percutaneous coronary intervention (PCI) and receiving intracoronary BMC transfer thereafter. The defined end points were left ventricular (LV) ejection fraction, LV end-diastolic and end-systolic index. The data were analyzed to evaluate the effects of timing on BMC therapy.
Thirty-four RCTs comprising a total of 2,307 patients were included; the results show that, compared to the control group, AMI patients who received BMC transplantation showed significantly improved cardiac function. BMC transplantation 3–7 days after PCI (+3.32%; 95% CI, 1.91 to 4.74; P < 0.00001) resulted in a significant increase of left ventricular ejection fraction (LVEF). As for the inhibitory effect on ventricular remodeling, BMC transplantation 3–7 days after PCI reduced LV end-diastolic indexes (–4.48; 95% CI, −7.98 to –0.98; P = 0.01) and LV end-systolic indexes (–6.73; 95% CI, –11.27 to –2.19; P = 0.004). However, in the groups who received BMC transplantation either within 24 hours or later than 7 days there was no significant effect on treatment outcome. In subgroup analysis, the group with LVEF ≤ 50% underwent a significant decrease in LV end-diastolic index after BMC transplantation (WMD = –3.29, 95% CI, –4.49 to –2.09; P < 0.00001); the decrease was even more remarkable in the LV end-systolic index after BMC transplantation in the group with LVEF ≤ 50% (WMD = –5.25, 95% CI, –9.30 to –1.20; P = 0.01), as well as in patients who received a dose of 10^7–10^8 cells (WMD = –12.99, 95% CI, –19.07 to –6.91; P < 0.0001). In the group with a follow-up of more than 12 months, this beneficial effect was significant and increased to a more pronounced effect of +3.58% (95% CI, 1.55 to 5.61; P = 0.0006) when compared with control.
In this meta-analysis, BMC transfer at 3 to 7 days post-AMI was superior to transfer within 24 hours or more than 7 days after AMI in improving LVEF and decreasing LV end-systolic dimensions or LV end-diastolic dimensions. It is more effective in patients with lower baseline LVEF (≤50%) and the effect can last more than 12 months.
With progress in intervention techniques and drug treatment, the mortality of acute myocardial infarction (AMI) has been significantly reduced. However, the incidence of heart failure after myocardial infarction remains high . Therefore, ways to restore heart function after myocardial infarction and to increase the long-term survival rate is the major research concern. Strauer et al.  performed autologous bone marrow-derived cell (BMC) transplantation on AMI patients for the first time, confirming the safety and effectiveness of stem cell transplantation. A quantity of basic and clinical studies on transplantation of BMCs in AMI treatment have produced mixed results as the subjects, the approach, the timing and the type and dose of transplanted stem cells varied. Existing meta-analyses of BMC transplantation in AMI focuses on the safety and effectiveness of BMC transplantation in AMI patients [3,4,5] and there have been few studies concerned with the specific approach used for BMC transplantation and evaluation.
Basic studies show that after AMI, increases in the expression of inflammatory chemokines and other cytokines might enhance the homing and differentiation of BMCs. In contrast, a strong inflammatory reaction often accompanies the release of reactive oxides and other cytokines at the site of infarction after AMI, which is detrimental to the survival and differentiation of autologous myocardial cells and transplanted BMCs [6, 7]. In addition, BMCs transplanted at different stages are affected by the microenvironment of myocardium. This may influence the survival and differentiation of transplanted BMCs, and may even cause their apoptosis [8, 9]. Therefore, the timing of BMC transplantation is considered to be one of the crucial factors affecting the survival of transplanted BMCs and hence the effectiveness of treatment.
A meta-analysis of different timings of intracoronary transplantation of BMCs in AMI patients was performed to study the effect of timing of stem cell transplantation on AMI treatment. Our research will provide a clue for the choice of optimal timing of BMC transplantation in AMI treatment.
Study source and selection
Literature on randomized controlled trials (RCTs) of autologous BMC treatment of AMI from January 2000 to June 2017 was retrieved from PubMed, MEDLINE and Cochrane databases. The subject terms or keywords used to retrieve the literature were “cell therapy, cell transplantation, stem cell therapy, bone marrow-derived cell, acute myocardial infarction”. Study selection was performed by two different researchers.
Studies were included that met the following criteria: (1) type of research: RCTs; follow-up duration: at least 3 months; (2) object of research: clinically diagnosed as AMI. The cases in the experimental group received percutaneous coronary intervention (PCI) and BMC transplantation. The cases in the control group did not receive bone marrow-derived stem cells (BMSCs) (e.g. control media or plasma); (3) intervention therapy: the cases in the experimental group received intracoronary transplantation of autologous BMCs, regardless of the type and dose of stem cells administered; (4) outcome indicators: primary indicators included left ventricular ejection fraction (LVEF), left ventricular end-diastolic volume (LVEDV) (or left ventricular end-diastolic volume index, LVEDVI) and left ventricular end-systolic volume (or left ventricular end-systolic volume index, LVESVI); secondary indicator was a cardiovascular adverse event; (5) publication in English or Chinese. The exclusion criteria were as follows: (1) intravenous injection or intramyocardial injection; (2) cytokine intervention or stem cell mobilization using cytokines; (3) lack of control group. Differences in researchers’ assessments of articles were resolved by a discussion with a third researcher.
Data extraction and analysis was performed by three independent researchers. For each study, we documented the articles and they were categorized into trial characteristics and functional outcome. Different assessments from data extraction were resolved by a discussion with a third researcher. Study information was recorded as follows: study design, baseline characteristics of included study, risk of bias of each study.
The quality of RCTs was assessed by The Cochrane Collaboration’s tool for assessing risk of bias (See Additional file 1: Figure S1).
A variety of stem cells included in this studies, such as bone marrow-derived cells, bone marrow stem cells, bone marrow mononuclear cells and bone marrow progenitor cell. BMCs were the main focus of this study because the majority of studies to date assessed this specific cell type. The outcome of LV function (e.g. LVEF), left ventricular end-diastolic index (e.g. LVEDV, LVEDVI), as well as left ventricular end-systolic index (e.g. LVESV and LVESVI) were the primary end points of our analysis, and mainly measured by cardiac magnetic resonance imaging (MRI), echocardiography, positron emission tomography-computed tomography (PET-CT) and single-photon emission computed tomography (SPECT).
The variations of left ventricular functional indexes in experimental and control groups compared with baselines were analyzed using Revman 5.3 software (The Cochrane Collaboration, Copenhagen, Denmark). We studied the difference in mean change (from baseline to follow-up) between patients who received stem cells and those who received control treatment. Most outcomes were reported as mean ± SD at baseline and follow-up. The mean change was then determined as follow-up to baseline, whereas SD change was determined as SEM (sample size). However, weighted mean difference (WMD) and standardized mean difference (SMD) were both expressed as a 95% confidence interval (CI).
The χ2 test was implemented to test the heterogeneity among the included trials: we considered that at P values ≤ 0.10, the trials could be considered heterogeneous. Therefore, trials that might give rise to heterogeneity were excluded and the reasons for such heterogeneity were identified. A funnel plot was drawn to evaluate possible bias. Subgroup analysis was performed to calculate summary statistics. If heterogeneity still existed after such treatment, the random effect model was employed to calculate summary statistics by the D-L method (DerSimonian and Laird method) . I2 was used to quantify the heterogeneity. If I2 > 50%, the heterogeneity was considered significant.
Subgroup analysis investigated the effect on summary statistics brought about by the timing of stem cell transplantation (within 24 hours or between 3 and 7 days or over 7 days), baseline LVEF (≤50% or > 50%), follow-up time(<6 months,< 12 months or ≥ 12 months) and dose of BMCs administered.
Preliminary retrieval obtained 1,401 papers, of which 1,196 were excluded by reading the title and abstract. The excluded papers were concerned with animal trials, comments, reviews and repeatedly reported trials. The remaining 205 papers were read thoroughly and 99 summaries or papers concerned with nonrandomized controlled trials were excluded. Another 77 papers were also excluded due to incomplete data, no setting up of a control group or use of a BMC injection method other than intracoronary injection. Finally, 29 articles were included in the meta-analysis, which reported 34 RCTs, comprising a total of 2,307 patients, 1,112 of whom were treated with an injection of cells (Fig. 1).
General information of included studies: after screening, 29 articles [11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39] were included in the meta-analysis, reporting data from a total of 34 RCTs comprising a total of 2,307 patients, 1.112 of whom were treated with cells. All of the included trials contained a control group and a BMC transplantation group. The average age of the patients was 55.7 ± 2.8 years, and male patients accounted for 84.6 ± 8.3%. Baseline LVEF was (44.7 ± 7.3%); intracoronary injection of autologous BMCs was performed using a dose of (7.17 ± 16.4) × 10^8 cells. Other information included the follow-up duration and the timing of BMC injection (Table 1).
In this analysis, 2,307 patients had a complete set of baseline and follow-up LVEF measurements (34 RCTs), 1,622 patients had complete left ventricular end-diastolic indexes measurements (26 RCTs) and 1,447 patients had complete left ventricular end-systolic indexes measurements (23 RCTs).
Effect of time window of BMC transplantation on left ventricular function
Meta-analysis of the included studies was conducted and summary statistics were calculated. The experimental groups and control groups which received stem cell transplantation within 1 day, 3–7 days and over 7 days after percutaneous coronary intervention were compared. Indicators were the variations of LVEF and left ventricular end-diastolic and end-systolic indexes compared with baselines, in the evaluation of the effect of stem cell transplantation on cardiac functions and on inhibition of left ventricular remodeling. The results of our analysis indicated that overall LVEF is increased by 2.02% (95% CI, 0.76 to 3.27; P = 0.02). The LVEF of the BMC transplantation group with a time window of 3–7 days was significantly increased by 3.32% (95% CI, 1.91 to 4.74; P < 0.00001) (Fig. 2). The forest plot shows that the unadjusted difference in the mean change in LVEDI with a time window of 3–7 days significantly decreased by 4.48 mL (95% CI, −7.98 to –0.98; P = 0.01) in the BMC group (Fig. 3). Further, LVESI with a time window of 3–7 days was significantly decreased by 6.73 mL (95% CI, −11.27 to −2.19; P = 0.002) in the treatment group (Fig. 4). These results showed much improved left ventricular functions in the BMC transplantation group with a time window of 3–7 days compared with the groups with time windows of up to 24 hours or over 7 days.
Left ventricular function was significantly improved in the BMC transplantation group with a time window of 3–7 days. However, significant heterogeneity (I2 > 50%) still existed among the studies. Therefore, subgroup analysis was conducted of the baseline LVEF values and the follow-up period used, which were possible sources of heterogeneity. The trials were divided into groups as follows: baseline LVEF values > 50% and ≤ 50%; duration of follow-up < 6 months, < 12 months and ≥ 12 months; and cell doses of ≤ 10^7, ≤ 10^8, ≤ 10^9 or ≤ 10^10 BMCs.
Effect of baseline LVEF before BMC transplantation on left ventricular function
The group with LVEF ≤ 50% (18 RCTs) underwent a significant decrease in LV end-diastolic index after BMC transplantation (WMD = –3.29, 95% CI, –4.49 to –2.09, P < 0.00001); the decrease in LVESI after BMC transplantation was even more remarkable in this group (15 RCTs) (WMD = –5.25, 95% CI, –9.30 to –1.20, P = 0.01, Table 2). However in both groups, baseline LVEF did not have a significant effect on treatment outcome in terms of LV ejection fraction. According to our data, patients with a higher LVEF (>50%) at baseline did not benefit more from cell therapy compared with patients with lower LVEF (≤50%).
Effect of follow-up period after BMC transplantation on left ventricular function
Subgroup analysis revealed that in patients with follow up periods of < 6 months (7 RCTs), LVEF increased by 1.45% (95% CI, 0.54 to 2.36; P = 0.002, Table 3). In the group with a follow-up period of ≥ 12 month (14 RCTs), this beneficial effect was significant and increased to a more pronounced effect of 3.58% (95% CI, 1.55 to 5.61; P = 0.0006, Table 3) when compared with controls. Both the group with a follow-up duration of < 6 months and that with follow-up of ≥ 12 months underwent a significant decrease in LVEDI after BMC transplantation (WMD = –4.76, 95% CI, –8.19 to –1.33; P = 0.006; WMD = –4.00, 95% CI, –8.13 to 0.13; P = 0.06, Table 3); the decrease in LVESI was more sustained in the group with a follow-up duration of ≥12 months (WMD = –7.07, 95% CI, –11.99 to–2.14; P = 0.005, Table 3). These data demonstrate that cell transplantation in patients with AMI can result in an improvement which is not only short-term, and that this effect can last more than 12 months.
Effect of cell dose used for BMC transplantation on left ventricular function
Intracoronary infusion of BMCs (cell dose of ≤ 10^8) resulted in a significant decrease in LVEDI by 7.36 mL (95% CI, –11.45 to–3.27; P = 0.0004, Table 4), whereas BMC transplantation resulted in a decrease in LVESI by 12.99 mL (95% CI, –19.07 to –6.91; P < 0.0001, Table 4). LVEF increased by 1.56% after transplantation of BMCs (95% CI, –2.95 to 6.06; P = NS; Table 4). Subgroup analysis revealed the tendency that the effect of BMC transplantation maybe better in patients who received a dose of 10^7–10^8 bone marrow cells.
The safety of BMC transplantation is also important at the moment. We chose death and reinfarction of the patients. Our study found that the stem cells transplantation had not too much influence on mortality and reinfarction (Fig. 5).
Sensitivity analysis and publication bias
Sensitivity analysis is a method of evaluating the stability and reliability of meta-analyses. By getting rid of each trial one by one, the sensitivity analysis evaluates the stability of the WMD of LVEF and is used to observe whether summary statistics change. A funnel plot of LVEF values showed that studies were equally distributed around the overall estimate, suggesting that there was no evidence of publication bias (Fig. 6).
In this meta-analysis, which comprises a total of 2,307 patients with AMI, cell therapy proved to be safe. Previous meta-analyses on autologous BMC transplantation in AMI patients were mostly concerned with the security and effectiveness of such a technique. Therefore, the present research placed a greater emphasis on the effect of timing of stem cell transplantation and the choice of optimal time window.
Our study showed that compared to the control group, AMI patients demonstrated significantly improved cardiac function after receiving BMC transplantation. BMC transplantation 3–7 days after AMI resulted in a significant increase of LVEF. As for the inhibitory effect against ventricular remodeling, BMC transplantation 3–7 days after PCI reduced LVEDI and LVESI. However, in both the group who underwent transplantation within 24 hours and those who underwent transplantation at over 7 days, no significant effect was observed on treatment outcome. The statistics showed much improved left ventricular function in the BMC transplantation group with a time window of 3–7 days compared to those with a time window of < 24 hours or over 7 days. This result showed that inflammation may influence the bone marrow-derived cells to settle and differentiate in the early phase (within 24 hours) of acute myocardial infarction; when BMC transplantation occurs over 7 days after PCI, the fibroblasts present and the mechanical traction exerted by scar tissue during this period also have an impact on the ability of BMCs to differentiate. Consequently, choosing the right time to perform the transplantation not only directly relates to the survival of the stem cells, but also relates to the biological effects of the stem cells, and thus to the improvement in cardiac function.
Subgroup analysis found that the effect of BMC transplantation LVEF has no difference in the 10^7-10^8 bone marrow cells, but LVEDVI and LVESVI show a clearly improve in the 10^7-10^8 range. Some studies found that 10^8 is the lowest cell number to achieve favorable effects on LV function [40,41,42]. However, Wang et al. showed that the injection of no more than 10^7 MSCs for AMI after percutaneous coronary intervention might improve left ventricular systolic function . So we need more research to clarify which dosage is better.
At the same time, our study demonstrates that cell transplantation in patients with AMI can result in a significant elevation of LVEF after a follow-up duration of both < 6 month and > 12 month, but not at < 12 month. This may associate with the incidence of adverse events, the inflammatory response, or time of stem cell differentiation and so on. So further study is needed to clarify this.
According to our data, baseline LVEF, dose of BMCs used and duration of follow-up might all influence the effectiveness of BMC treatment. Experiments by Janssens et al.  and Tendera et al.  found that the effect of BMC transplantation was more apparent in patients with low LVEF. However, the recent HBEB  and BONAMI studies  with a large sample size found that cardiac function of patients after a larger area of AMI or lower baseline LVEF (≤45%) were not significantly improved after BMC transplantation compared to the control group (38.6% ± 24.7% vs. 42.4% ± 18.7%; P = 0.33). Our research showed that the improvement was more significant in patients whose baseline LVEF values were ≤ 50%.
Regarding the dose of BMCs administered, it is believed that the dose correlates positively with the improvement in cardiac function, i.e., the greater the number of bone marrow-derived cells reaching the ischemic and infarct zone, the greater the effectiveness will be. However, due to differences in the animal models used, type of transplanted cells, and cell isolation and purification techniques between different studies, the dose of cells administered varied greatly from one study to another. A large number of studies were devoted to dose dependency. Iwasaki et al.  found that the function of myocardium and angiogenesis in mice was dose-dependent when CD34+ cells were injected to infarcted myocardium. These findings indicate that transplantation of a higher dose of cells is more effective than low doses in the treatment of damaged myocardium. Our study also showed that the effectiveness of BMC transplantation was better in patients who received a dose of 10^7–10^8 bone marrow cells.
The first clinical long-term studies showed a gradually increasing functional benefit of cell transplantation within the first post-transplant year . In contrast, Meluzín et al.  found that autologous mononuclear bone marrow cell transplantation could significantly improve left ventricular systolic function after AMI, but benefit of cell transplantation was partially lost during the 12-month follow-up. In this meta-analysis we found that cell transplantation in patients with AMI can not only provide short-term improvement, but that this effect can last more than 12 months.
Although the results proved the effectiveness of BMC transplantation in treatment of AMI by meta-analysis of randomized controlled trials involving a large number of subjects, and no publication bias was found, the present study also had its limitations. Currently, the individual patient data (IPD) meta-analysis is the gold standard for meta-analyses; it can assess the impact of a treatment on clinical outcomes, especially in the case of small and medium-sized clinical studies. The IPD database is kept simple; therefore, a meta-analysis cannot evaluate some surrogate parameters if data are not gathered or factors are not available, such as different quality of life assessment scores.
Heterogeneity was quite apparent among included trials, and might arise from the non-homogeneity in the baseline indicators of subjects, dose of cells used for stem cell transplantation, timing of stem cell transplantation, the choice of placebo for the control groups, and measurement and outcome indicators. In addition, the duration of the follow-up period differed between different trials; some trials involved a medium-term or long-term follow-up. This might result in uncertainty of the long-term effectiveness of BMC transplantation. Therefore, more basic and clinical studies are required to examine the possible mechanisms of BMC transplantation in treating AMI and to standardize the approach to BMC transplantation.
The difficulties of the standard meta-analysis approaches have been reviewed here. Each has a place in the analysis of data when pivotal clinical trials are not available and each sheds light on the magnitude of the treatment effect in a complex health-care field.
In conclusion, meta-analysis of 29 papers reporting the results of 33 randomized controlled trials confirmed that BMC transplantation could significantly improve cardiac function after AMI, and that it could also increase LVEF and prevent ventricular remodeling. BMC transplantation 3–7 days after PCI was more effective than that within 24 hours or at over 7 days. Subgroup analysis indicated that BMC transplantation was more effective in patients with lower baseline LVEF values when cells were administered at a dose of 10^7–10^8 BMCs, and that this effect could last more than 12 months.
Acute myocardial infarction
Bone marrow-derived cell
individual patient data
Left ventricular end-diastolic volume
Left ventricular end-diastolic volume index
Left ventricular ejection fraction
Left ventricular end- systolic volume
Left ventricular end- systolic volume index
Magnetic resonance imaging
Percutaneous coronary intervention
Positron emission tomography-computed tomography
Randomized controlled trials
Standardized mean difference
Single-photon emission computed tomography
Weighted mean difference
Gajarsa JJ, Kloner RA. Left ventricular remodeling in the post-infarction heart: a review of cellular, molecular mechanisms, and therapeutic modalities. Heart Fail Rev. 2011;16(1):13–21.
Strauer BE, Brehm M, Zeus T, Gattermann N, Hernandez A, Sorg RV, Kogler G, Wernet P. Intracoronary, human autologous stem cell transplantation for myocardial regeneration following myocardial infarction. Deutsche Medizinische Wochenschrift (1946). 2001;126(34-35):932–8.
Abdel-Latif A, Bolli R, Tleyjeh IM, Montori VM, Perin EC, Hornung CA, Zuba-Surma EK, Al-Mallah M, Dawn B. Adult bone marrow-derived cells for cardiac repair: a systematic review and meta-analysis. Arch Intern Med. 2007;167(10):989–97.
Martin-Rendon E, Brunskill SJ, Hyde CJ, Stanworth SJ, Mathur A, Watt SM. Autologous bone marrow stem cells to treat acute myocardial infarction: a systematic review. Eur Heart J. 2008;29(15):1807–18.
Bai Y, Sun T, Ye P. Age, gender and diabetic status are associated with effects of bone marrow cell therapy on recovery of left ventricular function after acute myocardial infarction: a systematic review and meta-analysis. Ageing Res Rev. 2010;9(4):418–23.
Frangogiannis NG, Smith CW, Entman ML. The inflammatory response in myocardial infarction. Cardiovasc Res. 2002;53(1):31–47.
Frangogiannis NG. Targeting the inflammatory response in healing myocardial infarcts. Curr Med Chem. 2006;13(16):1877–93.
Pannitteri G, Petrucci E, Testa U. Coordinate release of angiogenic growth factors after acute myocardial infarction: evidence of a two-wave production. J Cardiovasc Med (Hagerstown). 2006;7(12):872–9.
Wojakowski W, Tendera M, Zebzda A, Michalowska A, Majka M, Kucia M, Maslankiewicz K, Wyderka R, Krol M, Ochala A, et al. Mobilization of CD34(+), CD117(+), CXCR4(+), c-met(+) stem cells is correlated with left ventricular ejection fraction and plasma NT-proBNP levels in patients with acute myocardial infarction. Eur Heart J. 2006;27(3):283–9.
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.
Janssens S, Dubois C, Bogaert J, Theunissen K, Deroose C, Desmet W, Kalantzi M, Herbots L, Sinnaeve P, Dens J, et al. Autologous bone marrow-derived stem-cell transfer in patients with ST-segment elevation myocardial infarction: double-blind, randomised controlled trial. Lancet (London, England). 2006;367(9505):113–21.
Yousef M, Schannwell CM, Kostering M, Zeus T, Brehm M, Strauer BE. The BALANCE Study: clinical benefit and long-term outcome after intracoronary autologous bone marrow cell transplantation in patients with acute myocardial infarction. J Am Coll Cardiol. 2009;53(24):2262–9.
Wang X, Xi WC, Wang F. The beneficial effects of intracoronary autologous bone marrow stem cell transfer as an adjunct to percutaneous coronary intervention in patients with acute myocardial infarction. Biotechnol Lett. 2014;36(11):2163–8.
Piepoli MF, Vallisa D, Arbasi M, Cavanna L, Cerri L, Mori M, Passerini F, Tommasi L, Rossi A, Capucci A. Bone marrow cell transplantation improves cardiac, autonomic, and functional indexes in acute anterior myocardial infarction patients (Cardiac Study). Eur J Heart Fail. 2010;12(2):172–80.
Panovsky R, Meluzin J, Janousek S, Mayer J, Kaminek M, Groch L, Prasek J, Stanicek J, Dusek L, Hlinomaz O, et al. Cell therapy in patients with left ventricular dysfunction due to myocardial infarction. Echocardiography (Mount Kisco, NY). 2008;25(8):888–97.
Gao LR, Pei XT, Ding QA, Chen Y, Zhang NK, Chen HY, Wang ZG, Wang YF, Zhu ZM, Li TC, et al. A critical challenge: dosage-related efficacy and acute complication intracoronary injection of autologous bone marrow mesenchymal stem cells in acute myocardial infarction. Int J Cardiol. 2013;168(4):3191–9.
Sürder D, Manka R, Moccetti T, Lo Cicero V, Emmert MY, Klersy C, Soncin S, Turchetto L, Radrizzani M, Zuber M, et al. Effect of bone marrow-derived mononuclear cell treatment, early or late after acute myocardial infarction: twelve months CMR and long-term clinical results. Circ Res. 2016;119(3):481–90.
Traverse JH, Henry TD, Ellis SG, Pepine CJ, Willerson JT, Zhao DX, Forder JR, Byrne BJ, Hatzopoulos AK, Penn MS, et al. Effect of intracoronary delivery of autologous bone marrow mononuclear cells 2 to 3 weeks following acute myocardial infarction on left ventricular function: the LateTIME randomized trial. JAMA. 2011;306(19):2110–9.
Plewka M, Krzeminska-Pakula M, Lipiec P, Peruga JZ, Jezewski T, Kidawa M, Wierzbowska-Drabik K, Korycka A, Robak T, Kasprzak JD. Effect of intracoronary injection of mononuclear bone marrow stem cells on left ventricular function in patients with acute myocardial infarction. Am J Cardiol. 2009;104(10):1336–42.
Traverse JH, Henry TD, Pepine CJ, Willerson JT, Zhao DX, Ellis SG, Forder JR, Anderson RD, Hatzopoulos AK, Penn MS, et al. Effect of the use and timing of bone marrow mononuclear cell delivery on left ventricular function after acute myocardial infarction: the TIME randomized trial. JAMA. 2012;308(22):2380–9.
Chen SL, Fang WW, Ye F, Liu YH, Qian J, Shan SJ, Zhang JJ, Chunhua RZ, Liao LM, Lin S, et al. Effect on left ventricular function of intracoronary transplantation of autologous bone marrow mesenchymal stem cell in patients with acute myocardial infarction. Am J Cardiol. 2004;94(1):92–5.
Ge J, Li Y, Qian J, Shi J, Wang Q, Niu Y, Fan B, Liu X, Zhang S, Sun A, et al. Efficacy of emergent transcatheter transplantation of stem cells for treatment of acute myocardial infarction (TCT-STAMI). Heart. 2006;92(12):1764–7.
Wöhrle J, von Scheidt F, Schauwecker P, Wiesneth M, Markovic S, Schrezenmeier H, Hombach V, Rottbauer W, Bernhardt P. Impact of cell number and microvascular obstruction in patients with bone-marrow derived cell therapy: final results from the randomized, double-blind, placebo controlled intracoronary Stem Cell therapy in patients with Acute Myocardial Infarction (SCAMI) trial. Clin Res Cardiol. 2013;102(10):765–70.
Herbots L, D’Hooge J, Eroglu E, Thijs D, Ganame J, Claus P, Dubois C, Theunissen K, Bogaert J, Dens J, et al. Improved regional function after autologous bone marrow-derived stem cell transfer in patients with acute myocardial infarction: a randomized, double-blind strain rate imaging study. Eur Heart J. 2009;30(6):662–70.
Grajek S, Popiel M, Gil L, Breborowicz P, Lesiak M, Czepczynski R, Sawinski K, Straburzynska-Migaj E, Araszkiewicz A, Czyz A, et al. Influence of bone marrow stem cells on left ventricle perfusion and ejection fraction in patients with acute myocardial infarction of anterior wall: randomized clinical trial: impact of bone marrow stem cell intracoronary infusion on improvement of microcirculation. Eur Heart J. 2010;31(6):691–702.
Dill T, Schachinger V, Rolf A, Mollmann S, Thiele H, Tillmanns H, Assmus B, Dimmeler S, Zeiher AM, Hamm C. Intracoronary administration of bone marrow-derived progenitor cells improves left ventricular function in patients at risk for adverse remodeling after acute ST-segment elevation myocardial infarction: results of the Reinfusion of Enriched Progenitor cells And Infarct Remodeling in Acute Myocardial Infarction study (REPAIR-AMI) cardiac magnetic resonance imaging substudy. Am Heart J. 2009;157(3):541–7.
Wollert KC, Meyer GP, Lotz J, Ringes-Lichtenberg S, Lippolt P, Breidenbach C, Fichtner S, Korte T, Hornig B, Messinger D, et al. Intracoronary autologous bone-marrow cell transfer after myocardial infarction: the BOOST randomised controlled clinical trial. Lancet (London, England). 2004;364(9429):141–8.
Roncalli J, Mouquet F, Piot C, Trochu JN, Le Corvoisier P, Neuder Y, Le Tourneau T, Agostini D, Gaxotte V, Sportouch C, et al. Intracoronary autologous mononucleated bone marrow cell infusion for acute myocardial infarction: results of the randomized multicenter BONAMI trial. Eur Heart J. 2011;32(14):1748–57.
Meyer GP, Wollert KC, Lotz J, Pirr J, Rager U, Lippolt P, Hahn A, Fichtner S, Schaefer A, Arseniev L, et al. Intracoronary bone marrow cell transfer after myocardial infarction: 5-year follow-up from the randomized-controlled BOOST trial. Eur Heart J. 2009;30(24):2978–84.
Schächinger V, Erbs S, Elsasser A, Haberbosch W, Hambrecht R, Holschermann H, Yu J, Corti R, Mathey DG, Hamm CW, et al. Intracoronary bone marrow-derived progenitor cells in acute myocardial infarction. N Engl J Med. 2006;355(12):1210–21.
Bartunek J, Vanderheyden M, Vandekerckhove B, Mansour S, De Bruyne B, De Bondt P, Van Haute I, Lootens N, Heyndrickx G, Wijns W. Intracoronary injection of CD133-positive enriched bone marrow progenitor cells promotes cardiac recovery after recent myocardial infarction: feasibility and safety. Circulation. 2005;112(9 Suppl):I178–83.
Lunde K, Solheim S, Aakhus S, Arnesen H, Abdelnoor M, Egeland T, Endresen K, Ilebekk A, Mangschau A, Fjeld JG, et al. Intracoronary injection of mononuclear bone marrow cells in acute myocardial infarction. N Engl J Med. 2006;355(12):1199–209.
Beitnes JO, Gjesdal O, Lunde K, Solheim S, Edvardsen T, Arnesen H, Forfang K, Aakhus S. Left ventricular systolic and diastolic function improve after acute myocardial infarction treated with acute percutaneous coronary intervention, but are not influenced by intracoronary injection of autologous mononuclear bone marrow cells: a 3 year serial echocardiographic sub-study of the randomized-controlled ASTAMI study. Eur J Echocardiogr. 2011;12(2):98–106.
Huang RC, Yao K, Zou YZ, Ge L, Qian JY, Yang J, Yang S, Niu YH, Li YL, Zhang YQ, et al. Long term follow-up on emergent intracoronary autologous bone marrow mononuclear cell transplantation for acute inferior-wall myocardial infarction. Zhonghua yi xue za zhi. 2006;86(16):1107–10.
Cao F, Sun D, Li C, Narsinh K, Zhao L, Li X, Feng X, Zhang J, Duan Y, Wang J, et al. Long-term myocardial functional improvement after autologous bone marrow mononuclear cells transplantation in patients with ST-segment elevation myocardial infarction: 4 years follow-up. Eur Heart J. 2009;30(16):1986–94.
Hopp E, Lunde K, Solheim S, Aakhus S, Arnesen H, Forfang K, Edvardsen T, Smith HJ. Regional myocardial function after intracoronary bone marrow cell injection in reperfused anterior wall infarction - a cardiovascular magnetic resonance tagging study. J Cardiovasc Magn Reson. 2011;13:22.
Yao K, Huang R, Sun A, Qian J, Liu X, Ge L, Zhang Y, Zhang S, Niu Y, Wang Q, et al. Repeated autologous bone marrow mononuclear cell therapy in patients with large myocardial infarction. Eur J Heart Fail. 2009;11(7):691–8.
Meluzín J, Janousek S, Mayer J, Groch L, Hornacek I, Hlinomaz O, Kala P, Panovsky R, Prasek J, Kaminek M, et al. Three-, 6-, and 12-month results of autologous transplantation of mononuclear bone marrow cells in patients with acute myocardial infarction. Int J Cardiol. 2008;128(2):185–92.
Wollert KC, Meyer GP, Muller-Ehmsen J, Tschope C, Bonarjee V, Larsen AI, May AE, Empen K, Chorianopoulos E, Tebbe U, et al. Intracoronary autologous bone marrow cell transfer after myocardial infarction: the BOOST-2 randomised placebo-controlled clinical trial. Eur Heart J. 2017. doi:10.1093/eurheartj/ehx188.
Clifford DM, Fisher SA, Brunskill SJ, Doree C, Mathur A, Clarke MJ, Watt SM, Martin-Rendon E. Long-term effects of autologous bone marrow stem cell treatment in acute myocardial infarction: factors that may influence outcomes. PLoS One. 2012;7(5), e37373.
Miettinen JA, Ylitalo KV, Niemela M, Kervinen K, Saily M, Koistinen P, Savolainen ER, Makikallio TH, Huikuri HV. Left ventricular functional recovery after intracoronary injection of autologous bone marrow-derived stem cells in patients with acute myocardial infarction: a dose-response pilot study. Int J Cardiol. 2012;154(3):354–6.
Xu JY, Cai WY, Tian M, Liu D, Huang RC. Stem cell transplantation dose in patients with acute myocardial infarction: a meta-analysis. Chronic Diseases and Translational Medicine. 2016;2:92–101.
Wang Z, Wang L, Su X, Pu J, Jiang M, He B. Rational transplant timing and dose of mesenchymal stromal cells in patients with acute myocardial infarction: a meta-analysis of randomized controlled trials. Stem Cell Res Ther. 2017;8(1):21.
Tendera M, Wojakowski W, Ruzyllo W, Chojnowska L, Kepka C, Tracz W, Musialek P, Piwowarska W, Nessler J, Buszman P, et al. Intracoronary infusion of bone marrow-derived selected CD34 + CXCR4+ cells and non-selected mononuclear cells in patients with acute STEMI and reduced left ventricular ejection fraction: results of randomized, multicentre Myocardial Regeneration by Intracoronary Infusion of Selected Population of Stem Cells in Acute Myocardial Infarction (REGENT) Trial. Eur Heart J. 2009;30(11):1313–21.
Hirsch A, Nijveldt R, van der Vleuten PA, Tijssen JG, van der Giessen WJ, Tio RA, Waltenberger J, ten Berg JM, Doevendans PA, Aengevaeren WR, et al. Intracoronary infusion of mononuclear cells from bone marrow or peripheral blood compared with standard therapy in patients after acute myocardial infarction treated by primary percutaneous coronary intervention: results of the randomized controlled HEBE trial. Eur Heart J. 2011;32(14):1736–47.
Iwasaki H, Kawamoto A, Ishikawa M, Oyamada A, Nakamori S, Nishimura H, Sadamoto K, Horii M, Matsumoto T, Murasawa S, et al. Dose-dependent contribution of CD34-positive cell transplantation to concurrent vasculogenesis and cardiomyogenesis for functional regenerative recovery after myocardial infarction. Circulation. 2006;113(10):1311–25.
Schachinger V, Assmus B, Britten MB, Honold J, Lehmann R, Teupe C, Abolmaali ND, Vogl TJ, Hofmann WK, Martin H, et al. Transplantation of progenitor cells and regeneration enhancement in acute myocardial infarction: final one-year results of the TOPCARE-AMI Trial. J Am Coll Cardiol. 2004;44(8):1690–9.
The authors greatly appreciate the work of revising by Aaron L. Leppin, Knowledge and Evaluation Research Unit, Mayo Clinic, Rochester, MN, USA. This work was supported by National Natural Science Foundation of China (81100220); The Specialized Research Fund for the Doctoral Program of Higher Education (20102105120005); Liaoning Province Department of Education Key Laboratory Project (2008S071) (China) and Liaoning Provincial Department of Education Fund (2009A192).
This work was supported by National Natural Science Foundation of China (81100220); The Specialized Research Fund for the Doctoral Program of Higher Education (20102105120005); Liaoning Province Department of Education Key Laboratory Project (2008S071) (China); and Liaoning Provincial Department of Education Fund (2009A192).
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Xu, Jy., Liu, D., Zhong, Y. et al. Effects of timing on intracoronary autologous bone marrow-derived cell transplantation in acute myocardial infarction: a meta-analysis of randomized controlled trials. Stem Cell Res Ther 8, 231 (2017). https://doi.org/10.1186/s13287-017-0680-5
- Acute myocardial infarction (AMI)
- Cell therapy
- Bone marrow-derived cells (BMCs)