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Efficacy and safety of bone marrow cell transplantation for chronic ischemic heart disease: a meta-analysis
Chun Xiao1, Shijie Zhou1, Yueqiang Liu1
1Department of Medicine, Sichuan Scientific & Cellular Biotechnology Research Institute, Chengdu, China (mainland).
Insights
Bone marrow-derived cell (BMC) therapy is safe and effective for chronic ischemic heart disease (CIHD) patients, improving heart function. Further large trials are needed to confirm long-term benefits of BMCs for heart repair.
Area of Science:
- Regenerative Medicine
- Cardiovascular Research
- Cell Therapy
Background:
- Bone marrow-derived cells (BMCs) show therapeutic promise for chronic ischemic heart disease (CIHD).
- The precise efficacy and safety of BMC therapy in CIHD patients remain incompletely defined.
Purpose of the Study:
- To conduct a meta-analysis evaluating the efficacy and safety of BMC transplantation in patients with CIHD.
- To assess the impact of BMC therapy on cardiac function and adverse events.
Main Methods:
- A systematic search of major databases (PubMed, OVID, EMBASE, Cochrane, ClinicalTrials.gov) identified 20 relevant trials.
- Efficacy assessed by changes in left ventricular ejection fraction (LVEF), left ventricular end-systolic volume (LVESV), and left ventricular end-diastolic volume (LVEDV).
- Safety evaluated through pooled data on all-cause death, ventricular arrhythmia, myocardial infarction, and cerebrovascular accident.
Main Results:
- BMC transplantation significantly improved LVEF in both revascularized (3.35%) and non-revascularized (3.05%) patient groups.
- In non-revascularized patients, BMCs significantly decreased LVESV (-11.75 ml) and LVEDV (-7.80 ml).
- Subgroup analysis indicated that transplantation route, baseline LVEF, and cell type influence BMC therapy efficacy.
Conclusions:
- Autologous BMC transplantation is safe and effective for CIHD patients, including those eligible for revascularization (CABG/PCI) and those not.
- Long-term follow-up and large-scale clinical trials are necessary to validate these findings and confirm sustained benefits.
Background:
Although bone marrow-derived cells (BMCs) have shown great therapeutic potential in patients with chronic ischemic heart disease (CIHD), the exact efficacy and safety of BMCs therapy is still not completely defined.
Material/Methods:
We searched PubMed, OVID, EMBASE, the Cochrane Library, and ClinicalTrials.gov and finally identified 20 qualified trials in this meta-analysis. Assessment of efficacy was based on left ventricular ejection fraction (LVEF), left ventricular end-systolic volume (LVESV), and left ventricular end-diastolic volume (LVEDV) improvement, by weighted mean difference (WMD) with 95% confidence intervals (CIs). RESULTS of all-cause death, ventricular arrhythmia, recurrent myocardial infarction, and cerebrovascular accident were pooled to assess safety. Subgroup analysis was performed by stratifying RCTs into 2 subgroups of those with revascularization and without revascularization.
Results:
BMC transplantation significantly improved LVEF in patients with revascularization (3.35%, 95% CI 0.72% to 5.97%, p=0.01; I2=85%) and without revascularization (3.05%, 95% CI 0.65% to 5.45%, p=0.01; I2=86%). In patients without revascularization, BMC transplantation was associated with significantly decreased LVESV (-11.75 ml, 95% CI -17.81 ml to -5.69 ml, p=0.0001; I2=81%), and LVEDV (-7.80 ml, 95% CI -15.31 ml to -0.29 ml, p=0.04; I2=39%). Subgroup analysis showed that the route of transplantation, baseline LVEF, and type of cells delivered could influence the efficacy of BMC transplantation.
Conclusions:
Autologous transplantation of BMCs was safe and effective for patients who were candidates for revascularization with CABG/PCI and those who were not. However, large clinical trials and long-term follow-up are required to confirm these benefits.
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