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Bone marrow-derived mononuclear cell therapy for nonischaemic dilated cardiomyopathy-A meta-analysis
Yanting Wen1, Jingjing Ding2, Bin Zhang1
1Center of Translational Medicine, Jiangsu Key Laboratory of Molecular Medicine, Nanjing University Medical School, Nanjing, China.
Insights
Bone marrow-derived mononuclear cells (BMMNCs) transplantation moderately improves left ventricular ejection fraction (LVEF) in non-ischaemic dilated cardiomyopathy (DCM) patients. Further research with larger populations and longer follow-up is recommended.
Area of Science:
- Cardiology
- Regenerative Medicine
- Cell Therapy
Background:
- Non-ischaemic dilated cardiomyopathy (DCM) poses a significant therapeutic challenge.
- The efficacy of bone marrow-derived mononuclear cells (BMMNCs) transplantation in DCM remains debated due to conflicting trial results.
Purpose of the Study:
- To systematically evaluate the impact of BMMNCs transplantation on left ventricular ejection fraction (LVEF) in patients with non-ischaemic DCM.
- To synthesize evidence from randomized controlled trials (RCTs) to clarify treatment effects.
Main Methods:
- A meta-analysis was conducted using data from seven RCTs involving 463 patients.
- Searches were performed across PubMed, EMBASE, and the Cochrane Controlled Trials Register for relevant studies.
Main Results:
- BMMNCs transplantation significantly improved LVEF by 3.79% (P = .007) and reduced LVESV by -24.36 mL (P = .03).
- No significant impact on all-cause mortality was observed (OR 0.92; P = .84).
- Improved LVEF was more pronounced with longer follow-up periods and when using pure BMMNCs compared to G-CSF-stimulated cells.
Conclusions:
- BMMNCs transplantation offers a moderate but statistically significant improvement in LVEF for non-ischaemic DCM.
- The findings support the need for larger RCTs with extended follow-up to further validate BMMNCs therapy.
Objective:
The therapeutic effects of bone marrow-derived mononuclear cells (BMMNCs) transplantation in patients with nonischaemic dilated cardiomyopathy (DCM) are still under debate. Current randomized controlled trials (RCTs) reported conflicting results. The aim of this study was to assess the effects of BMMNCs transplantation on left ventricular ejection fraction (LVEF) in patients with nonischaemic DCM.
Methods:
A comprehensive search of PubMed, EMBASE and Cochrane Controlled Trials Register was performed. We included RCTs reporting data on LVEF in patients with nonischaemic DCM after BMMNCs transplantation.
Results:
Seven RCTs including 463 patients were included. BMMNCs transplantation significantly improved LVEF by 3.79% (95% CI: 0.56%-7.03%; P = .007) and LVESV by -24.36 mL (95% CI: -46.36 to -2.36 mL; P = .03), while had no impact on the risk of all-cause death (OR 0.92; 95% CI: 0.41 to 2.08%; P = .84). Subgroup analysis demonstrated a more significant improvement of LVEF in patients with longer follow-up (~15 months to 5 years) than shorter ones (12 months). Moreover, using bone marrow mononuclear cells was more effective than using G-CSF-stimulated bone marrow/peripheral blood stem cells in the improvement of LVEF in patients with nonischaemic DCM.
Conclusions:
Bone marrow-derived mononuclear cells transplantation is associated with a moderate, but significant, improvement in LVEF in patients with nonischaemic DCM. This meta-analysis supports further RCT conductions using BMMNCs transplantation with larger patient's population and longer term follow-up.
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