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Updated: May 7, 2026

Intramyocardial Cell Delivery: Observations in Murine Hearts
Published on: January 24, 2014
Intracoronary autologous mononucleated bone marrow cell infusion for acute myocardial infarction: results of the
Jérôme Roncalli1, Frédéric Mouquet, Christophe Piot
1Fédération de Cardiologie, CHU Toulouse, INSERM U858, Institut de Médecine Moléculaire de Rangueil, Université Paul Sabatier, Toulouse, France.
Autologous bone marrow cells (BMCs) improved myocardial viability in patients post-acute myocardial infarction (AMI) in multivariate analysis. Further trials are needed to confirm efficacy and identify patient subgroups benefiting from cardiac cell therapy.
Area of Science:
- Cardiology
- Regenerative Medicine
- Biomedical Engineering
Background:
- Intracoronary autologous bone marrow cells (BMCs) show modest cardiac function improvement post-acute myocardial infarction (AMI).
- The impact of BMC therapy on myocardial viability in patients with reduced left ventricular ejection fraction (LVEF) after AMI remains unclear.
- This study aimed to assess BMC therapy's effect on myocardial viability and identify predictors of improvement.
Purpose of the Study:
- To evaluate the efficacy of intracoronary autologous bone marrow cell (BMC) therapy in improving myocardial viability.
- To identify predictive factors for enhanced myocardial viability in patients following acute myocardial infarction (AMI).
- To assess the impact of BMC therapy on patients with decreased left ventricular ejection fraction (LVEF) post-AMI.
Main Methods:
- A randomized multicentre study involving 101 patients with AMI, successful reperfusion, LVEF ≤45%, and reduced myocardial viability.
- Patients were randomized into a control group (n=49) or a bone marrow cell (BMC) group (n=52).
- Myocardial viability was assessed 3 months post-AMI using resting Tl201-SPECT and radionuclide angiography.
Main Results:
- Myocardial viability improved in 34% of patients receiving BMCs versus 16% in the control group (P=0.06).
- Multivariate analysis revealed a significant improvement in myocardial viability in the BMC group compared to the control group (P=0.03).
- Active smoking (P=0.04) was associated with adverse outcomes, while microvascular obstruction showed a positive trend (P=0.07).
Conclusions:
- Intracoronary autologous BMC administration was associated with improved myocardial viability in multivariate analysis.
- Univariate analysis did not show a significant improvement, highlighting the need for further investigation.
- A large international trial is recommended to confirm cardiac cell therapy efficacy and define patient subgroups that benefit most.
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