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Cell treatment after acute myocardial infarction prevents early decline in circulating IGF-1
Haakon K Grøgaard1, Ingebjørg Seljeflot, Ketil Lunde
1Institute for Experimental Medical Research, Oslo University Hospital, Ullevål, University of Oslo, Oslo, Norway. h.k.grogaard@medisin.uio.no
Insights
Bone marrow cell therapy after myocardial infarction impacts insulin-like growth factor-1 (IGF-1) levels. Higher IGF-1 concentrations were associated with improved left ventricular ejection fraction in patients.
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Molecular Cardiology
Background:
- Acute myocardial infarction (AMI) can lead to impaired left ventricular (LV) function.
- Intracoronary cell transplantation is being investigated as a therapeutic strategy post-AMI.
- The impact of cell therapy on circulating growth factors and LV function requires elucidation.
Purpose of the Study:
- To investigate the effect of intracoronary autologous bone marrow cell transplantation on circulating growth factors after AMI.
- To determine the relationship between changes in growth factors and left ventricular function.
Main Methods:
- The ASTAMI study randomized patients to receive either cell treatment or a control.
- Circulating levels of insulin-like growth factor-1 (IGF-1), hepatocyte growth factor (HGF), stromal derived factor-1-alpha (SDF-1α), and transforming growth factor beta (TGF-β) were measured.
- Left ventricular ejection fraction (LVEF) was assessed using single photon emission computed tomography at six months.
Main Results:
- A significant difference in IGF-1 change from baseline to three months was observed between the cell treatment and control groups (p = 0.024).
- A weak but significant correlation (r = 0.24, p = 0.02) was found between LVEF and averaged IGF-1 concentrations.
- Patients with IGF-1 levels above the median demonstrated a significantly higher LVEF (52.3%) compared to those below the median (46.4%, p = 0.017).
Conclusions:
- Intracoronary bone marrow cell treatment following myocardial infarction appears to attenuate the reduction in circulating IGF-1.
- IGF-1 levels over time showed a weak but significant correlation with left ventricular ejection fraction.
Objectives:
To examine the influence of intracoronary autologous bone marrow cell transplantation after acute myocardial infarction on circulating growth factors and their relationship to left ventricular function.
Methods:
Circulating insulin-like growth factor-1 (IGF-1), hepatocyte growth factor (HGF), stromal derived factor-1-alpha (SDF-1α), and transforming growth factor beta (TGF-β) were measured in patients randomized to cell treatment or control, in the ASTAMI study. Autologous cells were injected intracoronary on day 6; blood was sampled on days 5, 9, and at three months. Left ventricular ejection fraction was recorded by electrocardiogram-gated single photon emission computed tomography at six months.
Results:
Only change in IGF-1 from baseline to three months differed between groups (p = 0.024). A weak but significant correlation was found between left ventricular ejection fraction and the averaged IGF-1 concentrations of all patients (r = 0.24, p = 0.02). Patients with IGF-1 above or below median (102 ng/ml) had a left ventricular ejection fraction of 52.3% (±11.4) versus 46.4% (±12.2) respectively (p = 0.017).
Conclusions:
Intracoronary bone marrow cell treatment after myocardial infarction attenuates a reduction in circulating IGF-1. IGF-1 levels over time were weakly, but significantly correlated to left ventricular ejection fraction.
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