Key result
Implantation of bone marrow cells from old donor mice failed to prevent the decline in left ventricular ejection fraction post-myocardial infarction, unlike cells from young donors which significantly improved cardiac function.
Why the study?
Does advanced donor age impair the therapeutic efficacy of bone marrow cells in improving left ventricular function post-myocardial infarction?
Does advanced donor age impair the therapeutic efficacy of bone marrow cells in improving left ventricular function post-myocardial infarction?
Absolute Event Rate: 23.8% vs 39%
p-value: p=<0.001
Advanced donor age and concurrent donor MI additively impair the therapeutic efficacy of bone marrow cells for post-MI cardiac repair, potentially explaining the modest results of clinical autologous cell therapy trials.
May caution against autologous bone marrow cell therapy from elderly donors post-MI; leaves open whether young or rejuvenated cells improve outcomes in clinical trials.
Therapeutic results of clinical autologous bone marrow cell (BMC) therapy trials for cardiac disease have been modest compared to results of BMC implantation into rodent hearts post-myocardial infarction (MI). In clinical trials, autologous BMCs are typically harvested from older patients who have recently suffered an MI. In contrast, experimental studies in rodent models typically utilize donor BMCs isolated from young, healthy, inbred mice that are not the recipients. Using unfractionated BMCs from donor mice at ages of young, middle-aged, and old, we discovered that recipient left ventricular function post-MI was significantly improved by young donor BMC implantation but was only preserved by middle-aged donor BMCs. Notably, old donor BMCs did not slow the decline in recipient post-MI cardiac function, suggesting BMC impairment by advanced donor age. Furthermore, we also show here that BMCs that are therapeutically impaired by donor age can be further impaired by concurrent donor MI. In conclusion, our findings suggest that therapeutic impairment of BMCs by advanced age is one of the important factors that can limit the success of clinical autologous BMC-based therapy.
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Xiaoyin Wang (2011) studied Myocardial infarction (n=58). Bone marrow cells from old donors vs. Bone marrow cells from young donors or HBSS vehicle was evaluated on Left ventricular ejection fraction (EF) at 28 days post-MI (p=<0.001). Implantation of bone marrow cells from old donor mice failed to prevent the decline in left ventricular ejection fraction post-myocardial infarction, unlike cells from young donors which significantly improved cardiac function.
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