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Clinical Benefits of Stem Cells for Chronic Symptomatic Systolic Heart Failure: A Systematic Review of the Existing Data and Ongoing Trials

机译:干细胞治疗慢性症状性收缩期心力衰竭的临床益处:现有数据的系统评价和正在进行的试验

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The benefits of stem cell therapy for patients with chronic symptomatic systolic heart failure due to ischemic and nonischemic cardiomyopathy (ICM and NICM, respectively) are unclear. We performed a systematic review of major published and ongoing trials of stem cell therapy for systolic heart failure and compared measured clinical outcomes for both types of cardiomyopathy. The majority of the 29 published studies demonstrated clinical benefits of autologous bone marrow-derived mesenchymal stem cells (BM-MSCs). Left ventricular ejection fraction (LVEF) was improved in the majority of trials after therapy. Cell delivery combined with coronary artery bypass grafting was associated with the greatest improvement in LVEF. Left ventricular end-systolic volume (or diameter), New York Heart Association functional classification, quality of life, and exercise capacity were also improved in most studies after cell therapy. Most ICM trials demonstrated a significant improvement in perfusion defects, infarct size, and myocardial viability. Several larger clinical trials that are in progress employ alternative delivery modes, cell types, and longer follow-up periods. Stem cells are a promising therapeutic modality for patients with heart failure due to ICM or NICM. More data are required from larger blinded trials to determine which combination of cell type and delivery mode will yield the most benefit with avoidance of harm in these patient populations.
机译:对于因缺血性和非缺血性心肌病(分别为ICM和NICM)导致的慢性症状性收缩期心力衰竭患者,干细胞疗法的益处尚不清楚。我们对干细胞疗法治疗收缩性心力衰竭的主要已发表和正在进行的试验进行了系统评价,并比较了两种类型的心肌病的临床测量结果。在发表的29项研究中,大多数证明了自体骨髓源间充质干细胞(BM-MSC)的临床益处。在治疗后的大多数试验中,左室射血分数(LVEF)均得到改善。细胞递送与冠状动脉搭桥术相结合可最大程度改善LVEF。细胞治疗后的大多数研究中,左心室收缩末期容积(或直径),纽约心脏协会的功能分类,生活质量和运动能力也得到了改善。大多数ICM试验表明,灌注缺陷,梗死面积和心肌生存能力都有显着改善。正在进行的几项较大的临床试验采用了其他的递送方式,细胞类型和更长的随访时间。对于因ICM或NICM而导致的心力衰竭患者,干细胞是一种有前途的治疗方式。需要从更大的盲试验中获得更多数据,以确定哪种细胞类型和递送方式组合将在避免这些患者群体受到伤害的情况下产生最大的益处。

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