Oguz E, Ayik F, Ozturk P, Engin C, Nalbantgil S, Yagdi T, Ozbaran M
Department of Cardiovascular Surgery, Ege University Medical Faculty, Izmir, Turkey.
Transplant Proc. 2011 Apr;43(3):931-4. doi: 10.1016/j.transproceed.2011.01.115.
The aim of this study was to assess the long-term efficacy of stem cell transplantation with revascularization for patients with ischemic cardiomyopathy.
We enrolled 17 patients with ischemic cardiomyopathy who had undergone autologous stem cell treatment. To assess myocardial ischemia and viability they underwent coronary angiography, stress tests with dobutamine, echocardiography, and positron emission tomography. Peripheral stem cells mobilized using granulocyte colony-stimulating factor (G-CSF) were collected by aphseresis for transplantation transmyocardially into the areas of injury during coronary artery bypass surgery to increase blood flow to the engrafted areas.
Three patients died in the early follow-up period and 4 patients with cardiac failure died during mid-term follow-up; they all underwent stem cell transplantation at 6 months after acute myocardial infarction. The mean follow-up period of the remaining 10 patients was 85.8 ± 9.2 months (range, 70-100). Mean left ventricular ejection fraction improved to 30.0 ± 6.7, whereas the preoperative mean left ventricular ejection fraction of the surviving patients was 25.6 ± 4.5 (P = .035). Mean New York Heart Association (NYHA) functional class decreased from 3.2 to 1.5 (P = .006). When the study population was divided into 2 subgroups according to the interval between acute myocardial infraction and surgery, the patients who underwent autologous stem cell transplantation within the first 6 months after myocardial infraction (Group 1) showed significantly lower NYHA scores at the last follow-up (P = .024 in Group 1 and P = .102 in Group 2). No side effects were observed to be due to the stem cell or G-CSF injections.
Treatment of ischemic cardiomyopathy with autologous stem cell transplantation is easy and safe, opening a new window in the treatment of "no hope" patients.
本研究旨在评估血管再生的干细胞移植对缺血性心肌病患者的长期疗效。
我们纳入了17例接受过自体干细胞治疗的缺血性心肌病患者。为评估心肌缺血和存活情况,他们接受了冠状动脉造影、多巴酚丁胺负荷试验、超声心动图和正电子发射断层扫描。使用粒细胞集落刺激因子(G-CSF)动员的外周干细胞通过单采术收集,以便在冠状动脉搭桥手术期间经心肌移植到损伤区域,以增加移植区域的血流量。
3例患者在早期随访期死亡,4例心力衰竭患者在中期随访期死亡;他们均在急性心肌梗死后6个月接受了干细胞移植。其余10例患者的平均随访期为85.8±9.2个月(范围70 - 100个月)。平均左心室射血分数提高到30.0±6.7,而存活患者术前的平均左心室射血分数为25.6±4.5(P = 0.035)。纽约心脏协会(NYHA)功能分级平均从3.2降至1.5(P = 0.006)。根据急性心肌梗死与手术之间的间隔将研究人群分为2个亚组时,在心肌梗死后前6个月内接受自体干细胞移植的患者(第1组)在最后一次随访时NYHA评分显著更低(第1组P = 0.024,第2组P = 0.102)。未观察到由干细胞或G-CSF注射引起的副作用。
自体干细胞移植治疗缺血性心肌病简便安全,为“无希望”患者的治疗打开了一扇新窗口。