Department of Cardiothoracic and Vascular Surgery, Deutsches Herzzentrum Berlin, Augustenburger Platz 1, Berlin 13353, Germany.
Pediatric Bone Marrow Transplant Program, Charité, Universitätsmedizin Berlin, Berlin 10117, Germany.
Eur Heart J. 2014 May 14;35(19):1263-74. doi: 10.1093/eurheartj/ehu007. Epub 2014 Feb 3.
AIMS: Intra-myocardial transplantation of CD133(+) bone marrow stem cells (BMC) yielded promising results in clinical pilot trials. We now performed the double-blinded, randomized, placebo-controlled CARDIO133 trial to determine its impact on left ventricular (LV) function and clinical symptoms. METHODS AND RESULTS: Sixty patients with chronic ischaemic heart disease and impaired LV function (left ventricular ejection fraction, LVEF <35%) were randomized to undergo either coronary artery bypass grafting (CABG) and injection of CD133(+) BMC in the non-transmural, hypokinetic infarct border zone (CD133), or CABG and placebo injection (placebo). Pre-operative LVEF was 27 ± 6% in CD133 patients and 26 ± 6% in placebo patients. Outcome was assessed after 6 months, and the primary endpoint was LVEF measured by cardiac magnetic resonance imaging (MRI) at rest. The incidence of adverse events was similar in both groups. There was no difference in 6-min walking distance, Minnesota Living with Heart Failure score, or Canadian Cardiovascular Society (CCS) class between groups at follow-up, and New York Heart Association class improved more in the placebo group (P = 0.004). By cardiac MRI, LVEF at 6 months was 33 ± 8% in the placebo group and 31 ± 7% in verum patients (P = 0.3), with an average inter-group difference of -2.1% (95% CI -6.3 to 2.1). Systolic or diastolic LV dimensions at 6 months were not different, either. In the CD133 group, myocardial perfusion at rest recovered in more LV segments than in the placebo group (9 vs. 2%, P < 0.001). Scar mass decreased by 2.2 ± 5 g in CD133(+) patients (P = 0.05), but was unchanged in the placebo group (0.3 ± 4 g, P = 0.7; inter-group difference in change = 2 g (95% CI -1.1 to 5)). By speckle-tracking echocardiography, cell-treated patients showed a better recovery of regional wall motion when the target area was posterior. CONCLUSION: Although there may be some improvements in scar size and regional perfusion, intra-myocardial injection of CD133(+) BMC has no effect on global LV function and clinical symptoms. Improvements in regional myocardial function are only detectable in patients with posterior infarction, probably because the interventricular septum after anterior infarction is not accessible by trans-epicardial injection. CLINICAL TRIAL REGISTRATION: This trial was registered at http://www.clinicaltrials.gov under NCT00462774.
目的:将 CD133(+)骨髓干细胞(BMC)进行心肌内移植在临床初步试验中取得了良好的效果。我们现在进行了双盲、随机、安慰剂对照的 CARDIO133 试验,以确定其对左心室(LV)功能和临床症状的影响。
方法和结果:60 名患有慢性缺血性心脏病和 LV 功能受损(左心室射血分数,LVEF<35%)的患者被随机分为两组:冠状动脉旁路移植术(CABG)和在非透壁、运动不良的梗死边界区注射 CD133(+)BMC(CD133 组),或 CABG 和安慰剂注射(安慰剂组)。CD133 组患者术前 LVEF 为 27±6%,安慰剂组为 26±6%。术后 6 个月评估结果,主要终点为心脏磁共振成像(MRI)在静息状态下测量的 LVEF。两组患者的不良事件发生率相似。随访时,两组 6 分钟步行距离、明尼苏达州心力衰竭生活质量评分或加拿大心血管学会(CCS)分级无差异,安慰剂组纽约心脏协会(NYHA)心功能分级改善更明显(P=0.004)。心脏 MRI 显示,安慰剂组 6 个月时 LVEF 为 33±8%,而真药组为 31±7%(P=0.3),两组间平均差异为-2.1%(95%CI-6.3 至 2.1)。6 个月时的左心室收缩或舒张内径也无差异。在 CD133 组,与安慰剂组相比,更多的 LV 节段在静息状态下的心肌灌注得到恢复(9 个 vs. 2%,P<0.001)。CD133(+)患者的疤痕质量减少了 2.2±5g(P=0.05),但安慰剂组无变化(0.3±4g,P=0.7;组间变化差异为 2g(95%CI-1.1 至 5))。通过斑点追踪超声心动图,当目标区域为后部时,接受细胞治疗的患者的局部壁运动恢复更好。
结论:尽管 CD133(+)骨髓干细胞心肌内注射可能会导致疤痕大小和局部灌注的改善,但对整体 LV 功能和临床症状没有影响。仅在后壁梗死的患者中才能检测到局部心肌功能的改善,这可能是因为前壁梗死的室间隔无法通过心外膜注射到达。
临床试验注册:该试验在 http://www.clinicaltrials.gov 上注册,编号为 NCT00462774。
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