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经皮逆行冠状窦输注自体骨髓单个核细胞移植治疗慢性难治性心绞痛的安全性和可行性。

Safety and feasibility of percutaneous retrograde coronary sinus delivery of autologous bone marrow mononuclear cell transplantation in patients with chronic refractory angina.

机构信息

Division of Interventional Cardiology and Regenerative Medicine, Clínica Maisón de Santé, Lima, Peru.

出版信息

J Transl Med. 2011 Oct 26;9:183. doi: 10.1186/1479-5876-9-183.

DOI:10.1186/1479-5876-9-183
PMID:22029669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3215661/
Abstract

BACKGROUND

Chronic refractory angina is a challenging clinical problem with limited treatment options. The results of early cardiovascular stem cell trials using ABMMC have been promising but have utilized intracoronary or intramyocardial delivery. The goal of the study was to evaluate the safety and early efficacy of autologous bone marrow derived mononuclear cells (ABMMC) delivered via percutaneous retrograde coronary sinus perfusion (PRCSP) to treat chronic refractory angina (CRA).

METHODS

From May 2005 to October 2006, 14 patients, age 68 +/- 20 years old, with CRA and ischemic stress-induced myocardial segments assessed by SPECT received a median 8.1910(8) ± 4.310(8) mononuclear and 1.6510(7) ± 1.4210(7) CD34(+) cells by PRCSP.

RESULTS

ABMMC delivery was successful in all patients with no arrhythmias, elevated cardiac enzymes or complications related to the delivery. All but one patient improved by at least one Canadian Cardiovascular Society class at 2 year follow-up compared to baseline (p < 0.001). The median baseline area of ischemic myocardium by SPECT of 38.2% was reduced to 26.5% at one year and 23.5% at two years (p = 0.001). The median rest left ventricular ejection fraction by SPECT at baseline was 31.2% and improved to 35.5% at 2 year follow up (p = 0.019).

CONCLUSIONS

PRCSP should be considered as an alternative method of delivery for cell therapy with the ability to safely deliver large number of cells regardless of coronary anatomy, valvular disease or myocardial dysfunction. The clinical improvement in angina, myocardial perfusion and function in this phase 1 study is encouraging and needs to be confirmed in randomized placebo controlled trials.

摘要

背景

慢性难治性心绞痛是一种具有挑战性的临床问题,治疗选择有限。使用 ABMMC 的早期心血管干细胞试验结果令人鼓舞,但均采用了冠状动脉内或心肌内给药。本研究的目的是评估通过经皮逆行冠状窦灌注(PRCSP)递送自体骨髓来源的单核细胞(ABMMC)治疗慢性难治性心绞痛(CRA)的安全性和早期疗效。

方法

2005 年 5 月至 2006 年 10 月,14 名年龄 68 ± 20 岁的 CRA 患者和 SPECT 评估的缺血性应激诱导心肌节段接受中位数 8.1910(8) ± 4.310(8)个单核细胞和 1.6510(7) ± 1.4210(7)个 CD34(+)细胞的 PRCSP。

结果

所有患者的 ABMMC 递送均成功,无心律失常、心肌酶升高或与递送相关的并发症。与基线相比,2 年随访时除 1 例患者外,所有患者至少提高了一个加拿大心血管学会(CCS)心绞痛分级(p < 0.001)。SPECT 测量的基线缺血心肌面积中位数从 38.2%减少到 1 年时的 26.5%和 2 年时的 23.5%(p = 0.001)。SPECT 测量的基线静息左心室射血分数中位数为 31.2%,2 年随访时改善至 35.5%(p = 0.019)。

结论

PRCSP 应被视为细胞治疗的另一种给药方法,无论冠状动脉解剖、瓣膜疾病或心肌功能障碍如何,均可安全地输送大量细胞。这项 1 期研究中心绞痛、心肌灌注和功能的临床改善令人鼓舞,需要在随机安慰剂对照试验中得到证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/4287b93f9376/1479-5876-9-183-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/997ae0964bad/1479-5876-9-183-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/d0e90c1a2f89/1479-5876-9-183-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/4f9659f02ff8/1479-5876-9-183-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/eec3f24116fc/1479-5876-9-183-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/4287b93f9376/1479-5876-9-183-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/997ae0964bad/1479-5876-9-183-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/d0e90c1a2f89/1479-5876-9-183-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/4f9659f02ff8/1479-5876-9-183-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/eec3f24116fc/1479-5876-9-183-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/3215661/4287b93f9376/1479-5876-9-183-5.jpg

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