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Permanent Coronary Artery Occlusion: Cardiovascular MR Imaging Is Platform for Percutaneous Transendocardial Delivery and Assessment of Gene Therapy in Canine Model

机译:永久性冠状动脉阻塞:心血管MR成像是经皮心内膜递送和犬模型中基因治疗评估的平台

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摘要

>Purpose: To provide evidence that vascular endothelial growth factor (VEGF) genes delivered transendocardially with magnetic resonance (MR) imaging guidance may neovascularize or improve vascular recruitment in occlusive infarction.>Materials and Methods: All experimental procedures received approval from the institutional committee on animal research. Dogs with permanent coronary artery occlusion were imaged twice (3 days after occlusion for assessment of acute infarction; a mean of 50 days after occlusion ± 3 [standard error of the mean] for assessment of chronic infarction). A mixture of plasmid VEGF and plasmid LacZ (n = 6, treated animals) or plasmid LacZ and sprodiamide (n = 6, placebo control animals) was delivered to four sites. MR fluoroscopy was used to target and monitor delivery of genes. The effectiveness of this delivery approach was determined by using MR imaging methods to assess perfusion, left ventricular (LV) function, myocardial viability, and infarct resorption. Histologic evaluation of neovascularization was then performed.>Results: MR fluoroscopic guidance of injectates was successful in both groups. Treated animals with chronic, but not those with acute, infarction showed the following differences compared with control animals: (a) steeper mean maximum upslope perfusion (200 sec−1 ± 32 vs 117 sec−1 ± 15, P = .02), (b) higher peak signal intensity (1667 arbitrary units ± 100 vs 1132 arbitrary units ± 80, P = .002), (c) increased ejection fraction (from 27.9% ± 1.2 to 35.3% ± 1.6, P = .001), (d) smaller infarction size (as a percentage of LV mass) at MR imaging (8.5% ± 0.9 vs 11.3% ± 0.9, P = .048) and triphenyltetrazolium chloride staining (9.4% ± 1.5 vs 12.7% ± 0.4, P = .05), and (e) higher vascular density (as number of vessels per square millimeter) at the border (430 ± 117 vs 286 ± 19, P = .0001) and core (307 ± 112 vs 108 ± 17, P = .0001).>Conclusion: The validity of plasmid VEGF gene delivered with MR fluoroscopic guidance into occlusive infarction was confirmed by neovascularization associated with improved perfusion, LV function, and infarct resorption.© RSNA, 2008
机译:>目的:为提供证据,证明在磁共振(MR)成像指导下经心内膜递送的血管内皮生长因子(VEGF)基因可能使闭塞性梗塞新生血管化或改善血管募集。>材料和方法:所有实验程序均已获得动物研究机构委员会的批准。对具有永久性冠状动脉闭塞的狗进行两次成像(闭塞后3天用于评估急性梗塞;闭塞后50天的平均值±3 [平均值的标准误]用于评估慢性梗塞)。将质粒VEGF和质粒LacZ(n = 6,治疗的动物)或质粒LacZ和sprodiamide(n = 6,安慰剂对照动物)的混合物递送至四个位点。 MR透视用于靶向和监测基因的传递。通过使用MR成像方法评估灌注,左心室(LV)功能,心肌生存力和梗塞吸收来确定这种递送方法的有效性。然后进行了新血管形成的组织学评估。>结果:两组的MR透视检查均成功。与对照动物相比,患有慢性但未患有急性梗塞的治疗动物表现出以下差异:(a)平均最大上坡灌注值更陡(200 sec -1 ±32 vs 117 sec - 1 ±15,P = .02),(b)峰值信号强度更高(1667个任意单位±100对1132个任意单位±80,P = .002),(c)射血分数增加(从27.9%起) ±1.2至35.3%±1.6,P = .001),(d)MR成像(8.5%±0.9 vs 11.3%±0.9,P = .048)和氯化三苯基四唑鎓盐的梗死面积较小(占LV质量的百分比)染色(9.4%±1.5对12.7%±0.4,P = .05),(e)边界处的血管密度更高(每平方毫米的血管数)(430±117对286±19, P = .0001)和核心(307±112 vs 108±17, P = .0001)。>结论:质粒 VEGF < / em> MR荧光镜引导下传递至闭塞性梗死的基因已通过新血管形成与改善的血管闭塞性证实融合,左室功能和梗死吸收©RSNA,2008

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