Zhang Qi, Lu Lin, Pu LiJin, Zhang RuiYan, Shen Jie, Zhu ZhengBing, Hu Jian, Yang ZhenKun, Chen QiuJin, Shen WeiFeng
Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, PR China.
Cardiovasc Diabetol. 2007 Jun 5;6:16. doi: 10.1186/1475-2840-6-16.
Observational clinical studies have shown that patients with diabetes have less favorable results after percutaneous coronary intervention compared with the non-diabetic counterparts, but its mechanism remains unclear. The aim of this study was to examine the changes of neointimal hyperplasia after sirolimus-eluting stent (SES) implantation in a diabetic porcine model, and to evaluate the impact of aortic inflammation on this proliferative process.
Diabetic porcine model was created with an intravenous administration of a single dose of streptozotocin in 15 Chinese Guizhou minipigs (diabetic group); each of them received 2 SES (Firebird, Microport Co, China) implanted into 2 separated major epicardial coronary arteries. Fifteen non-diabetic minipigs with SES implantation served as controls (control group). At 6 months, the degree of neointimal hyperplasia was determined by repeat coronary angiography, intravascular ultrasound (IVUS) and histological examination. Tumor necrosis factor (TNF)-alpha protein level in the aortic intima was evaluated by Western blotting, and TNF-alpha, interleukin (IL)-1beta and IL-6 mRNA levels were assayed by reverse transcription and polymerase chain reaction.
The distribution of stented vessels, diameter of reference vessels, and post-procedural minimal lumen diameter were comparable between the two groups. At 6-month follow-up, the degree of in-stent restenosis (40.4 +/- 24.0% vs. 20.2 +/- 17.7%, p < 0.05), late lumen loss (0.33 +/- 0.19 mm vs. 0.10 +/- 0.09 mm, p < 0.001) by quantitative angiography, percentage of intimal hyperplasia in the stented area (26.7 +/- 19.2% vs. 7.3 +/- 6.1%, p < 0.001) by IVUS, and neointimal area (1.59 +/- 0.76 mm2 vs. 0.41 +/- 0.18 mm2, p < 0.05) by histological examination were significantly exacerbated in the diabetic group than those in the controls. Significant increases in TNF-alpha protein and TNF-alpha, IL-1beta and IL-6 mRNA levels were observed in aortic intima in the diabetic group.
Neointimal hyperplasia persisted at least up to 6 months after SES implantation in diabetic porcine, which may be partly related to an exaggerated inflammatory response within the blood vessel wall. Our results provide theoretical support for potential direct beneficial effects of anti-diabetic and anti-inflammation medications in reducing the risk of restenosis after stenting.
观察性临床研究表明,与非糖尿病患者相比,糖尿病患者经皮冠状动脉介入治疗后的效果较差,但其机制尚不清楚。本研究的目的是在糖尿病猪模型中研究西罗莫司洗脱支架(SES)植入后新生内膜增生的变化,并评估主动脉炎症对这一增殖过程的影响。
对15只中国贵州小型猪静脉注射单剂量链脲佐菌素建立糖尿病猪模型(糖尿病组);每只猪在两条不同的主要心外膜冠状动脉中植入2枚SES(Firebird,微创医疗器械(上海)有限公司)。15只植入SES的非糖尿病小型猪作为对照组(对照组)。6个月时,通过重复冠状动脉造影、血管内超声(IVUS)和组织学检查确定新生内膜增生程度。通过蛋白质印迹法评估主动脉内膜中肿瘤坏死因子(TNF)-α蛋白水平,通过逆转录和聚合酶链反应检测TNF-α、白细胞介素(IL)-1β和IL-6 mRNA水平。
两组之间支架血管的分布、参考血管直径和术后最小管腔直径相当。在6个月的随访中,糖尿病组的支架内再狭窄程度(40.4±24.0%对20.2±17.7%,p<0.05)、定量血管造影显示的晚期管腔丢失(0.33±0.19 mm对0.10±0.09 mm,p<0.001)、IVUS显示的支架区域内膜增生百分比(26.7±19.2%对7.3±6.1%,p<0.001)以及组织学检查显示的新生内膜面积(1.59±0.76 mm2对0.41±0.