Takagi Tsutomu, Yamamuro Atsushi, Tamita Koichi, Yamabe Kenji, Katayama Minako, Mizoguchi Shin, Ibuki Motoaki, Tani Tomoko, Tanabe Kazuaki, Nagai Kunihiko, Shiratori Kenichi, Morioka Shigefumi, Yoshikawa Junichi
Takagi Cardiology Clinic, Kyoto, Japan.
Am Heart J. 2003 Aug;146(2):E5. doi: 10.1016/S0002-8703(03)00146-7.
It has been reported that pioglitazone reduces neointimal hyperplasia after balloon-induced vascular injury in an experimental model.
To determine whether pioglitazone reduces neointimal tissue proliferation after coronary stent implantation in patients with type 2 diabetes mellitus, we studied 44 stented lesions in 44 patients with diabetes mellitus who underwent successful coronary stent implantation. Study patients were randomized into 2 groups: the pioglitazone group (23 patients with 23 lesions) and the control group (21 patients with 21 lesions). All patients underwent serial quantitative coronary angiography and serial intravascular ultrasound scanning studies. With a motorized pullback system, multiple image slices within the stent were obtained at every 1 mm. The stent area and lumen area were measured, and the neointimal area was calculated. Measurements were averaged over the number of selected image slices. The neointimal index was calculated as the averaged neointimal area divided by the averaged stent area multiplied by 100 (%).
After 6 months of treatment, angiographic in-stent restenosis (17% vs 43%, respectively, P =.0994) and target lesion revascularization (13% vs 38%, respectively, P =.0835) were less frequent in the pioglitazone group than the control group; however, these differences did not reach significance. The intravascular ultrasound scanning study demonstrated that the neointimal index in the pioglitazone group was significantly smaller than that in the control group (28% +/- 9% vs 48% +/- 15%, respectively, P <.0001).
A serial intravascular ultrasound scanning assessment demonstrated that pioglitazone reduces neointimal tissue proliferation after coronary stent implantation in patients with type 2 diabetes mellitus.
据报道,在实验模型中,吡格列酮可减少球囊诱导的血管损伤后的内膜增生。
为确定吡格列酮是否能减少2型糖尿病患者冠状动脉支架植入术后的内膜组织增殖,我们研究了44例成功接受冠状动脉支架植入术的糖尿病患者的44个支架植入病变。研究患者被随机分为两组:吡格列酮组(23例患者,23个病变)和对照组(21例患者,21个病变)。所有患者均接受了系列定量冠状动脉造影和系列血管内超声扫描研究。使用电动回撤系统,每隔1毫米获取支架内的多个图像切片。测量支架面积和管腔面积,并计算内膜面积。测量值在选定图像切片数量上进行平均。内膜指数计算为平均内膜面积除以平均支架面积再乘以100(%)。
治疗6个月后,吡格列酮组的血管造影支架内再狭窄(分别为17%对43%,P = 0.0994)和靶病变血管重建(分别为13%对38%,P = 0.0835)的发生率低于对照组;然而,这些差异未达到显著水平。血管内超声扫描研究表明,吡格列酮组的内膜指数显著小于对照组(分别为28%±9%对48%±15%,P < 0.0001)。
系列血管内超声扫描评估表明,吡格列酮可减少2型糖尿病患者冠状动脉支架植入术后的内膜组织增殖。