Cocozza M, Picano T, Oliviero U, Russo N, Coto V, Milani M
IV Division of Internal Medicine, University of Naples, Italy.
Stroke. 1995 Apr;26(4):597-601. doi: 10.1161/01.str.26.4.597.
We assessed the effects of long-term treatment with picotamide, an antiplatelet agent with dual antithromboxane activity, on the evolution of early asymptomatic carotid atherosclerotic lesions in diabetic patients.
In a double-blind, placebo-controlled, 2-year study, 50 type II normotensive diabetic patients (35 men; mean age, 66 +/- 5 years) with asymptomatic mild or moderate nonstenotic (< 50%) carotid atherosclerotic lesions and negative history of cerebrovascular ischemic events were enrolled and randomly given picotamide (300 mg TID) or the corresponding placebo. A high-resolution, real-time B-scan echographic assessment of carotid arteries was performed at baseline and after 1, 3, 6, 12, 18, and 24 months of double-blind treatment. Prevalence and evolutionary trends of carotid atherosclerotic lesions (number per patient and mean stenosis expressed as percent) were considered as efficacy primary end points.
At baseline, mean +/- SD numbers of carotid atherosclerotic lesions per patient were 2.7 +/- 1.8 and 2.2 +/- 1.2 in the picotamide and placebo groups, respectively. Mean +/- SD percent stenosis was 25.3 +/- 7% in the picotamide group and 27.3 +/- 6% in the placebo group. Forty-nine patients completed the study. At month 24, the placebo group (n = 24) showed a significant progression in number of carotid atherosclerotic lesions (3.04 +/- 1.8; P < .02 versus baseline) and in mean percent stenosis (35 +/- 17%; 95% confidence interval, 33% to 37%; P < .01 versus baseline). In the picotamide group (n = 25), mean number of carotid atherosclerotic lesions (2.7 +/- 1.6) and percent stenosis (26 +/- 9%; 95% confidence interval, 24.8% to 27.2%) remained unchanged. At month 24, compared with randomized placebo, lesion numbers (P < .03) and percent stenosis (P < .01) in the picotamide group were significantly lower. During the study, 12 patients experienced major or minor ischemic vascular events (9 in the placebo group and 3 in the picotamide group; P = .07).
In diabetic patients compared with patients receiving placebo, long-term treatment with picotamide can slow the evolution of early carotid atherosclerotic lesions, inhibiting progression of plaque number and growth.
我们评估了吡考他胺(一种具有双重抗血栓素活性的抗血小板药物)长期治疗对糖尿病患者早期无症状性颈动脉粥样硬化病变进展的影响。
在一项双盲、安慰剂对照、为期2年的研究中,纳入了50例II型血压正常的糖尿病患者(35例男性;平均年龄66±5岁),这些患者有轻度或中度无症状性非狭窄(<50%)颈动脉粥样硬化病变且无脑血管缺血事件病史,并随机给予吡考他胺(300mg,每日三次)或相应的安慰剂。在基线以及双盲治疗1、3、6、12、18和24个月后,对颈动脉进行高分辨率实时B超扫描评估。颈动脉粥样硬化病变的患病率和演变趋势(每位患者的病变数量以及以百分比表示的平均狭窄程度)被视为主要疗效终点。
在基线时,吡考他胺组和安慰剂组每位患者颈动脉粥样硬化病变的平均±标准差数量分别为2.7±1.8和2.2±1.2。吡考他胺组的平均±标准差狭窄百分比为25.3±7%,安慰剂组为27.3±6%。49例患者完成了研究。在第24个月时,安慰剂组(n = 24)的颈动脉粥样硬化病变数量(3.04±1.8;与基线相比P <.02)和平均狭窄百分比(35±17%;95%置信区间,33%至37%;与基线相比P <.01)均有显著进展。在吡考他胺组(n = 25),颈动脉粥样硬化病变的平均数量(2.7±1.6)和狭窄百分比(26±9%;95%置信区间,24.8%至27.2%)保持不变。在第24个月时,与随机分组的安慰剂相比,吡考他胺组的病变数量(P <.03)和狭窄百分比(P <.01)显著更低。在研究期间,12例患者发生了主要或轻微的缺血性血管事件(安慰剂组9例,吡考他胺组3例;P =.07)。
与接受安慰剂的患者相比,糖尿病患者长期使用吡考他胺治疗可减缓早期颈动脉粥样硬化病变的进展,抑制斑块数量的增加和生长。