Department of Vascular and Endovascular Surgery, Second Affiliated Hospital of Naval Medical University, District of Huangpu, Fengyang Road 415, Shanghai 200003, China.
Department of Vascular and Endovascular Surgery, Second Affiliated Hospital of Naval Medical University, District of Huangpu, Fengyang Road 415, Shanghai 200003, China.
Phytomedicine. 2022 Nov;106:154408. doi: 10.1016/j.phymed.2022.154408. Epub 2022 Aug 19.
Aspirin is an effective antiplatelet agent for the treatment of carotid atherosclerosis. However, the high risk of bleeding events associated with the drug makes it necessary to seek a safer alternative, with similar or more efficacy than aspirin. Dengzhan Shengmai (DZSM) capsules have been widely used to treat carotid atherosclerosis, and if proven to be non-inferior to aspirin, it may be preferable over the latter for carotid atherosclerosis treatment due to its numerous advantages. We conducted a randomised trial to test the non-inferiority of DZSM to aspirin for the treatment of carotid atherosclerotic plaques.
We performed a single-centre, prospective, open-label, randomised non-inferiority trial. Patients with carotid atherosclerotic plaques were enrolled and randomly assigned (1:1) to receive either DZSM capsules or aspirin. The follow-up period was 12 months. The primary outcome was the mean change in carotid intima-media thickness (IMT). Secondary outcomes included ischaemic events, rate of lumen stenosis, lipid levels, and plaque scores, length, counts, and vulnerability. Adverse events and laboratory test results were recorded as safety outcomes. The non-inferiority of DZSM was demonstrated when the lower limit of the one-sided 97.5% confidence interval (CI) of the difference in IMT between groups was more than -0.06 mm (margin of non-inferiority). This trial has been registered at ClinicalTrials.gov (CHiCTR1900021365).
From 1 April 2019 to 30 September 2019, 150 patients were enrolled, and there was no statistical difference in demographics between the groups. Intention-to-treat analysis showed that the decrease in IMT(IMT) was 0.216 ± 0.160 and 0.225 ± 0.149 mm in the DZSM and aspirin groups, respectively. The one-sided 97.5% CI for the difference between IMTs was (-0.0593, +∞). The non-inferiority of DZSM was demonstrated (P = 0.0234). There was no significant difference in the incidence of ischaemic events between the groups (P = 1.0). The DZSM group had significantly reduced plaque scores (P < 0.0001), length (P < 0.0001), and counts (P < 0.0001), and improved plaque vulnerability (P < 0.0001). The DZSM group also had reduced levels of low-density lipoprotein cholesterol (LDL-C) (P < 0.0001). Finally, the DZSM group had a lower incidence of total adverse events (14.7% vs. 28%, P = 0.046), especially gastrointestinal discomfort (5.3% vs. 16%, P = 0.034). Although there was no significant difference in bleeding events (0 vs. 5.3%, P = 0.120), the DZSM group tended to have a lower incidence.
This trial demonstrated that DZSM was not inferior, in efficacy, to aspirin in treating carotid atherosclerotic plaques, and was found to be superior to aspirin in terms of safety. This study provides a new approach for treating carotid plaques, especially in aspirin-intolerant patients.
阿司匹林是治疗颈动脉粥样硬化的有效抗血小板药物。然而,由于该药物出血风险较高,因此需要寻找一种更安全的替代药物,其疗效与阿司匹林相当或更优。灯盏生脉胶囊(DZSM)已广泛用于治疗颈动脉粥样硬化,如果证明其与阿司匹林相比不劣于后者,由于其诸多优点,可能更适合用于颈动脉粥样硬化的治疗。我们进行了一项随机试验,以测试 DZSM 与阿司匹林治疗颈动脉粥样硬化斑块的非劣效性。
我们进行了一项单中心、前瞻性、开放标签、随机非劣效性试验。纳入颈动脉粥样硬化斑块患者,并随机(1:1)分配至接受 DZSM 胶囊或阿司匹林治疗。随访时间为 12 个月。主要结局为颈动脉内-中膜厚度(IMT)的平均变化。次要结局包括缺血性事件、管腔狭窄率、血脂水平以及斑块评分、长度、数量和易损性。记录不良反应和实验室检查结果作为安全性结局。当组间 IMT 差异的单侧 97.5%置信区间(CI)下限大于-0.06mm(非劣效性边界)时,证明 DZSM 具有非劣效性。该试验已在 ClinicalTrials.gov(CHiCTR1900021365)注册。
2019 年 4 月 1 日至 2019 年 9 月 30 日,共纳入 150 例患者,两组间的人口统计学特征无统计学差异。意向治疗分析显示,DZSM 组和阿司匹林组的 IMT 下降分别为 0.216±0.160mm 和 0.225±0.149mm。IMT 差值的单侧 97.5%CI 为(-0.0593,+∞)。证明 DZSM 具有非劣效性(P=0.0234)。两组间缺血性事件的发生率无统计学差异(P=1.0)。DZSM 组斑块评分(P<0.0001)、长度(P<0.0001)和数量(P<0.0001)显著降低,斑块易损性(P<0.0001)改善。DZSM 组还降低了低密度脂蛋白胆固醇(LDL-C)水平(P<0.0001)。最后,DZSM 组总不良反应发生率(14.7%比 28%,P=0.046)较低,特别是胃肠道不适(5.3%比 16%,P=0.034)发生率较低。尽管两组出血事件(0 比 5.3%,P=0.120)发生率无统计学差异,但 DZSM 组出血事件发生率较低。
本试验表明,DZSM 在治疗颈动脉粥样硬化斑块方面与阿司匹林相当,且在安全性方面优于阿司匹林。本研究为治疗颈动脉斑块提供了一种新方法,特别是在阿司匹林不耐受的患者中。