Brie Daniel Miron, Mornos Cristian, Brie Diduta Alina, Luca Constantin Tudor, Petrescu Lucian, Boruga Madalina
Department of Interventional Cardiology, Cardiovascular Disease Institute Timisoara, 300310 Timisoara, Romania.
Department of Cardiology, Department of Toxicology and Drug Industry, 'Victor Babes' University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Exp Ther Med. 2022 Jun;23(6):378. doi: 10.3892/etm.2022.11305. Epub 2022 Apr 8.
The link between inflammation and acute coronary syndrome (ACS) remains to be sufficiently elucidated. It has been previously suggested that there is an inflammatory process associated with ACS. Pentoxifylline, a methylxanthine derivate, is known to delay the progression of atherosclerosis and reduce the risk of vascular events, especially by modulating the systemic inflammatory response. The present study is a single-blind, randomized, prospective study of pentoxifylline 400 mg three times a day (TID) added to standard therapy vs. standard therapy plus placebo in ACS patients with non-ST elevation myocardial infarction (NSTEMI). Patients with ACS were randomized to receive standard therapy plus placebo in one arm (group A; aspirin, clopidogrel or ticagrelor, statin) and in the other arm (group B) pentoxifylline 400 mg TID was added to standard therapy. The primary outcome was the rate of major adverse cardiovascular events (MACEs) at 1 year. A total of 500 patients underwent randomization (with 250 assigned to group A and 250 to group B) and were followed-up for a median of 20 months. The mean age of the patients was 62.3±10.3 years, 80.4% were male, 20.8% had diabetes, 49.4% had hypertension, and 42% were currently smoking. The statistical analysis was performed for 209 patients in group A and 210 patients in group B (after dropouts due to study drug discontinuation). A primary endpoint occurred in 12.38% (n=26) of patients in group B, as compared with 15.78% (n=33) of those in group A [relative risk (RR), 0.78; 95% confidence interval (CI), 0.486-0.1.263; P=0.40], including cardiovascular death (RR, 0.93; 95% CI, 0.48-1.80, P=0.84), non-fatal myocardial infarction (RR, 1.1; 95% CI, 0.39-3.39, P=0.78), stroke (RR, 0.99; 95% CI, 0.14-6.99, P=0.99) and coronary revascularization (RR, 0.12; 95% CI, 0.015-0.985, P=0.048). Thus, adding pentoxifylline to standard treatment in patients with ACS did not improve MACE at 1 year but had some benefit on the need for coronary revascularization.
炎症与急性冠状动脉综合征(ACS)之间的联系仍有待充分阐明。此前已有研究表明,ACS存在一个炎症过程。己酮可可碱是一种甲基黄嘌呤衍生物,已知其可延缓动脉粥样硬化进展,降低血管事件风险,尤其是通过调节全身炎症反应来实现。本研究是一项单盲、随机、前瞻性研究,比较在非ST段抬高型心肌梗死(NSTEMI)的ACS患者中,每日三次服用400毫克己酮可可碱并联合标准治疗与标准治疗加安慰剂的效果。ACS患者被随机分为两组,一组接受标准治疗加安慰剂(A组;阿司匹林、氯吡格雷或替格瑞洛、他汀类药物),另一组(B组)在标准治疗基础上加用每日三次400毫克己酮可可碱。主要结局指标是1年时主要不良心血管事件(MACE)的发生率。共有500例患者接受随机分组(250例分配至A组,250例分配至B组),并进行了中位时间为20个月的随访。患者的平均年龄为62.3±10.3岁,80.4%为男性,20.8%患有糖尿病,49.4%患有高血压,42%目前仍在吸烟。对A组的209例患者和B组的210例患者(在因停用研究药物而退出研究的患者之后)进行了统计分析。B组患者中12.38%(n = 26)发生了主要终点事件,而A组为15.78%(n = 33)[相对危险度(RR),0.78;95%置信区间(CI),0.486 - 1.263;P = 0.40],包括心血管死亡(RR,0.93;95% CI,0.48 - 1.80,P = 0.84)、非致命性心肌梗死(RR,1.1;95% CI,0.39 - 3.39,P = 0.78)、中风(RR,0.99;95% CI,0.14 - 6.99,P = 0.99)和冠状动脉血运重建(RR,0.12;95% CI,0.015 - 0.985,P = 0.048)。因此,在ACS患者的标准治疗中加用己酮可可碱并不能改善1年时的MACE,但对冠状动脉血运重建的需求有一定益处。