Joseph Jubin P, Reyes Eliana, Guzman Josephine, O'Doherty Jim, McConkey Hannah, Arri Satpal, Kakkar Rahul, Beckley Nicholas, Douiri Abdel, Barrington Sally F, Redwood Simon R, Ferro Albert
British Heart Foundation Centre of Excellence, The Rayne Institute, St. Thomas' Hospital, London, SE1 7EH, UK.
PET Centre, St. Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.
Trials. 2017 Oct 11;18(1):473. doi: 10.1186/s13063-017-2210-2.
There is emerging evidence of the central role of neutrophils in both atherosclerotic plaque formation and rupture. Patients with lower neutrophil counts following acute coronary syndromes tend to have a greater coronary flow reserve, which is a strong predictor of long-term cardiovascular health. But so far, no data are available regarding the impact of neutrophil inhibition on cardiovascular clinical or surrogate endpoints. Therefore, the aim of this study is to investigate the effects of AZD5069, a cysteine-X-cysteine chemokine receptor 2 (CXCR2) inhibitor, on coronary flow reserve and coronary structure and function in patients with coronary artery disease.
METHODS/DESIGN: Ninety subjects with coronary artery disease undergoing percutaneous coronary intervention will be included in this investigator-driven, randomised, placebo-controlled, double-blind, phase IIa, single-centre study. Participants will be randomised to receive either AZD5069 (40 mg) administered orally twice daily or placebo for 24 weeks. Change in coronary flow reserve as determined by N-ammonia positron emission tomography-computed tomography will be the primary outcome. Change in the inflammatory component of coronary plaque structure and the backward expansion wave, an invasive coronary physiological measure of diastolic function, will be assessed as secondary outcomes.
Cardiovascular surrogate parameters, such as coronary flow reserve, may provide insights into the potential mechanisms of the cardiovascular effects of CXCR2 inhibitors. Currently, ongoing trials do not specifically focus on neutrophil function as a target of intervention, and we therefore believe that our study will contribute to a better understanding of the role of neutrophil-mediated inflammation in coronary artery disease.
EudraCT, 2016-000775-24 . Registered on 22 July 2016. International Standard Randomised Controlled Trial Number, ISRCTN48328178 . Registered on 25 February 2016.
越来越多的证据表明中性粒细胞在动脉粥样硬化斑块形成和破裂过程中起核心作用。急性冠状动脉综合征后中性粒细胞计数较低的患者往往具有更大的冠状动脉血流储备,这是长期心血管健康的有力预测指标。但迄今为止,尚无关于中性粒细胞抑制对心血管临床或替代终点影响的数据。因此,本研究的目的是探讨半胱氨酸- X -半胱氨酸趋化因子受体2(CXCR2)抑制剂AZD5069对冠心病患者冠状动脉血流储备以及冠状动脉结构和功能的影响。
方法/设计:本研究为研究者发起的、随机、安慰剂对照、双盲、IIa期、单中心研究,将纳入90例接受经皮冠状动脉介入治疗的冠心病患者。参与者将被随机分配,每日口服两次40毫克AZD5069或安慰剂,持续24周。由N -氨正电子发射断层扫描 - 计算机断层扫描测定的冠状动脉血流储备变化将作为主要结局。冠状动脉斑块结构炎症成分的变化以及舒张功能的侵入性冠状动脉生理指标——逆向扩张波将作为次要结局进行评估。
心血管替代参数,如冠状动脉血流储备,可能有助于深入了解CXCR2抑制剂心血管效应的潜在机制。目前,正在进行的试验并未特别关注将中性粒细胞功能作为干预靶点,因此我们认为本研究将有助于更好地理解中性粒细胞介导的炎症在冠心病中的作用。
欧洲药品管理局临床试验数据库(EudraCT),2016 - 000775 - 24。于2016年7月22日注册。国际标准随机对照试验编号,ISRCTN48328178。于