Division of Angiology, Department of Internal Medicine II, Medical University of Vienna, Austria.
Swiss Med Wkly. 2013 May 28;143:w13800. doi: 10.4414/smw.2013.13800. eCollection 2013.
Atherosclerosis affects many patients with type 2 diabetes. Both are associated with platelet activation, but it remains unclear how diabetes contributes to, or even enhances, platelet activation in patients with atherosclerosis. We therefore investigated the impact of diabetes on platelet activation and protease activated receptor-1 (PAR-1) mediated platelet response in patients with symptomatic coronary artery disease (CAD), as compared with other manifestations of atherosclerosis.
Baseline P-selectin expression, thrombin receptor activating peptide-6 (TRAP-6) inducible P-selectin, and relative increase of platelet P-selectin after activation with TRAP-6 were measured using flow cytometry in platelets from 317 patients after angioplasty and stenting for symptomatic atherosclerotic disease, and from 50 healthy controls.
Patients with symptomatic atherosclerosis exhibited significantly higher levels of baseline P-selectin expression, TRAP-6-inducible P-selectin and relative increase of platelet P-selectin after stimulation with TRAP-6 than healthy controls. Patients with symptomatic peripheral artery disease or cerebrovascular disease (PAD/CVD) had higher levels of platelet activation and PAR-1-mediated platelet reactivity than patients with symptomatic CAD. Of interest, CAD patients with diabetes responded more strongly to TRAP-6 than those without diabetes, and their platelet activation and PAR-1-mediated platelet reactivity resembled those from PAD/CVD patients.
Compared with healthy controls, platelets from patients with symptomatic atherosclerotic disease are activated and susceptible to PAR-1-mediated activation. Diabetes affects platelet reactivity only in patients with symptomatic CAD, while other manifestations of atherosclerosis may have an overwhelming effect on platelet reactivity that is not further enhanced by diabetes.
动脉粥样硬化影响许多 2 型糖尿病患者。两者都与血小板激活有关,但糖尿病如何导致甚至增强动脉粥样硬化患者的血小板激活仍不清楚。因此,我们研究了糖尿病对有症状的冠心病(CAD)患者血小板激活和蛋白酶激活受体-1(PAR-1)介导的血小板反应的影响,并与动脉粥样硬化的其他表现进行了比较。
使用流式细胞术测量了 317 例经血管成形术和支架置入治疗有症状动脉粥样硬化疾病患者及 50 例健康对照者的血小板中基础 P-选择素表达、血栓素受体激活肽-6(TRAP-6)诱导的 P-选择素以及用 TRAP-6 激活后血小板 P-选择素的相对增加。
与健康对照组相比,有症状动脉粥样硬化患者的基础 P-选择素表达、TRAP-6 诱导的 P-选择素和用 TRAP-6 刺激后血小板 P-选择素的相对增加均显著升高。有症状外周动脉疾病或脑血管疾病(PAD/CVD)的患者的血小板激活和 PAR-1 介导的血小板反应性高于有症状 CAD 的患者。有趣的是,有糖尿病的 CAD 患者对 TRAP-6 的反应强于无糖尿病的患者,其血小板激活和 PAR-1 介导的血小板反应性类似于 PAD/CVD 患者。
与健康对照组相比,有症状动脉粥样硬化疾病患者的血小板被激活且易受 PAR-1 介导的激活。糖尿病仅影响有症状 CAD 患者的血小板反应性,而动脉粥样硬化的其他表现可能对血小板反应性有压倒性的影响,糖尿病不会进一步增强这种反应性。