Tan K T, Tayebjee M H, Lim H S, Lip G Y H
Haemostasis Thrombosis and Vascular Biology Unit, University Department of Medicine City Hospital, Birmingham, UK.
Diabet Med. 2005 Dec;22(12):1657-62. doi: 10.1111/j.1464-5491.2005.01707.x.
The commonest cause of mortality in patients with Type 2 diabetes is atherothrombosis, which can be related to abnormalities in the coagulation and fibrinolytic pathways, as well as in platelet function. Platelet microparticles (PMPs) may contribute to the prothrombotic state and may promote the progression of atherosclerosis. We hypothesized that PMPs are elevated in Type 2 diabetes and that patients with Type 2 diabetes and clinically apparent atherosclerosis would have the highest levels. Similarly, we hypothesized that soluble plasma P-selectin (sPsel) and CD40L (both molecules which are released by activated platelets), as well as %CD62P (P-selectin) and %CD63 positivity on platelets quantified by flow cytometry, would be highest in patients with Type 2 diabetes and clinically apparent atherosclerotic disease, and might be correlated to PMP levels.
Venous blood was obtained from 21 Type 2 diabetic patients without atherosclerotic complications, 18 diabetic patients with clinically apparent atherosclerotic disease and 21 non-diabetic control subjects. PMPs, as well as %CD62P and %CD63 positivity on platelets, were quantified by flow cytometry. sPsel and CD40L were measured using ELISA.
Patients with Type 2 diabetes and clinically apparent atherosclerotic disease had the highest PMP (P=0.045) and sPsel (P=0.046) levels, compared with patients without complications (who had intermediate PMP levels) and control subjects. Control subjects had the lowest CD40L levels (P<0.001) when compared with patients with Type 2 diabetes, with no difference in sCD40L levels between the two diabetic subgroups. %CD62P and %CD63 positivity did not differ between the groups. PMP levels correlated with %CD62P positivity (P=0.026) but not to %CD63 positivity (P=0.089), sCD40L (P=0.407) or sP-sel (P=0.163); sCD40L levels did not correlate with any other marker of platelet activation.
PMPs are elevated in Type 2 diabetes. In addition, patients with clinically apparent atherosclerosis had the highest levels of PMPs and sPsel. Thus, PMPs may be a marker of symptomatic atherosclerotic vascular disease in Type 2 diabetes, and may both represent a useful risk stratification tool as well as a novel therapeutic target for anti-thrombotic drugs.
2型糖尿病患者最常见的死亡原因是动脉粥样硬化血栓形成,这可能与凝血和纤维蛋白溶解途径以及血小板功能异常有关。血小板微粒(PMPs)可能促成血栓前状态,并可能促进动脉粥样硬化的进展。我们推测2型糖尿病患者的PMPs水平升高,且患有2型糖尿病并伴有临床明显动脉粥样硬化的患者其水平最高。同样,我们推测可溶性血浆P选择素(sPsel)和CD40L(这两种分子均由活化血小板释放),以及通过流式细胞术定量的血小板上的%CD62P(P选择素)和%CD63阳性率,在患有2型糖尿病并伴有临床明显动脉粥样硬化疾病的患者中最高,并且可能与PMPs水平相关。
从21例无动脉粥样硬化并发症的2型糖尿病患者、18例患有临床明显动脉粥样硬化疾病的糖尿病患者和21例非糖尿病对照者中采集静脉血。通过流式细胞术对PMPs以及血小板上的%CD62P和%CD63阳性率进行定量。使用酶联免疫吸附测定法(ELISA)检测sPsel和CD40L。
与无并发症的患者(其PMPs水平处于中等)和对照者相比,患有2型糖尿病并伴有临床明显动脉粥样硬化疾病的患者的PMP(P = 0.045)和sPsel(P = 0.046)水平最高。与2型糖尿病患者相比,对照者的CD40L水平最低(P < 0.001),两个糖尿病亚组之间的sCD40L水平无差异。各组之间的%CD62P和%CD63阳性率无差异。PMPs水平与%CD62P阳性率相关(P = 0.026),但与%CD63阳性率(P = 0.089)、sCD40L(P = 0.407)或sP - sel(P = 0.163)无关;sCD40L水平与血小板活化的任何其他标志物均无相关性。
2型糖尿病患者的PMPs水平升高。此外,患有临床明显动脉粥样硬化的患者的PMPs和sPsel水平最高。因此,PMPs可能是2型糖尿病中有症状动脉粥样硬化血管疾病的标志物,并且可能既是一种有用的风险分层工具,也是抗血栓药物的新型治疗靶点。