Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark ; Faculty of Health Sciences, Aarhus University, Aarhus, Denmark.
PLoS One. 2014 Jan 21;9(1):e85566. doi: 10.1371/journal.pone.0085566. eCollection 2014.
Newly formed platelets are associated with increased aggregation and adverse outcomes in patients with coronary artery disease (CAD). The mechanisms involved in the regulation of platelet turnover in patients with CAD are largely unknown.
To investigate associations between platelet turnover parameters, thrombopoietin and markers of low-grade inflammation in patients with stable CAD. Furthermore, to explore the relationship between platelet turnover parameters and type 2 diabetes, prior myocardial infarction, smoking, age, gender and renal insufficiency.
We studied 581 stable CAD patients. Platelet turnover parameters (immature platelet fraction, immature platelet count, mean platelet volume, platelet distribution width and platelet large cell-ratio) were determined using automated flow cytometry (Sysmex XE-2100). Furthermore, we measured thrombopoietin and evaluated low-grade inflammation by measurement of high-sensitive CRP and interleukin-6.
We found strong associations between the immature platelet fraction, immature platelet count, mean platelet volume, platelet distribution width and platelet large cell ratio (r = 0.61-0.99, p<0.0001). Thrombopoietin levels were inversely related to all of the platelet turnover parameters (r = -0.17--0.25, p<0.0001). Moreover, thrombopoietin levels were significantly increased in patients with diabetes (p = 0.03) and in smokers (p = 0.003). Low-grade inflammation evaluated by high-sensitive CRP correlated significantly, yet weakly, with immature platelet count (r = 0.10, p = 0.03) and thrombopoietin (r = 0.16, p<0.001). Also interleukin-6 correlated with thrombopoietin (r = 0.10, p = 0.02).
In stable CAD patients, thrombopoietin was inversely associated with platelet turnover parameters. Furthermore, thrombopoietin levels were increased in patients with diabetes and in smokers. However, low-grade inflammation did not seem to have a substantial impact on platelet turnover parameters.
新形成的血小板与冠心病(CAD)患者的聚集增加和不良预后有关。CAD 患者血小板更新调节的机制在很大程度上尚不清楚。
研究稳定型 CAD 患者血小板更新参数、血小板生成素与低水平炎症标志物之间的相关性。此外,还探讨了血小板更新参数与 2 型糖尿病、既往心肌梗死、吸烟、年龄、性别和肾功能不全之间的关系。
我们研究了 581 例稳定型 CAD 患者。使用自动化流式细胞术(Sysmex XE-2100)测定血小板更新参数(幼稚血小板分数、幼稚血小板计数、平均血小板体积、血小板分布宽度和血小板大细胞比)。此外,我们还测定了血小板生成素,并通过检测高敏 C 反应蛋白和白细胞介素-6 评估了低水平炎症。
我们发现幼稚血小板分数、幼稚血小板计数、平均血小板体积、血小板分布宽度和血小板大细胞比之间存在很强的相关性(r=0.61-0.99,p<0.0001)。血小板生成素水平与所有血小板更新参数呈负相关(r=-0.17-0.25,p<0.0001)。此外,糖尿病患者(p=0.03)和吸烟者(p=0.003)的血小板生成素水平显著升高。用高敏 C 反应蛋白评估的低水平炎症与幼稚血小板计数(r=0.10,p=0.03)和血小板生成素(r=0.16,p<0.001)呈显著弱相关。白细胞介素-6 与血小板生成素也呈相关(r=0.10,p=0.02)。
在稳定型 CAD 患者中,血小板生成素与血小板更新参数呈负相关。此外,糖尿病患者和吸烟者的血小板生成素水平升高。然而,低水平炎症似乎对血小板更新参数没有实质性影响。