Division of Nephrology, Department of Internal Medicine, Ewha Womans University School of Medicine, Seoul, Korea.
Medical Research Institute, Ewha Womans University School of Medicine, Seoul, Korea.
Kidney Res Clin Pract. 2012 Mar;31(1):38-47. doi: 10.1016/j.krcp.2011.12.002. Epub 2012 Jan 6.
Vascular access failure, a major cause of morbidity in hemodialysis (HD) patients, occurs mainly at stenotic endothelium following an acute thrombotic event. Microparticles (MPs) are fragments derived from injured cell membrane and are closely associated with coagulation and vascular inflammatory responses.
We investigated the relationship between levels of circulating MPs and vascular access patency in HD patients. A total of 82 HD patients and 28 healthy patients were enrolled. We used flow cytometry to measure endothelial MPs (EMPs) identified by CD31+CD42- or CD51+ and platelet-derived MPs (PMPs) identified by CD31+CD42+ in plasma samples of participants. Vascular access patency was defined as an interval from the time of access formation to the time of first access stenosis in each patient. MP counts were compared according to access patent duration.
The levels of EMP (both CD31+CD42- and CD51+) and CD31+CD42+PMP were significantly higher in patients than in healthy participants. Levels of CD31+CD42-EMP and CD31+CD42+PMP showed a positive correlation. In non-diabetic HD patients, CD31+CD42-EMPs and CD31+CD42+PMPs were more elevated in the shorter access survival group (access survival <1 year) than in the longer survival group (access survival ≥ 4 years).
Elevated circulating EMP or PMP counts are influenced by end-stage renal disease and increased levels of EMP and PMP may be associated with vascular access failure in HD patients.
血管通路失功是血液透析(HD)患者发病率升高的主要原因,主要发生在急性血栓事件后狭窄的内皮细胞。微粒(MPs)是来源于损伤细胞膜的碎片,与凝血和血管炎症反应密切相关。
我们研究了 HD 患者循环 MPs 水平与血管通路通畅性之间的关系。共纳入 82 例 HD 患者和 28 例健康对照者。我们采用流式细胞术测量了参与者血浆样本中内皮 MPs(EMP)(CD31+CD42-或 CD51+)和血小板衍生 MPs(PMP)(CD31+CD42+)。血管通路通畅性定义为每位患者从建立通路到首次发生通路狭窄的时间间隔。根据通路持续时间比较 MPs 计数。
与健康对照组相比,患者的 EMP(CD31+CD42-和 CD51+)和 CD31+CD42+PMP 水平显著升高。CD31+CD42-EMP 和 CD31+CD42+PMP 水平呈正相关。在非糖尿病 HD 患者中,较短通路生存组(<1 年)的 CD31+CD42-EMP 和 CD31+CD42+PMP 水平高于较长生存组(≥4 年)。
循环 EMP 或 PMP 计数的升高受终末期肾病的影响,升高的 EMP 和 PMP 水平可能与 HD 患者的血管通路失功有关。