Ahmed Syed, Roy-Chaudhury Prabir
Dialysis Vascular Access Research Group, Division of Nephrology, University of Cincinnati, Cincinnati, Ohio 45267-0585, USA.
Semin Dial. 2012 Jul;25(4):464-9. doi: 10.1111/j.1525-139X.2011.01006.x. Epub 2012 Jan 25.
Hemodialysis vascular access dysfunction is a major cause of morbidity and hospitalization in the hemodialysis population at a cost of well over $1 billion per annum. Venous stenosis (due to venous neointimal hyperplasia [VNH]) is the most common cause of polytetrafluroethylene PTFE) dialysis access graft and arteriovenous fistula (AVF) failure. Despite the magnitude of the clinical problem, however, there are currently no effective therapies for this condition. We and others have previously demonstrated that VNH in PTFE dialysis grafts and AVF is composed of smooth muscle cells/myofibroblasts, endothelial cells within neointimal microvessels, and peri-graft macrophages. Radiation therapy blocks the proliferation and activation of all these cell types. The current review will dissect out the available in vitro, experimental, and clinical data on the use of radiation therapy for vascular stenosis in general, and for dialysis access dysfunction in particular. It is important to try and identify whether there is still a role for radiation therapy in this specific clinical setting. We believe that this is a critically important question to answer in view of the huge unmet clinical need that is currently associated with hemodialysis vascular access dysfunction.
血液透析血管通路功能障碍是血液透析人群发病和住院的主要原因,每年花费超过10亿美元。静脉狭窄(由于静脉内膜增生[VNH])是聚四氟乙烯(PTFE)透析通路移植物和动静脉内瘘(AVF)失败的最常见原因。然而,尽管这一临床问题严重,但目前尚无针对该病症的有效治疗方法。我们和其他人之前已经证明,PTFE透析移植物和AVF中的VNH由平滑肌细胞/肌成纤维细胞、新内膜微血管内的内皮细胞以及移植物周围的巨噬细胞组成。放射治疗可阻断所有这些细胞类型的增殖和活化。本综述将剖析关于一般血管狭窄,特别是透析通路功能障碍使用放射治疗的现有体外、实验和临床数据。尝试确定放射治疗在这一特定临床环境中是否仍有作用很重要。鉴于目前与血液透析血管通路功能障碍相关的巨大未满足临床需求,我们认为这是一个至关重要的需要回答的问题。