Department of Clinical and Experimental Medicine, Federico II University Medical School, Naples, Italy.
Nephrol Dial Transplant. 2011 Jul;26(7):2264-70. doi: 10.1093/ndt/gfq733. Epub 2011 Jan 10.
Venous neointimal hyperplasia is the most common cause of arteriovenous (AV) fistula and graft dysfunction following dialysis access surgery. However, the pathogenetic impact of pre-existing venous neointimal hyperplasia at the time of AV access creation on final clinical success is currently unknown in the setting of advanced chronic kidney disease (CKD) and end-stage renal disease (ESRD) patients. The aim of this study was to perform a detailed histological, morphometric, and immunohistochemical analysis of vein specimens in advanced CKD and ESRD patients collected at the time of new vascular access placement.
Vein samples from 12 patients were collected at the time of AV access creation near the site of AV anastomosis. Histological, immunohistochemistry and morphometric studies were performed on these vein samples.
Examination of the tissue specimens obtained at the time of surgery showed neointimal hyperplasia in 10 of 12 specimens, ranging from minimal to very severe. The majority of cells within the neointima were myofibroblasts with a minority of contractile smooth muscle cells present.
Our work represents a detailed description of the morphometric and cellular phenotypic lesions present in the veins of CKD and ESRD patients, prior to dialysis access placement. These studies (i) suggest the future possibility of a new predictive marker (pre-existing venous neointimal hyperplasia) for AV dialysis access dysfunction and (ii) open the door for the future development of novel local therapies for optimization of the venous substrate on which the dialysis access is created.
静脉性内膜增生是透析通路手术后动静脉(AV)瘘和移植物功能障碍的最常见原因。然而,在晚期慢性肾脏病(CKD)和终末期肾病(ESRD)患者中,AV 通路创建时存在的静脉性内膜增生对最终临床成功的发病机制影响目前尚不清楚。本研究旨在对新血管通路放置时收集的晚期 CKD 和 ESRD 患者静脉标本进行详细的组织学、形态计量学和免疫组织化学分析。
在 AV 吻合口附近 AV 通路创建时收集 12 名患者的静脉样本。对这些静脉样本进行组织学、免疫组织化学和形态计量学研究。
手术时获得的组织标本检查显示,12 个标本中有 10 个存在内膜增生,从轻度到重度不等。新生内膜中的大多数细胞是肌成纤维细胞,少数存在收缩性平滑肌细胞。
我们的工作代表了对 CKD 和 ESRD 患者静脉中存在的形态计量学和细胞表型病变的详细描述,这些病变发生在透析通路放置之前。这些研究表明(i)未来可能会出现一种新的预测标志物(预先存在的静脉性内膜增生),用于预测 AV 透析通路功能障碍;(ii)为未来开发优化透析通路所创建的静脉基质的新型局部治疗方法开辟了道路。