Department of Renal Medicine, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.
Clin J Am Soc Nephrol. 2018 May 7;13(5):805-814. doi: 10.2215/CJN.10110917. Epub 2018 Mar 5.
Dialysis technologies have continued to advance over recent decades; however, these advancements have not always been met with improved patient outcomes. In part, the high morbidity and mortality associated with dialysis have been attributed to a group of uremic toxins, which are described as "difficult to remove." With a new generation of hemodialysis membranes now making meaningful clearance of these molecules possible, it is an apt time to review the clinical relevance of these middle molecules. Our review describes the developments in membrane technology that enable the removal of large middle molecules (molecular mass >15 kD) that is limited with high-flux dialysis membranes. Of the known 58 middle molecules, a literature search identified 27 that have molecular mass >15 kD. This group contains cytokines, adipokines, hormones, and other proteins. These molecules are implicated in chronic inflammation, atherosclerosis, structural heart disease, and secondary immunodeficiency in the literature. Single-center safety and efficacy studies have identified that use of these membranes in maintenance dialysis populations is associated with limited loss of albumin and increased clearance of large middle molecules. Larger, robustly conducted, multicenter studies are now evaluating these findings. After completion of these safety and efficacy studies, the perceived clinical benefits of providing clearance of large middle molecules must be assessed in rigorously conducted, randomized clinical studies.
在过去的几十年中,透析技术不断进步;然而,这些进步并不总是伴随着改善的患者预后。部分原因是,与透析相关的高发病率和死亡率归因于一组尿毒症毒素,这些毒素被描述为“难以清除”。随着新一代血液透析膜现在可以实现这些分子的有意义清除,现在正是回顾这些中分子的临床相关性的好时机。我们的综述描述了膜技术的发展,这些发展使得能够清除高通量透析膜有限的大分子量(分子量> 15 kD)的中间分子。在已知的 58 种中间分子中,文献检索确定了 27 种分子量> 15 kD 的中间分子。这一组包含细胞因子、脂肪因子、激素和其他蛋白质。这些分子在文献中与慢性炎症、动脉粥样硬化、结构性心脏病和继发性免疫缺陷有关。单中心安全性和疗效研究表明,在维持性透析人群中使用这些膜与白蛋白有限丢失和大分子量中间分子清除增加有关。更大规模、更严格进行的多中心研究目前正在评估这些发现。在这些安全性和疗效研究完成后,必须在严格进行的随机临床试验中评估提供大分子量中间分子清除的潜在临床益处。