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本文引用的文献

1
Assessment of the association between increasing membrane pore size and endotoxin permeability using a novel experimental dialysis simulation set-up.使用新型实验透析模拟装置评估膜孔径增大与内毒素通透性之间的关联。
BMC Nephrol. 2018 Jan 5;19(1):1. doi: 10.1186/s12882-017-0808-y.
2
Modulation of leucocytic angiotensin-converting enzymes expression in patients maintained on high-permeable haemodialysis.高通量血液透析患者白细胞血管紧张素转换酶表达的调节。
Nephrol Dial Transplant. 2018 Jan 1;33(1):34-43. doi: 10.1093/ndt/gfx206.
3
Membrane Innovation in Dialysis.透析中的膜创新
Contrib Nephrol. 2017;191:100-114. doi: 10.1159/000479259. Epub 2017 Sep 14.
4
Comparison of hemodialysis with medium cut-off dialyzer and on-line hemodiafiltration on the removal of small and middle-sized molecules
.采用中截流透析器的血液透析与在线血液透析滤过对中小分子清除效果的比较
Clin Nephrol. 2018 Jan;89 (2018)(1):50-56. doi: 10.5414/CN109133.
5
In Vitro Dialysis of Cytokine-Rich Plasma With High and Medium Cut-Off Membranes Reduces Its Procalcific Activity.使用高截留和中截留膜对富含细胞因子的血浆进行体外透析可降低其促钙化活性。
Artif Organs. 2017 Sep;41(9):803-809. doi: 10.1111/aor.12884. Epub 2017 May 19.
6
Developing a Set of Core Outcomes for Trials in Hemodialysis: An International Delphi Survey.制定血液透析试验的核心结局集:一项国际德尔菲调查。
Am J Kidney Dis. 2017 Oct;70(4):464-475. doi: 10.1053/j.ajkd.2016.11.029. Epub 2017 Feb 24.
7
Medium Cut-Off (MCO) Membranes Reduce Inflammation in Chronic Dialysis Patients-A Randomized Controlled Clinical Trial.中截流(MCO)膜可减轻慢性透析患者的炎症——一项随机对照临床试验
PLoS One. 2017 Jan 13;12(1):e0169024. doi: 10.1371/journal.pone.0169024. eCollection 2017.
8
Performance of hemodialysis with novel medium cut-off dialyzers.新型中截留量透析器的血液透析性能
Nephrol Dial Transplant. 2017 Jan 1;32(1):165-172. doi: 10.1093/ndt/gfw310.
9
High cut-off dialysis in chronic haemodialysis patients reduces serum procalcific activity.高通量透析降低慢性血液透析患者的血清钙化活性。
Nephrol Dial Transplant. 2016 Oct;31(10):1706-12. doi: 10.1093/ndt/gfw293. Epub 2016 Jul 20.
10
FGF23 signaling impairs neutrophil recruitment and host defense during CKD.在慢性肾脏病期间,成纤维细胞生长因子23(FGF23)信号传导会损害中性粒细胞募集和宿主防御功能。
J Clin Invest. 2016 Mar 1;126(3):962-74. doi: 10.1172/JCI83470. Epub 2016 Feb 15.

探讨增加大中分子清除的临床意义。

Exploring the Clinical Relevance of Providing Increased Removal of Large Middle Molecules.

机构信息

Department of Renal Medicine, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.

Faculty of Medicine, University of Queensland, Brisbane, Queensland, Australia.

出版信息

Clin J Am Soc Nephrol. 2018 May 7;13(5):805-814. doi: 10.2215/CJN.10110917. Epub 2018 Mar 5.

DOI:10.2215/CJN.10110917
PMID:29507008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5969479/
Abstract

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.

摘要

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。