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Uremic Toxins Affecting Cardiovascular Calcification: A Systematic Review

Overview
Journal Cells
Publisher MDPI
Date 2020 Nov 11
PMID 33172085
Citations 12
Authors
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Abstract

Cardiovascular calcification is highly prevalent and associated with increased morbidity in chronic kidney disease (CKD). This review examines the impact of uremic toxins, which accumulate in CKD due to a failing kidney function, on cardiovascular calcification. A systematic literature search identified 41 uremic toxins that have been studied in relation to cardiovascular calcification. For 29 substances, a potentially causal role in cardiovascular calcification was addressed in in vitro or animal studies. A calcification-inducing effect was revealed for 16 substances, whereas for three uremic toxins, namely the guanidino compounds asymmetric and symmetric dimethylarginine, as well as guanidinosuccinic acid, a calcification inhibitory effect was identified in vitro. At a mechanistic level, effects of uremic toxins on calcification could be linked to the induction of inflammation or oxidative stress, smooth muscle cell osteogenic transdifferentiation and/or apoptosis, or alkaline phosphatase activity. For all middle molecular weight and protein-bound uremic toxins that were found to affect cardiovascular calcification, an increasing effect on calcification was revealed, supporting the need to focus on an increased removal efficiency of these uremic toxin classes in dialysis. In conclusion, of all uremic toxins studied with respect to calcification regulatory effects to date, more uremic toxins promote rather than reduce cardiovascular calcification processes. Additionally, it highlights that only a relatively small part of uremic toxins has been screened for effects on calcification, supporting further investigation of uremic toxins, as well as of associated post-translational modifications, on cardiovascular calcification processes.

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References
1.
Lesaffer G, De Smet R, Lameire N, DHondt A, Duym P, Vanholder R . Intradialytic removal of protein-bound uraemic toxins: role of solute characteristics and of dialyser membrane. Nephrol Dial Transplant. 1999; 15(1):50-7. DOI: 10.1093/ndt/15.1.50. View

2.
Brettschneider F, Tolle M, von der Giet M, Passlick-Deetjen J, Steppan S, Peter M . Removal of protein-bound, hydrophobic uremic toxins by a combined fractionated plasma separation and adsorption technique. Artif Organs. 2013; 37(4):409-16. DOI: 10.1111/j.1525-1594.2012.01570.x. View

3.
Sage A, Lu J, Tintut Y, Demer L . Hyperphosphatemia-induced nanocrystals upregulate the expression of bone morphogenetic protein-2 and osteopontin genes in mouse smooth muscle cells in vitro. Kidney Int. 2010; 79(4):414-22. PMC: 3198856. DOI: 10.1038/ki.2010.390. View

4.
Zickler D, Luecht C, Willy K, Chen L, Witowski J, Girndt M . Tumour necrosis factor-alpha in uraemic serum promotes osteoblastic transition and calcification of vascular smooth muscle cells via extracellular signal-regulated kinases and activator protein 1/c-FOS-mediated induction of interleukin 6 expression. Nephrol Dial Transplant. 2017; 33(4):574-585. DOI: 10.1093/ndt/gfx316. View

5.
Madero M, Cano K, Campos I, Tao X, Maheshwari V, Brown J . Removal of Protein-Bound Uremic Toxins during Hemodialysis Using a Binding Competitor. Clin J Am Soc Nephrol. 2019; 14(3):394-402. PMC: 6419294. DOI: 10.2215/CJN.05240418. View