Saritas T, Reinartz S, Krueger T, Ketteler M, Liangos O, Labriola L, Stenvinkel P, Kopp C, Westenfeld R, Evenepoel P, Siepmann R, Wied S, Hilgers RD, Schurgers L, Floege J (2022)
Publication Type: Journal article
Publication year: 2022
DOI: 10.1093/ckj/sfac184
Lay Summary Patients on chronic dialysis exhibit extensive cardiovascular calcifications and vitamin K deficiency. The vitamin K-dependent matrix Gla protein (MGP) is a potent inhibitor of vascular calcification. The multicentre, randomized, open-label, controlled VitaVasK trial showed marked attenuation of cardiovascular calcification progression in chronic haemodialysis patients treated with vitamin K1. Vitamin K1 supplementation greatly increased the serum vitamin K concentration and reduced inactive MGP levels. The treatment was safe, as no adverse advents were noted. Larger randomized controlled trials are needed to confirm vitamin K1 therapy as a safe, potent and cost-effective treatment option to reduce the progression of vascular calcification in haemodialysis patients.
APA:
Saritas, T., Reinartz, S., Krueger, T., Ketteler, M., Liangos, O., Labriola, L.,... Floege, J. (2022). Vitamin K1 and progression of cardiovascular calcifications in hemodialysis patients: the VitaVasK randomized controlled trial. Clinical Kidney Journal. https://doi.org/10.1093/ckj/sfac184
MLA:
Saritas, Turgay, et al. "Vitamin K1 and progression of cardiovascular calcifications in hemodialysis patients: the VitaVasK randomized controlled trial." Clinical Kidney Journal (2022).
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