| Literature DB >> 26130027 |
Maria Fusaro1, Sandro Giannini2, Maurizio Gallieni3, Marianna Noale4, Giovanni Tripepi5, Maurizio Rossini6, Piergiorgio Messa7, Paolo Rigotti8, Tecla Pati9, Francesco Barbisoni10, Antonio Piccoli11, Andrea Aghi11, Marianna Alessi11, Luciana Bonfante11, Fabrizio Fabris2, Sabina Zambon2, Stefania Sella2, Giorgio Iervasi12, Mario Plebani13.
Abstract
Matrix Gla protein (MGP) and bone Gla protein (BGP) are two vitamin K-dependent proteins (VKDPs) involved in the regulation of vascular calcification (VC). We carried out a secondary analysis of the VIKI study to evaluate associations between drug consumption and VKDP levels in 387 hemodialyzed patients. The VIKI study assessed the prevalence of vitamin K deficiency in hemodialysis patients. We evaluated drug consumption, determined BGP and MGP levels, and verified the presence of any vertebral fractures (VF) and VC by spine radiographs. Total BGP levels were twice as high with calcimimetics versus no calcimimetics (290 vs. 158.5 mcg/L, p < 0.0001) and 69 % higher with vitamin D analogs (268 vs. 159 mcg/L, p < 0.0001). Total MGP was 19 % higher with calcimimetics (21.5 vs. 18.1 mcg/L, p = 0.04) and 54 % higher with calcium acetate (27.9 vs. 18.1 mcg/L, p = 0.003); no difference was found with vitamin D analogs (21.1 vs. 18.3 mcg/L, p = 0.43). Median Total BGP level was 29 % lower in patients with ≥1 VF (151 vs. 213 mcg/L, p = 0.0091) and 36 % lower in patients with VC (164 vs. 262.1 mcg/L, p = 0.0003). In non-survivors, median BGP and MGP were lower, but only for MGP this difference reached the statistical significance (152 vs. 191 mcg/L, p = 0.20 and 15.0 vs. 19.7 mcg/L, p = 0.02, respectively). Pending studies on vitamin K supplementation, calcimimetics, and vitamin D analogs may play a role in preserving vitamin K-dependent protein activity, thus contributing to bone and vascular health in CKD patients.Entities:
Keywords: Biochemical markers of bone turnover; CKD; Matrix mineralization; Vascular calcification; Vitamin K proteins
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Year: 2015 PMID: 26130027 DOI: 10.1007/s12020-015-0673-z
Source DB: PubMed Journal: Endocrine ISSN: 1355-008X Impact factor: 3.633