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      Desphospho-uncarboxylated matrix Gla protein is associated with increased aortic stiffness in a general population.

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          Abstract

          Matrix Gla protein (MGP), a natural inhibitor of calcification, strongly correlates with the extent of coronary calcification. Vitamin K is the essential cofactor for the activation of MGP. The nonphosphorylated-uncarboxylated isoform of MGP (dp-ucMGP) reflects the status of this vitamin. We investigated whether there is an association between dp-ucMGP and stiffness of elastic and muscular-type large arteries in a random sample from the general population. In a cross-sectional design, we analyzed 1087 subjects from the Czech post-MONICA study. Aortic and femoro-popliteal pulse wave velocities (PWVs) were measured using a Sphygmocor device. Dp-ucMGP concentrations were assessed in freshly frozen samples by enzyme-linked immunosorbent assay methods using the InaKtif MGP iSYS pre-commercial kit developed by IDS and VitaK. Aortic PWV significantly (P<0.0001) increased across the dp-ucMGP quartiles. After adjustment for all potential confounders, aortic PWV independently correlated with dp-ucMGP (with beta coefficient (s.d.) 11.61 (5.38) and P-value=0.031). In a categorized manner, subjects in the top quartile of dp-ucMGP (⩾ 671 pmol l(-1)) had a higher risk of elevated aortic PWV, with corresponding adjusted odds ratio (95% confidence interval) 1.73 (1.17-2.5). In contrast, no relation between dp-ucMGP and femoro-popliteal PWV was found. In conclusion, increased dp-ucMGP, which is a circulating biomarker of vitamin K status and vascular calcification, is independently associated with aortic stiffness, but not with stiffness of distal muscular-type arteries.

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          Author and article information

          Journal
          J Hum Hypertens
          Journal of human hypertension
          1476-5527
          0950-9240
          Jul 2016
          : 30
          : 7
          Affiliations
          [1 ] 2nd Department of Internal Medicine, Medical Faculty of Charles University and University Hospital, Pilsen, Czech Republic.
          [2 ] Biomedical Centre, Medical Faculty of Charles University, Pilsen, Czech Republic.
          [3 ] Centre for Cardiovascular Prevention of the First Faculty of Medicine, Charles University and Thomayer Hospital, Prague, Czech Republic.
          [4 ] International Clinical Research Centre, St. Anne's University Hospital, Brno, Czech Republic.
          [5 ] Department of Immunodiagnostics, University Hospital, Pilsen, Czech Republic.
          [6 ] VitaK, Cardiovascular Research Institute, Maastricht University, Maastricht, The Netherlands.
          Article
          jhh201555
          10.1038/jhh.2015.55
          26016598
          32074e27-e33b-4afe-8e41-faede3b0bbb1
          History

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