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Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification
Vitamin K is considered to be involved in the pathological mechanisms of coronary artery calcification (CAC). Correlation between CAC and plasma vitamin K levels was studied. A total of 103 patients, with at least one coronary risk factor, were studied. CAC was measured using 64-slice multislice com...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465808/ https://www.ncbi.nlm.nih.gov/pubmed/28620475 http://dx.doi.org/10.1017/jns.2016.20 |
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author | Torii, S. Ikari, Y. Tanabe, K. Kakuta, T. Hatori, M. Shioi, A. Okano, T. |
author_facet | Torii, S. Ikari, Y. Tanabe, K. Kakuta, T. Hatori, M. Shioi, A. Okano, T. |
author_sort | Torii, S. |
collection | PubMed |
description | Vitamin K is considered to be involved in the pathological mechanisms of coronary artery calcification (CAC). Correlation between CAC and plasma vitamin K levels was studied. A total of 103 patients, with at least one coronary risk factor, were studied. CAC was measured using 64-slice multislice computed tomography (MSCT) and divided into three groups: none (CAC score = 0; n 25), mild to moderate (0 < CAC score < 400; n 52) and severe (CAC score > 400; n 26). Phylloquinone (PK) and menaquinone (MK)-4 and MK-7 were measured by HPLC-tandem MS. Mean age of patients was 64 (sd 13) years, of which 57 % were male. Median CAC score was 57·2. Median levels of PK, MK-4 and MK-7 were 1·33, 0 and 6·99 ng/ml, showing that MK-7 was the dominant vitamin K in this population. MK-7 showed a significant inverse correlation with uncarboxylated osteocalcin (ucOC, P = 0·014), protein induced by vitamin K absence of antagonist-2 (PIVKA-2, P = 0·013), intact parathyroid hormone (P = 0·007) and bone-specific alkaline phosphatase (P = 0·018). CAC showed an inverse correlation with total circulating uncarboxylated matrix Gla protein (t-ucMGP, P = 0·018) and Hb (P = 0·05), and a positive correlation with age (P < 0·001), creatinine, collagen type 1 cross-linked N-terminal telopeptide (NTX, P = 0·03), pulse wave velocity (P < 0·001) and osteoprotegerin (P < 0·001). However, CAC did not have a significant correlation with plasma levels of PK, MK-4 or MK-7. In conclusion, plasma MK-7, MK-4 or PK level did not show significant correlation with CAC despite the association between plasma vitamin K levels and vitamin K-dependent proteins such as ucOC or PIVKA-2. |
format | Online Article Text |
id | pubmed-5465808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54658082017-06-15 Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification Torii, S. Ikari, Y. Tanabe, K. Kakuta, T. Hatori, M. Shioi, A. Okano, T. J Nutr Sci Research Article Vitamin K is considered to be involved in the pathological mechanisms of coronary artery calcification (CAC). Correlation between CAC and plasma vitamin K levels was studied. A total of 103 patients, with at least one coronary risk factor, were studied. CAC was measured using 64-slice multislice computed tomography (MSCT) and divided into three groups: none (CAC score = 0; n 25), mild to moderate (0 < CAC score < 400; n 52) and severe (CAC score > 400; n 26). Phylloquinone (PK) and menaquinone (MK)-4 and MK-7 were measured by HPLC-tandem MS. Mean age of patients was 64 (sd 13) years, of which 57 % were male. Median CAC score was 57·2. Median levels of PK, MK-4 and MK-7 were 1·33, 0 and 6·99 ng/ml, showing that MK-7 was the dominant vitamin K in this population. MK-7 showed a significant inverse correlation with uncarboxylated osteocalcin (ucOC, P = 0·014), protein induced by vitamin K absence of antagonist-2 (PIVKA-2, P = 0·013), intact parathyroid hormone (P = 0·007) and bone-specific alkaline phosphatase (P = 0·018). CAC showed an inverse correlation with total circulating uncarboxylated matrix Gla protein (t-ucMGP, P = 0·018) and Hb (P = 0·05), and a positive correlation with age (P < 0·001), creatinine, collagen type 1 cross-linked N-terminal telopeptide (NTX, P = 0·03), pulse wave velocity (P < 0·001) and osteoprotegerin (P < 0·001). However, CAC did not have a significant correlation with plasma levels of PK, MK-4 or MK-7. In conclusion, plasma MK-7, MK-4 or PK level did not show significant correlation with CAC despite the association between plasma vitamin K levels and vitamin K-dependent proteins such as ucOC or PIVKA-2. Cambridge University Press 2016-12-29 /pmc/articles/PMC5465808/ /pubmed/28620475 http://dx.doi.org/10.1017/jns.2016.20 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Torii, S. Ikari, Y. Tanabe, K. Kakuta, T. Hatori, M. Shioi, A. Okano, T. Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title | Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title_full | Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title_fullStr | Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title_full_unstemmed | Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title_short | Plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
title_sort | plasma phylloquinone, menaquinone-4 and menaquinone-7 levels and coronary artery calcification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465808/ https://www.ncbi.nlm.nih.gov/pubmed/28620475 http://dx.doi.org/10.1017/jns.2016.20 |
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