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Bone markers and cardiovascular risk in type 2 diabetes patients

BACKGROUND: Vascular calcifications are associated with a three- to fourfold increased risk of cardiovascular disease (CVD) and are highly prevalent in type 2 diabetes patients. Emerging evidence indicates that vascular calcification is a process of active bone formation regulated by stimulators and...

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Autores principales: Zwakenberg, Sabine R., van der Schouw, Yvonne T., Schalkwijk, Casper G., Spijkerman, Annemieke M. W., Beulens, Joline W. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866514/
https://www.ncbi.nlm.nih.gov/pubmed/29571288
http://dx.doi.org/10.1186/s12933-018-0691-2
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author Zwakenberg, Sabine R.
van der Schouw, Yvonne T.
Schalkwijk, Casper G.
Spijkerman, Annemieke M. W.
Beulens, Joline W. J.
author_facet Zwakenberg, Sabine R.
van der Schouw, Yvonne T.
Schalkwijk, Casper G.
Spijkerman, Annemieke M. W.
Beulens, Joline W. J.
author_sort Zwakenberg, Sabine R.
collection PubMed
description BACKGROUND: Vascular calcifications are associated with a three- to fourfold increased risk of cardiovascular disease (CVD) and are highly prevalent in type 2 diabetes patients. Emerging evidence indicates that vascular calcification is a process of active bone formation regulated by stimulators and inhibitors of calcification. Therefore, this study aimed to evaluate whether six bone markers are associated with CVD risk in patients with type 2 diabetes. METHODS: We used data of a case-cohort study, nested in the EPIC-NL cohort, comprising 134 CVD cases and a random subcohort of 218 participants, all with type 2 diabetes at baseline. Six bone markers (osteocalcin, osteopontin, osteonectin, osteoprotegerin, alkaline phosphatase and sclerostin) were measured in baseline plasma samples with multiplex assays and information on CVD events was obtained. The association of bone makers with CVD risk was evaluated using Cox proportional hazard analyses. RESULTS: Higher concentrations of plasma osteopontin were associated (p(trend) < 0.01) with an increased CVD risk with a hazard ratio of 2.00 (95%-CI 1.20–3.35) for the highest versus the lowest quartile in a multivariable adjusted model. The other bone markers were not associated with CVD risk. CONCLUSIONS: Higher osteopontin concentrations were associated with an increased CVD risk in type 2 diabetes patients. No consistent associations were found for the other five bone markers and risk of CVD in type 2 diabetes patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12933-018-0691-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-58665142018-03-28 Bone markers and cardiovascular risk in type 2 diabetes patients Zwakenberg, Sabine R. van der Schouw, Yvonne T. Schalkwijk, Casper G. Spijkerman, Annemieke M. W. Beulens, Joline W. J. Cardiovasc Diabetol Original Investigation BACKGROUND: Vascular calcifications are associated with a three- to fourfold increased risk of cardiovascular disease (CVD) and are highly prevalent in type 2 diabetes patients. Emerging evidence indicates that vascular calcification is a process of active bone formation regulated by stimulators and inhibitors of calcification. Therefore, this study aimed to evaluate whether six bone markers are associated with CVD risk in patients with type 2 diabetes. METHODS: We used data of a case-cohort study, nested in the EPIC-NL cohort, comprising 134 CVD cases and a random subcohort of 218 participants, all with type 2 diabetes at baseline. Six bone markers (osteocalcin, osteopontin, osteonectin, osteoprotegerin, alkaline phosphatase and sclerostin) were measured in baseline plasma samples with multiplex assays and information on CVD events was obtained. The association of bone makers with CVD risk was evaluated using Cox proportional hazard analyses. RESULTS: Higher concentrations of plasma osteopontin were associated (p(trend) < 0.01) with an increased CVD risk with a hazard ratio of 2.00 (95%-CI 1.20–3.35) for the highest versus the lowest quartile in a multivariable adjusted model. The other bone markers were not associated with CVD risk. CONCLUSIONS: Higher osteopontin concentrations were associated with an increased CVD risk in type 2 diabetes patients. No consistent associations were found for the other five bone markers and risk of CVD in type 2 diabetes patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12933-018-0691-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-23 /pmc/articles/PMC5866514/ /pubmed/29571288 http://dx.doi.org/10.1186/s12933-018-0691-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Zwakenberg, Sabine R.
van der Schouw, Yvonne T.
Schalkwijk, Casper G.
Spijkerman, Annemieke M. W.
Beulens, Joline W. J.
Bone markers and cardiovascular risk in type 2 diabetes patients
title Bone markers and cardiovascular risk in type 2 diabetes patients
title_full Bone markers and cardiovascular risk in type 2 diabetes patients
title_fullStr Bone markers and cardiovascular risk in type 2 diabetes patients
title_full_unstemmed Bone markers and cardiovascular risk in type 2 diabetes patients
title_short Bone markers and cardiovascular risk in type 2 diabetes patients
title_sort bone markers and cardiovascular risk in type 2 diabetes patients
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866514/
https://www.ncbi.nlm.nih.gov/pubmed/29571288
http://dx.doi.org/10.1186/s12933-018-0691-2
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