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Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes
BACKGROUND: We aimed to investigate the bone turnover markers in coronary artery disease (CAD) patients with and without type 2 diabetes (T2DM) in comparison with control subjects without CAD and T2DM. METHODS: This cross-sectional study was performed on 45 subjects undergoing elective heart surgery...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012061/ https://www.ncbi.nlm.nih.gov/pubmed/27602333 http://dx.doi.org/10.1186/s40200-016-0259-1 |
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author | Maghbooli, Zhila Emamgholipour, Solaleh Hossein-nezhad, Arash Shirzad, Mahmood Gorgani Firuzjaee, Sattar |
author_facet | Maghbooli, Zhila Emamgholipour, Solaleh Hossein-nezhad, Arash Shirzad, Mahmood Gorgani Firuzjaee, Sattar |
author_sort | Maghbooli, Zhila |
collection | PubMed |
description | BACKGROUND: We aimed to investigate the bone turnover markers in coronary artery disease (CAD) patients with and without type 2 diabetes (T2DM) in comparison with control subjects without CAD and T2DM. METHODS: This cross-sectional study was performed on 45 subjects undergoing elective heart surgery; either for coronary artery bypass grafting or for valve surgery. According to angiographic results, participants were grouped in two groups with CAD (n = 33) and without CAD (n = 12). The serum levels of osteocalcin (OC), procollagen I aminoterminal propeptide (P1NP) and carboxy-terminal collagen crosslinks (CTX), as bone turnover markers, as well as serum levels of 25 (OH) vitamin D3, PTH, and common metabolic factors were analyzed in all participants. RESULTS: Serum levels of bone markers did not differ in patients with CAD compared to non-CAD subjects. Regarding metabolic factors, serum levels of FBG had invert correlation with OC in CAD patients (p = 0.004). The data of subgroup analysis showed serum levels of OC and CTX were statistically significant lower in CAD-DM than CAD-non DM (p < 0.05). There were not any significant differences in the P1NP levels between groups. CONCLUSIONS: Our data suggest that CTX and OC would be used as suitable bone markers in CAD patients with T2DM. However, further clinical studies need to establish the role of these markers in CAD patients with diabetes. |
format | Online Article Text |
id | pubmed-5012061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50120612016-09-07 Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes Maghbooli, Zhila Emamgholipour, Solaleh Hossein-nezhad, Arash Shirzad, Mahmood Gorgani Firuzjaee, Sattar J Diabetes Metab Disord Research Article BACKGROUND: We aimed to investigate the bone turnover markers in coronary artery disease (CAD) patients with and without type 2 diabetes (T2DM) in comparison with control subjects without CAD and T2DM. METHODS: This cross-sectional study was performed on 45 subjects undergoing elective heart surgery; either for coronary artery bypass grafting or for valve surgery. According to angiographic results, participants were grouped in two groups with CAD (n = 33) and without CAD (n = 12). The serum levels of osteocalcin (OC), procollagen I aminoterminal propeptide (P1NP) and carboxy-terminal collagen crosslinks (CTX), as bone turnover markers, as well as serum levels of 25 (OH) vitamin D3, PTH, and common metabolic factors were analyzed in all participants. RESULTS: Serum levels of bone markers did not differ in patients with CAD compared to non-CAD subjects. Regarding metabolic factors, serum levels of FBG had invert correlation with OC in CAD patients (p = 0.004). The data of subgroup analysis showed serum levels of OC and CTX were statistically significant lower in CAD-DM than CAD-non DM (p < 0.05). There were not any significant differences in the P1NP levels between groups. CONCLUSIONS: Our data suggest that CTX and OC would be used as suitable bone markers in CAD patients with T2DM. However, further clinical studies need to establish the role of these markers in CAD patients with diabetes. BioMed Central 2016-09-06 /pmc/articles/PMC5012061/ /pubmed/27602333 http://dx.doi.org/10.1186/s40200-016-0259-1 Text en © The Author(s). 2016 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 | Research Article Maghbooli, Zhila Emamgholipour, Solaleh Hossein-nezhad, Arash Shirzad, Mahmood Gorgani Firuzjaee, Sattar Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title | Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title_full | Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title_fullStr | Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title_full_unstemmed | Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title_short | Suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
title_sort | suitable bone markers assessing bone status in patients with both coronary artery disease and diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5012061/ https://www.ncbi.nlm.nih.gov/pubmed/27602333 http://dx.doi.org/10.1186/s40200-016-0259-1 |
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