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Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients

BACKGROUND: Myeloid-related protein 8/14 (MRP8/14) is a stable heterodimer formed by two different calcium-binding proteins (MRP8 and MRP14). Studies have identified that MRP8/14 regulates vascular inflammation and serves as a novel marker of acute coronary syndrome. In this study, we evaluated the...

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Autores principales: Peng, Wen Hui, Jian, Wei Xia, Li, Hai Ling, Hou, Lei, Wei, Yi Dong, Li, Wei Ming, Xu, Ya Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120649/
https://www.ncbi.nlm.nih.gov/pubmed/21592353
http://dx.doi.org/10.1186/1475-2840-10-41
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author Peng, Wen Hui
Jian, Wei Xia
Li, Hai Ling
Hou, Lei
Wei, Yi Dong
Li, Wei Ming
Xu, Ya Wei
author_facet Peng, Wen Hui
Jian, Wei Xia
Li, Hai Ling
Hou, Lei
Wei, Yi Dong
Li, Wei Ming
Xu, Ya Wei
author_sort Peng, Wen Hui
collection PubMed
description BACKGROUND: Myeloid-related protein 8/14 (MRP8/14) is a stable heterodimer formed by two different calcium-binding proteins (MRP8 and MRP14). Studies have identified that MRP8/14 regulates vascular inflammation and serves as a novel marker of acute coronary syndrome. In this study, we evaluated the correlation between serum levels of MRP8/14, hsCRP, endogenous secretory receptor for advanced glycation end-products (esRAGE) and the occurrence of coronary artery disease (CAD), or carotid intima-media thickness (IMT) when CAD was not yet developed in diabetic patients. METHODS: Serum levels of MRP8/14, esRAGE and hsCRP were measured in 375 diabetic patients. Then the results of those who had CAD were compared against who had not. Also, we investigated the associations between above-mentioned indicators and IMT of subjects without CAD in both diabetic group and non-diabetic one. RESULTS: Serum MRP8/14 was significantly higher in CAD than in non-CAD group (9.7 ± 3.6 ug/ml vs. 8.2 ± 3.0 ug/ml, P < 0.001). It was associated with severity of CAD (r = 0.16, P = 0.026). In non-CAD group, MRP8/14 was associated with IMT in patients with (r = 0.30, P < 0.001) or without diabetes (r = 0.26, P = 0.015). The areas under the curves of receiver operating characteristic for CAD were 0.63 (95% CI 0.57-0.68) for MRP8/14, 0.76 (95% CI 0.71-0.81) for hsCRP and 0.62 (95% CI 0.56 -0.67) for esRAGE. CONCLUSION: In summary, we report that diabetic patients with CAD had elevated plasma MRP8/14 levels which were also positively correlated with the severity of CAD and carotid IMT in patients without clinically overt CAD.
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spelling pubmed-31206492011-06-23 Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients Peng, Wen Hui Jian, Wei Xia Li, Hai Ling Hou, Lei Wei, Yi Dong Li, Wei Ming Xu, Ya Wei Cardiovasc Diabetol Original Investigation BACKGROUND: Myeloid-related protein 8/14 (MRP8/14) is a stable heterodimer formed by two different calcium-binding proteins (MRP8 and MRP14). Studies have identified that MRP8/14 regulates vascular inflammation and serves as a novel marker of acute coronary syndrome. In this study, we evaluated the correlation between serum levels of MRP8/14, hsCRP, endogenous secretory receptor for advanced glycation end-products (esRAGE) and the occurrence of coronary artery disease (CAD), or carotid intima-media thickness (IMT) when CAD was not yet developed in diabetic patients. METHODS: Serum levels of MRP8/14, esRAGE and hsCRP were measured in 375 diabetic patients. Then the results of those who had CAD were compared against who had not. Also, we investigated the associations between above-mentioned indicators and IMT of subjects without CAD in both diabetic group and non-diabetic one. RESULTS: Serum MRP8/14 was significantly higher in CAD than in non-CAD group (9.7 ± 3.6 ug/ml vs. 8.2 ± 3.0 ug/ml, P < 0.001). It was associated with severity of CAD (r = 0.16, P = 0.026). In non-CAD group, MRP8/14 was associated with IMT in patients with (r = 0.30, P < 0.001) or without diabetes (r = 0.26, P = 0.015). The areas under the curves of receiver operating characteristic for CAD were 0.63 (95% CI 0.57-0.68) for MRP8/14, 0.76 (95% CI 0.71-0.81) for hsCRP and 0.62 (95% CI 0.56 -0.67) for esRAGE. CONCLUSION: In summary, we report that diabetic patients with CAD had elevated plasma MRP8/14 levels which were also positively correlated with the severity of CAD and carotid IMT in patients without clinically overt CAD. BioMed Central 2011-05-18 /pmc/articles/PMC3120649/ /pubmed/21592353 http://dx.doi.org/10.1186/1475-2840-10-41 Text en Copyright ©2011 Peng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Peng, Wen Hui
Jian, Wei Xia
Li, Hai Ling
Hou, Lei
Wei, Yi Dong
Li, Wei Ming
Xu, Ya Wei
Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title_full Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title_fullStr Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title_full_unstemmed Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title_short Increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
title_sort increased serum myeloid-related protein 8/14 level is associated with atherosclerosis in type 2 diabetic patients
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120649/
https://www.ncbi.nlm.nih.gov/pubmed/21592353
http://dx.doi.org/10.1186/1475-2840-10-41
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