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Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes
Critical Limb Ischemia (CLI) is common but uncommonly diagnosed. Improved recognition and early diagnostic markers for CLI are needed. Therefore, the aim of our study was to identify plasma biomarkers of CLI in patients with type 2 diabetes mellitus (T2DM). In this study, antibody-coated glass slide...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595823/ https://www.ncbi.nlm.nih.gov/pubmed/28900239 http://dx.doi.org/10.1038/s41598-017-11820-x |
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author | Li, Ju-yi Yang, Xiao-yan Wang, Xiu-fang Jia, Xiong Wang, Zhong-jing Deng, Ai-ping Bai, Xiang-li Zhu, Lin Li, Bing-hui Feng, Zi-bo Li, Ye Wang, Ling Jin, Si |
author_facet | Li, Ju-yi Yang, Xiao-yan Wang, Xiu-fang Jia, Xiong Wang, Zhong-jing Deng, Ai-ping Bai, Xiang-li Zhu, Lin Li, Bing-hui Feng, Zi-bo Li, Ye Wang, Ling Jin, Si |
author_sort | Li, Ju-yi |
collection | PubMed |
description | Critical Limb Ischemia (CLI) is common but uncommonly diagnosed. Improved recognition and early diagnostic markers for CLI are needed. Therefore, the aim of our study was to identify plasma biomarkers of CLI in patients with type 2 diabetes mellitus (T2DM). In this study, antibody-coated glass slide arrays were used to determine the plasma levels of 274 human cytokines in four matched cases of diabetes with and without CLI. Potential biomarkers were confirmed in an independent cohort by ELISA. After adjusting for confounding risk factors, only plasma level of Siglec-5 remained significantly associated with an increased odds ratio (OR) for diabetes with CLI by binary logistic regression analysis. Receiver operating characteristic (ROC) curve analysis revealed the optimal cut-off points for Siglec-5 was 153.1 ng/ml. After entering Siglec-5, the AUC was 0.99, which was higher than that of confounding risk factors only (AUC = 0.97, P < 0.05). Siglec-5 was expressed in plaques, but not in healthy artery wall in T2DM patients. Elevated plasma Siglec-5 was independently associated with CLI in T2DM. Plasma Siglec-5 levels are implicated as an early diagnostic marker of CLI in T2DM patients and it may become a target for the prevention or treatment of CLI in diabetes. |
format | Online Article Text |
id | pubmed-5595823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55958232017-09-14 Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes Li, Ju-yi Yang, Xiao-yan Wang, Xiu-fang Jia, Xiong Wang, Zhong-jing Deng, Ai-ping Bai, Xiang-li Zhu, Lin Li, Bing-hui Feng, Zi-bo Li, Ye Wang, Ling Jin, Si Sci Rep Article Critical Limb Ischemia (CLI) is common but uncommonly diagnosed. Improved recognition and early diagnostic markers for CLI are needed. Therefore, the aim of our study was to identify plasma biomarkers of CLI in patients with type 2 diabetes mellitus (T2DM). In this study, antibody-coated glass slide arrays were used to determine the plasma levels of 274 human cytokines in four matched cases of diabetes with and without CLI. Potential biomarkers were confirmed in an independent cohort by ELISA. After adjusting for confounding risk factors, only plasma level of Siglec-5 remained significantly associated with an increased odds ratio (OR) for diabetes with CLI by binary logistic regression analysis. Receiver operating characteristic (ROC) curve analysis revealed the optimal cut-off points for Siglec-5 was 153.1 ng/ml. After entering Siglec-5, the AUC was 0.99, which was higher than that of confounding risk factors only (AUC = 0.97, P < 0.05). Siglec-5 was expressed in plaques, but not in healthy artery wall in T2DM patients. Elevated plasma Siglec-5 was independently associated with CLI in T2DM. Plasma Siglec-5 levels are implicated as an early diagnostic marker of CLI in T2DM patients and it may become a target for the prevention or treatment of CLI in diabetes. Nature Publishing Group UK 2017-09-12 /pmc/articles/PMC5595823/ /pubmed/28900239 http://dx.doi.org/10.1038/s41598-017-11820-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Ju-yi Yang, Xiao-yan Wang, Xiu-fang Jia, Xiong Wang, Zhong-jing Deng, Ai-ping Bai, Xiang-li Zhu, Lin Li, Bing-hui Feng, Zi-bo Li, Ye Wang, Ling Jin, Si Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title | Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title_full | Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title_fullStr | Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title_full_unstemmed | Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title_short | Siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
title_sort | siglec-5 is a novel marker of critical limb ischemia in patients with diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595823/ https://www.ncbi.nlm.nih.gov/pubmed/28900239 http://dx.doi.org/10.1038/s41598-017-11820-x |
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