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Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus

BACKGROUND: Soluble C-X-C chemokine ligand 16 (CXCL16), a scavenger receptor for oxidized low density lipoprotein, has been shown to promote atherogenic effects in vivo and to predict long-term mortality in acute coronary syndrome. The aim of this study was to explore the association of circulating...

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Autores principales: Zhao, Leping, Wu, Fan, Jin, Leigang, Lu, Tingting, Yang, Lihui, Pan, Xuebo, Shao, Chuanfeng, Li, Xiaokun, Lin, Zhuofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906379/
https://www.ncbi.nlm.nih.gov/pubmed/24489966
http://dx.doi.org/10.1371/journal.pone.0087786
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author Zhao, Leping
Wu, Fan
Jin, Leigang
Lu, Tingting
Yang, Lihui
Pan, Xuebo
Shao, Chuanfeng
Li, Xiaokun
Lin, Zhuofeng
author_facet Zhao, Leping
Wu, Fan
Jin, Leigang
Lu, Tingting
Yang, Lihui
Pan, Xuebo
Shao, Chuanfeng
Li, Xiaokun
Lin, Zhuofeng
author_sort Zhao, Leping
collection PubMed
description BACKGROUND: Soluble C-X-C chemokine ligand 16 (CXCL16), a scavenger receptor for oxidized low density lipoprotein, has been shown to promote atherogenic effects in vivo and to predict long-term mortality in acute coronary syndrome. The aim of this study was to explore the association of circulating CXCL16 levels with diabetic subjects with and without renal disease. METHODOLOGY/PRINCIPAL FINDINGS: One hundred twenty Chinese subjects, which included patients with type 2 diabetes mellitus (T2DM), diabetic nephropathy (DN), and CKD, as well as healthy controls, were enrolled in this study. Serum CXCL16 levels were examined by immunoassay and other clinical biochemical parameters were tested based on standard methods. Our results indicated that, HDL and LDL cholesterol levels are significantly different in DN but not in T2D patients in comparison with healthy subjects. On the other hand, Serum CXCL16 levels were significantly increased in DN subjects compared with age and gender matched healthy and T2DM subjects (p<0.05 respectively). However, no significant changes in serum CXCL16 levels were found between T2DM and healthy subjects. Furthermore, serum CXCL16 concentration negatively correlated with estimated glomerular filtrate rate, creatinine clearance rate and blood albumin, and positively with 24 h proteinuria, blood urea nitrogen (BUN), creatinine, and uric acid after adjusting for age, gender and BMI in subjects with DN. Multiple stepwise regression analyses indicated that serum CXCL16 levels were independently associated with serum 24 h proteinuria, and BUN (p<0.05 respectively). CONCLUSION: Serum CXCL16 may be an indicator of renal injury in subjects with T2DM. Understanding the exact mechanism of elevated CXCL16 in subjects with DN requires further study.
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spelling pubmed-39063792014-01-31 Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus Zhao, Leping Wu, Fan Jin, Leigang Lu, Tingting Yang, Lihui Pan, Xuebo Shao, Chuanfeng Li, Xiaokun Lin, Zhuofeng PLoS One Research Article BACKGROUND: Soluble C-X-C chemokine ligand 16 (CXCL16), a scavenger receptor for oxidized low density lipoprotein, has been shown to promote atherogenic effects in vivo and to predict long-term mortality in acute coronary syndrome. The aim of this study was to explore the association of circulating CXCL16 levels with diabetic subjects with and without renal disease. METHODOLOGY/PRINCIPAL FINDINGS: One hundred twenty Chinese subjects, which included patients with type 2 diabetes mellitus (T2DM), diabetic nephropathy (DN), and CKD, as well as healthy controls, were enrolled in this study. Serum CXCL16 levels were examined by immunoassay and other clinical biochemical parameters were tested based on standard methods. Our results indicated that, HDL and LDL cholesterol levels are significantly different in DN but not in T2D patients in comparison with healthy subjects. On the other hand, Serum CXCL16 levels were significantly increased in DN subjects compared with age and gender matched healthy and T2DM subjects (p<0.05 respectively). However, no significant changes in serum CXCL16 levels were found between T2DM and healthy subjects. Furthermore, serum CXCL16 concentration negatively correlated with estimated glomerular filtrate rate, creatinine clearance rate and blood albumin, and positively with 24 h proteinuria, blood urea nitrogen (BUN), creatinine, and uric acid after adjusting for age, gender and BMI in subjects with DN. Multiple stepwise regression analyses indicated that serum CXCL16 levels were independently associated with serum 24 h proteinuria, and BUN (p<0.05 respectively). CONCLUSION: Serum CXCL16 may be an indicator of renal injury in subjects with T2DM. Understanding the exact mechanism of elevated CXCL16 in subjects with DN requires further study. Public Library of Science 2014-01-29 /pmc/articles/PMC3906379/ /pubmed/24489966 http://dx.doi.org/10.1371/journal.pone.0087786 Text en © 2014 Zhao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhao, Leping
Wu, Fan
Jin, Leigang
Lu, Tingting
Yang, Lihui
Pan, Xuebo
Shao, Chuanfeng
Li, Xiaokun
Lin, Zhuofeng
Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title_full Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title_fullStr Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title_full_unstemmed Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title_short Serum CXCL16 as a Novel Marker of Renal Injury in Type 2 Diabetes Mellitus
title_sort serum cxcl16 as a novel marker of renal injury in type 2 diabetes mellitus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906379/
https://www.ncbi.nlm.nih.gov/pubmed/24489966
http://dx.doi.org/10.1371/journal.pone.0087786
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