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Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients

The formation of advanced glycation end products (AGEs), in various tissues has been known to enhance immunoinflammatory reactions and local oxidant stresses in long standing diabetes. Recently, AGEs have been reported to play a role in neointimal formation in animal models of arterial injury. We at...

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Autores principales: Choi, Eui-Young, Kwon, Hyuck Moon, Ahn, Chul-Woo, Lee, Geun Taek, Joung, Boyoung, Hong, Bum Kee, Yoon, Young Won, Kim, Dongsoo, Byun, Ki-Hyun, Kang, Tae Soo, Yoon, Se-Jung, Kwon, Sung Woo, Lee, Sung-Ju, Park, Jong-Kwan, Kim, Hyun-Seung
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823061/
https://www.ncbi.nlm.nih.gov/pubmed/15744809
http://dx.doi.org/10.3349/ymj.2005.46.1.78
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author Choi, Eui-Young
Kwon, Hyuck Moon
Ahn, Chul-Woo
Lee, Geun Taek
Joung, Boyoung
Hong, Bum Kee
Yoon, Young Won
Kim, Dongsoo
Byun, Ki-Hyun
Kang, Tae Soo
Yoon, Se-Jung
Kwon, Sung Woo
Lee, Sung-Ju
Park, Jong-Kwan
Kim, Hyun-Seung
author_facet Choi, Eui-Young
Kwon, Hyuck Moon
Ahn, Chul-Woo
Lee, Geun Taek
Joung, Boyoung
Hong, Bum Kee
Yoon, Young Won
Kim, Dongsoo
Byun, Ki-Hyun
Kang, Tae Soo
Yoon, Se-Jung
Kwon, Sung Woo
Lee, Sung-Ju
Park, Jong-Kwan
Kim, Hyun-Seung
author_sort Choi, Eui-Young
collection PubMed
description The formation of advanced glycation end products (AGEs), in various tissues has been known to enhance immunoinflammatory reactions and local oxidant stresses in long standing diabetes. Recently, AGEs have been reported to play a role in neointimal formation in animal models of arterial injury. We attempted to determine whether the serum levels of AGEs are associated with coronary restenosis in diabetic patients. Blood samples were collected from diabetic patients with coronary artery disease undergoing stent implantation and the serum levels of AGEs were analyzed by the fluorescent intensity method. The development of in-stent restenosis (ISR) was evaluated by a 6-month follow-up coronary angiography. A total of 263 target lesions were evaluated, in 203 patients. The ISR rate in the high-AGE (>170 U/ml) group (40.1%) was significantly higher than in the low-AGE group (≤170 U/ml) (19.6%) (p<0.001). Furthermore, multivariate analysis revealed that a high level of serum AGEs is an independent risk factor for the development of ISR (odds ratio, 2.659; 95% CI, 1.431-4.940; p=0.002). The serum levels of AGEs constitute an excellent predictive factor for ISR, and should be one of the guidelines for medical therapy and interventional strategy to prevent ISR in diabetic patients.
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spelling pubmed-28230612010-02-17 Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients Choi, Eui-Young Kwon, Hyuck Moon Ahn, Chul-Woo Lee, Geun Taek Joung, Boyoung Hong, Bum Kee Yoon, Young Won Kim, Dongsoo Byun, Ki-Hyun Kang, Tae Soo Yoon, Se-Jung Kwon, Sung Woo Lee, Sung-Ju Park, Jong-Kwan Kim, Hyun-Seung Yonsei Med J Original Article The formation of advanced glycation end products (AGEs), in various tissues has been known to enhance immunoinflammatory reactions and local oxidant stresses in long standing diabetes. Recently, AGEs have been reported to play a role in neointimal formation in animal models of arterial injury. We attempted to determine whether the serum levels of AGEs are associated with coronary restenosis in diabetic patients. Blood samples were collected from diabetic patients with coronary artery disease undergoing stent implantation and the serum levels of AGEs were analyzed by the fluorescent intensity method. The development of in-stent restenosis (ISR) was evaluated by a 6-month follow-up coronary angiography. A total of 263 target lesions were evaluated, in 203 patients. The ISR rate in the high-AGE (>170 U/ml) group (40.1%) was significantly higher than in the low-AGE group (≤170 U/ml) (19.6%) (p<0.001). Furthermore, multivariate analysis revealed that a high level of serum AGEs is an independent risk factor for the development of ISR (odds ratio, 2.659; 95% CI, 1.431-4.940; p=0.002). The serum levels of AGEs constitute an excellent predictive factor for ISR, and should be one of the guidelines for medical therapy and interventional strategy to prevent ISR in diabetic patients. Yonsei University College of Medicine 2005-02-28 2005-02-28 /pmc/articles/PMC2823061/ /pubmed/15744809 http://dx.doi.org/10.3349/ymj.2005.46.1.78 Text en Copyright © 2005 The Yonsei University College of Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Eui-Young
Kwon, Hyuck Moon
Ahn, Chul-Woo
Lee, Geun Taek
Joung, Boyoung
Hong, Bum Kee
Yoon, Young Won
Kim, Dongsoo
Byun, Ki-Hyun
Kang, Tae Soo
Yoon, Se-Jung
Kwon, Sung Woo
Lee, Sung-Ju
Park, Jong-Kwan
Kim, Hyun-Seung
Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title_full Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title_fullStr Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title_full_unstemmed Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title_short Serum Levels of Advanced Glycation End Products Are Associated with In-Stent Restenosis in Diabetic Patients
title_sort serum levels of advanced glycation end products are associated with in-stent restenosis in diabetic patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823061/
https://www.ncbi.nlm.nih.gov/pubmed/15744809
http://dx.doi.org/10.3349/ymj.2005.46.1.78
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