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Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?

Prosthetic joint infection (PJI) is the most common cause of failure of total joint arthroplasty, but a gold standard for PJI diagnosis is still lacking. Advanced glycation end products (AGEs) are proinflammatory molecules inducing intracellular oxidative stress (OS) after binding to their cell memb...

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Autores principales: Massaccesi, Luca, Bonomelli, Barbara, Marazzi, Monica Gioia, Drago, Lorenzo, Romanelli, Massimiliano Marco Corsi, Erba, Daniela, Papini, Nadia, Barassi, Alessandra, Goi, Giancarlo, Galliera, Emanuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745725/
https://www.ncbi.nlm.nih.gov/pubmed/29386700
http://dx.doi.org/10.1155/2017/6140896
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author Massaccesi, Luca
Bonomelli, Barbara
Marazzi, Monica Gioia
Drago, Lorenzo
Romanelli, Massimiliano Marco Corsi
Erba, Daniela
Papini, Nadia
Barassi, Alessandra
Goi, Giancarlo
Galliera, Emanuela
author_facet Massaccesi, Luca
Bonomelli, Barbara
Marazzi, Monica Gioia
Drago, Lorenzo
Romanelli, Massimiliano Marco Corsi
Erba, Daniela
Papini, Nadia
Barassi, Alessandra
Goi, Giancarlo
Galliera, Emanuela
author_sort Massaccesi, Luca
collection PubMed
description Prosthetic joint infection (PJI) is the most common cause of failure of total joint arthroplasty, but a gold standard for PJI diagnosis is still lacking. Advanced glycation end products (AGEs) are proinflammatory molecules inducing intracellular oxidative stress (OS) after binding to their cell membrane receptors (RAGE). The aim of this study was to evaluate plasmatic soluble receptor for advanced glycation end products (sRAGE), as a new OS and infection marker correlating sRAGE to the level of OS and antioxidant defenses, in PJI, in order to explore the possible application of this new biomarker in the early diagnosis of PJI. Plasmatic sRAGE levels (by ELISA assay), plasma antioxidant total defenses (by lag time method), plasma reactive oxygen species (ROS), and thiobarbituric acid reactive substance (TBARS) levels (by colorimetric assay) were evaluated in 11 PJI patients and in 30 matched controls. ROS and TBARS were significantly higher (p < 0.001) while plasma total antioxidant capacity and sRAGE were significantly lower (p < 0.01) in patients with PJI compared to controls. Our results confirm the OS in PJI and show a strong negative correlation between the level of sRAGE and oxidative status, suggesting the plasmatic sRAGE as a potential marker for improving PJI early diagnosis.
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spelling pubmed-57457252018-01-31 Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections? Massaccesi, Luca Bonomelli, Barbara Marazzi, Monica Gioia Drago, Lorenzo Romanelli, Massimiliano Marco Corsi Erba, Daniela Papini, Nadia Barassi, Alessandra Goi, Giancarlo Galliera, Emanuela Dis Markers Research Article Prosthetic joint infection (PJI) is the most common cause of failure of total joint arthroplasty, but a gold standard for PJI diagnosis is still lacking. Advanced glycation end products (AGEs) are proinflammatory molecules inducing intracellular oxidative stress (OS) after binding to their cell membrane receptors (RAGE). The aim of this study was to evaluate plasmatic soluble receptor for advanced glycation end products (sRAGE), as a new OS and infection marker correlating sRAGE to the level of OS and antioxidant defenses, in PJI, in order to explore the possible application of this new biomarker in the early diagnosis of PJI. Plasmatic sRAGE levels (by ELISA assay), plasma antioxidant total defenses (by lag time method), plasma reactive oxygen species (ROS), and thiobarbituric acid reactive substance (TBARS) levels (by colorimetric assay) were evaluated in 11 PJI patients and in 30 matched controls. ROS and TBARS were significantly higher (p < 0.001) while plasma total antioxidant capacity and sRAGE were significantly lower (p < 0.01) in patients with PJI compared to controls. Our results confirm the OS in PJI and show a strong negative correlation between the level of sRAGE and oxidative status, suggesting the plasmatic sRAGE as a potential marker for improving PJI early diagnosis. Hindawi 2017 2017-12-13 /pmc/articles/PMC5745725/ /pubmed/29386700 http://dx.doi.org/10.1155/2017/6140896 Text en Copyright © 2017 Luca Massaccesi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Massaccesi, Luca
Bonomelli, Barbara
Marazzi, Monica Gioia
Drago, Lorenzo
Romanelli, Massimiliano Marco Corsi
Erba, Daniela
Papini, Nadia
Barassi, Alessandra
Goi, Giancarlo
Galliera, Emanuela
Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title_full Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title_fullStr Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title_full_unstemmed Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title_short Plasmatic Soluble Receptor for Advanced Glycation End Products as a New Oxidative Stress Biomarker in Patients with Prosthetic-Joint-Associated Infections?
title_sort plasmatic soluble receptor for advanced glycation end products as a new oxidative stress biomarker in patients with prosthetic-joint-associated infections?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745725/
https://www.ncbi.nlm.nih.gov/pubmed/29386700
http://dx.doi.org/10.1155/2017/6140896
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