Cargando…

The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification

As a person ages, mitral annular calcification develops in the mitral annulus with increasing frequency. Lipid deposition, inflammation, and aging-related degeneration have been cited as potential causes of this pathophysiology, though there is currently no conclusive evidence to support this. AGEs...

Descripción completa

Detalles Bibliográficos
Autores principales: Boyraz, Bedrettin, Peker, Tezcan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531500/
https://www.ncbi.nlm.nih.gov/pubmed/37754835
http://dx.doi.org/10.3390/jcdd10090406
_version_ 1785111733455552512
author Boyraz, Bedrettin
Peker, Tezcan
author_facet Boyraz, Bedrettin
Peker, Tezcan
author_sort Boyraz, Bedrettin
collection PubMed
description As a person ages, mitral annular calcification develops in the mitral annulus with increasing frequency. Lipid deposition, inflammation, and aging-related degeneration have been cited as potential causes of this pathophysiology, though there is currently no conclusive evidence to support this. AGEs accumulate in tissues due to the glycation of proteins and lipids, increasing the release of proinflammatory cytokines secondary to oxidative stress through the AGE receptor. The AGE levels increase in diabetic microvascular complications and degenerative aortic valve disease. Our study was planned prospectively as a case–control study involving 94 MAC-positive patients and 94 MAC-negative patients. The demographics, echocardiographic data and AGE levels of the patients were measured and recorded using the skin autofluorescence method. AGE levels were significantly higher in the MAC-positive patient group (3.2 vs. 2.7; p < 0.001). The AGE levels were observed as an independent predictor of MAC development in a regression analysis (OR: 8.05, 95% CI: 3.74–17.33, p < 0.001). In a ROC-curve analysis, the AUC was 0.79 (95% CI: 0.72–0.85). At a cut-off value of 2.7, 79.7% sensitivity and 69.1% specificity were observed. AGE levels can be used to cheaply, easily and non-invasively identify patients at risk of developing MAC.
format Online
Article
Text
id pubmed-10531500
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-105315002023-09-28 The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification Boyraz, Bedrettin Peker, Tezcan J Cardiovasc Dev Dis Article As a person ages, mitral annular calcification develops in the mitral annulus with increasing frequency. Lipid deposition, inflammation, and aging-related degeneration have been cited as potential causes of this pathophysiology, though there is currently no conclusive evidence to support this. AGEs accumulate in tissues due to the glycation of proteins and lipids, increasing the release of proinflammatory cytokines secondary to oxidative stress through the AGE receptor. The AGE levels increase in diabetic microvascular complications and degenerative aortic valve disease. Our study was planned prospectively as a case–control study involving 94 MAC-positive patients and 94 MAC-negative patients. The demographics, echocardiographic data and AGE levels of the patients were measured and recorded using the skin autofluorescence method. AGE levels were significantly higher in the MAC-positive patient group (3.2 vs. 2.7; p < 0.001). The AGE levels were observed as an independent predictor of MAC development in a regression analysis (OR: 8.05, 95% CI: 3.74–17.33, p < 0.001). In a ROC-curve analysis, the AUC was 0.79 (95% CI: 0.72–0.85). At a cut-off value of 2.7, 79.7% sensitivity and 69.1% specificity were observed. AGE levels can be used to cheaply, easily and non-invasively identify patients at risk of developing MAC. MDPI 2023-09-20 /pmc/articles/PMC10531500/ /pubmed/37754835 http://dx.doi.org/10.3390/jcdd10090406 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Boyraz, Bedrettin
Peker, Tezcan
The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title_full The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title_fullStr The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title_full_unstemmed The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title_short The Role of Advanced Glycation End-Product Levels Measured by Skin Autofluorescence in the Development of Mitral Annular Calcification
title_sort role of advanced glycation end-product levels measured by skin autofluorescence in the development of mitral annular calcification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531500/
https://www.ncbi.nlm.nih.gov/pubmed/37754835
http://dx.doi.org/10.3390/jcdd10090406
work_keys_str_mv AT boyrazbedrettin theroleofadvancedglycationendproductlevelsmeasuredbyskinautofluorescenceinthedevelopmentofmitralannularcalcification
AT pekertezcan theroleofadvancedglycationendproductlevelsmeasuredbyskinautofluorescenceinthedevelopmentofmitralannularcalcification
AT boyrazbedrettin roleofadvancedglycationendproductlevelsmeasuredbyskinautofluorescenceinthedevelopmentofmitralannularcalcification
AT pekertezcan roleofadvancedglycationendproductlevelsmeasuredbyskinautofluorescenceinthedevelopmentofmitralannularcalcification