Cargando…

The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD

Chronic obstructive pulmonary disease (COPD) is a disease of the airways and lungs due to an enhanced inflammatory response, commonly caused by cigarette smoking. Patients with COPD are often multimorbid, as they commonly suffer from multiple chronic (inflammatory) conditions. This intensifies the b...

Descripción completa

Detalles Bibliográficos
Autores principales: Reynaert, Niki L., Vanfleteren, Lowie E. G. W., Perkins, Timothy N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219583/
https://www.ncbi.nlm.nih.gov/pubmed/37240472
http://dx.doi.org/10.3390/jcm12103366
_version_ 1785049044063617024
author Reynaert, Niki L.
Vanfleteren, Lowie E. G. W.
Perkins, Timothy N.
author_facet Reynaert, Niki L.
Vanfleteren, Lowie E. G. W.
Perkins, Timothy N.
author_sort Reynaert, Niki L.
collection PubMed
description Chronic obstructive pulmonary disease (COPD) is a disease of the airways and lungs due to an enhanced inflammatory response, commonly caused by cigarette smoking. Patients with COPD are often multimorbid, as they commonly suffer from multiple chronic (inflammatory) conditions. This intensifies the burden of individual diseases, negatively affects quality of life, and complicates disease management. COPD and comorbidities share genetic and lifestyle-related risk factors and pathobiological mechanisms, including chronic inflammation and oxidative stress. The receptor for advanced glycation end products (RAGE) is an important driver of chronic inflammation. Advanced glycation end products (AGEs) are RAGE ligands that accumulate due to aging, inflammation, oxidative stress, and carbohydrate metabolism. AGEs cause further inflammation and oxidative stress through RAGE, but also through RAGE-independent mechanisms. This review describes the complexity of RAGE signaling and the causes of AGE accumulation, followed by a comprehensive overview of alterations reported on AGEs and RAGE in COPD and in important co-morbidities. Furthermore, it describes the mechanisms by which AGEs and RAGE contribute to the pathophysiology of individual disease conditions and how they execute crosstalk between organ systems. A section on therapeutic strategies that target AGEs and RAGE and could alleviate patients from multimorbid conditions using single therapeutics concludes this review.
format Online
Article
Text
id pubmed-10219583
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-102195832023-05-27 The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD Reynaert, Niki L. Vanfleteren, Lowie E. G. W. Perkins, Timothy N. J Clin Med Review Chronic obstructive pulmonary disease (COPD) is a disease of the airways and lungs due to an enhanced inflammatory response, commonly caused by cigarette smoking. Patients with COPD are often multimorbid, as they commonly suffer from multiple chronic (inflammatory) conditions. This intensifies the burden of individual diseases, negatively affects quality of life, and complicates disease management. COPD and comorbidities share genetic and lifestyle-related risk factors and pathobiological mechanisms, including chronic inflammation and oxidative stress. The receptor for advanced glycation end products (RAGE) is an important driver of chronic inflammation. Advanced glycation end products (AGEs) are RAGE ligands that accumulate due to aging, inflammation, oxidative stress, and carbohydrate metabolism. AGEs cause further inflammation and oxidative stress through RAGE, but also through RAGE-independent mechanisms. This review describes the complexity of RAGE signaling and the causes of AGE accumulation, followed by a comprehensive overview of alterations reported on AGEs and RAGE in COPD and in important co-morbidities. Furthermore, it describes the mechanisms by which AGEs and RAGE contribute to the pathophysiology of individual disease conditions and how they execute crosstalk between organ systems. A section on therapeutic strategies that target AGEs and RAGE and could alleviate patients from multimorbid conditions using single therapeutics concludes this review. MDPI 2023-05-09 /pmc/articles/PMC10219583/ /pubmed/37240472 http://dx.doi.org/10.3390/jcm12103366 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 Review
Reynaert, Niki L.
Vanfleteren, Lowie E. G. W.
Perkins, Timothy N.
The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title_full The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title_fullStr The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title_full_unstemmed The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title_short The AGE-RAGE Axis and the Pathophysiology of Multimorbidity in COPD
title_sort age-rage axis and the pathophysiology of multimorbidity in copd
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219583/
https://www.ncbi.nlm.nih.gov/pubmed/37240472
http://dx.doi.org/10.3390/jcm12103366
work_keys_str_mv AT reynaertnikil theagerageaxisandthepathophysiologyofmultimorbidityincopd
AT vanfleterenlowieegw theagerageaxisandthepathophysiologyofmultimorbidityincopd
AT perkinstimothyn theagerageaxisandthepathophysiologyofmultimorbidityincopd
AT reynaertnikil agerageaxisandthepathophysiologyofmultimorbidityincopd
AT vanfleterenlowieegw agerageaxisandthepathophysiologyofmultimorbidityincopd
AT perkinstimothyn agerageaxisandthepathophysiologyofmultimorbidityincopd