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Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis
Rheumatoid arthritis (RA) is a chronic, systemic, inflammatory autoimmune disease that affects about 1% of the global population, with a female–male ratio of 3:1. RA preferably affects the joints, with consequent joint swelling and deformities followed by ankylosis. However, evidence has accumulated...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827097/ https://www.ncbi.nlm.nih.gov/pubmed/33435178 http://dx.doi.org/10.3390/biom11010081 |
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author | Maiuolo, Jessica Muscoli, Carolina Gliozzi, Micaela Musolino, Vincenzo Carresi, Cristina Paone, Sara Ilari, Sara Mollace, Rocco Palma, Ernesto Mollace, Vincenzo |
author_facet | Maiuolo, Jessica Muscoli, Carolina Gliozzi, Micaela Musolino, Vincenzo Carresi, Cristina Paone, Sara Ilari, Sara Mollace, Rocco Palma, Ernesto Mollace, Vincenzo |
author_sort | Maiuolo, Jessica |
collection | PubMed |
description | Rheumatoid arthritis (RA) is a chronic, systemic, inflammatory autoimmune disease that affects about 1% of the global population, with a female–male ratio of 3:1. RA preferably affects the joints, with consequent joint swelling and deformities followed by ankylosis. However, evidence has accumulated showing that patients suffering from RA can also develop extra-articular manifestations, including cardiovascular disease states, neuropathies, and multiorgan dysfunction. In particular, peripheral nerve disorders showed a consistent impact in the course of the disease (prevalence about 20%) mostly associated to vasculitis of the nerve vessels leading to vascular ischemia, axonal degeneration, and neuronal demyelination. The pathophysiological basis of this RA-associated microvascular disease, which leads to impairment of assonal functionality, is still to be better clarified. However, endothelial dysfunction and alterations of the so-called brain-nerve barrier (BNB) seem to play a fundamental role. This review aims to assess the potential mechanisms underlying the impairment of endothelial cell functionality in the development of RA and to identify the role of dysfunctional endothelium as a causative mechanism of extra-articular manifestation of RA. On the other hand, the potential impact of lifestyle and nutritional interventions targeting the maintenance of endothelial cell integrity in patients with RA will be discussed as a potential option when approaching therapeutic solutions in the course of the disease. |
format | Online Article Text |
id | pubmed-7827097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78270972021-01-25 Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis Maiuolo, Jessica Muscoli, Carolina Gliozzi, Micaela Musolino, Vincenzo Carresi, Cristina Paone, Sara Ilari, Sara Mollace, Rocco Palma, Ernesto Mollace, Vincenzo Biomolecules Review Rheumatoid arthritis (RA) is a chronic, systemic, inflammatory autoimmune disease that affects about 1% of the global population, with a female–male ratio of 3:1. RA preferably affects the joints, with consequent joint swelling and deformities followed by ankylosis. However, evidence has accumulated showing that patients suffering from RA can also develop extra-articular manifestations, including cardiovascular disease states, neuropathies, and multiorgan dysfunction. In particular, peripheral nerve disorders showed a consistent impact in the course of the disease (prevalence about 20%) mostly associated to vasculitis of the nerve vessels leading to vascular ischemia, axonal degeneration, and neuronal demyelination. The pathophysiological basis of this RA-associated microvascular disease, which leads to impairment of assonal functionality, is still to be better clarified. However, endothelial dysfunction and alterations of the so-called brain-nerve barrier (BNB) seem to play a fundamental role. This review aims to assess the potential mechanisms underlying the impairment of endothelial cell functionality in the development of RA and to identify the role of dysfunctional endothelium as a causative mechanism of extra-articular manifestation of RA. On the other hand, the potential impact of lifestyle and nutritional interventions targeting the maintenance of endothelial cell integrity in patients with RA will be discussed as a potential option when approaching therapeutic solutions in the course of the disease. MDPI 2021-01-10 /pmc/articles/PMC7827097/ /pubmed/33435178 http://dx.doi.org/10.3390/biom11010081 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Maiuolo, Jessica Muscoli, Carolina Gliozzi, Micaela Musolino, Vincenzo Carresi, Cristina Paone, Sara Ilari, Sara Mollace, Rocco Palma, Ernesto Mollace, Vincenzo Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title | Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title_full | Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title_fullStr | Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title_full_unstemmed | Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title_short | Endothelial Dysfunction and Extra-Articular Neurological Manifestations in Rheumatoid Arthritis |
title_sort | endothelial dysfunction and extra-articular neurological manifestations in rheumatoid arthritis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827097/ https://www.ncbi.nlm.nih.gov/pubmed/33435178 http://dx.doi.org/10.3390/biom11010081 |
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