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Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study

OBJECTIVE: To investigate whether levels of asymmetric dimethylarginine (ADMA), as a measure of endothelial dysfunction, are higher in patients with rheumatoid arthritis compared with healthy control subjects. The relationships between ADMA and surrogate measures of arterial stiffness were evaluated...

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Autores principales: Erre, Gian Luca, Piras, Alessandra, Mura, Silvia, Mundula, Nicola, Piras, Marco, Taras, Loredana, Longu, Maria Giovanna, Saba, Pier Sergio, Ganau, Antonello, Carru, Ciriaco, Passiu, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536534/
https://www.ncbi.nlm.nih.gov/pubmed/27683145
http://dx.doi.org/10.1177/0300060515593255
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author Erre, Gian Luca
Piras, Alessandra
Mura, Silvia
Mundula, Nicola
Piras, Marco
Taras, Loredana
Longu, Maria Giovanna
Saba, Pier Sergio
Ganau, Antonello
Carru, Ciriaco
Passiu, Giuseppe
author_facet Erre, Gian Luca
Piras, Alessandra
Mura, Silvia
Mundula, Nicola
Piras, Marco
Taras, Loredana
Longu, Maria Giovanna
Saba, Pier Sergio
Ganau, Antonello
Carru, Ciriaco
Passiu, Giuseppe
author_sort Erre, Gian Luca
collection PubMed
description OBJECTIVE: To investigate whether levels of asymmetric dimethylarginine (ADMA), as a measure of endothelial dysfunction, are higher in patients with rheumatoid arthritis compared with healthy control subjects. The relationships between ADMA and surrogate measures of arterial stiffness were evaluated. METHODS: Patients with rheumatoid arthritis and healthy control subjects were recruited. ADMA was quantified via enzyme-linked immunosorbent assay. Arterial stiffness was evaluated using pulse wave analysis. RESULTS: There was no significant difference in plasma ADMA concentration between patients with rheumatoid arthritis (n = 30) and healthy controls (n = 30). Aortic augmentation pressure was significantly higher in patients than in controls. C-reactive protein and Health Assessment Questionnaire score were independent predictors of arterial stiffness in patients. There was no relationship between ADMA concentration and aortic augmentation pressure in the study population as a whole. CONCLUSIONS: Arterial stiffness appears to be increased in rheumatoid arthritis and independently associated with systemic inflammation and physical disability. ADMA concentration was not increased in this small group of patients with rheumatoid arthritis compared with healthy controls; nor was it associated with arterial stiffness.
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spelling pubmed-55365342017-10-03 Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study Erre, Gian Luca Piras, Alessandra Mura, Silvia Mundula, Nicola Piras, Marco Taras, Loredana Longu, Maria Giovanna Saba, Pier Sergio Ganau, Antonello Carru, Ciriaco Passiu, Giuseppe J Int Med Res Immuno-Mediated Diseases and CV Risk OBJECTIVE: To investigate whether levels of asymmetric dimethylarginine (ADMA), as a measure of endothelial dysfunction, are higher in patients with rheumatoid arthritis compared with healthy control subjects. The relationships between ADMA and surrogate measures of arterial stiffness were evaluated. METHODS: Patients with rheumatoid arthritis and healthy control subjects were recruited. ADMA was quantified via enzyme-linked immunosorbent assay. Arterial stiffness was evaluated using pulse wave analysis. RESULTS: There was no significant difference in plasma ADMA concentration between patients with rheumatoid arthritis (n = 30) and healthy controls (n = 30). Aortic augmentation pressure was significantly higher in patients than in controls. C-reactive protein and Health Assessment Questionnaire score were independent predictors of arterial stiffness in patients. There was no relationship between ADMA concentration and aortic augmentation pressure in the study population as a whole. CONCLUSIONS: Arterial stiffness appears to be increased in rheumatoid arthritis and independently associated with systemic inflammation and physical disability. ADMA concentration was not increased in this small group of patients with rheumatoid arthritis compared with healthy controls; nor was it associated with arterial stiffness. SAGE Publications 2016-09-28 2016-09 /pmc/articles/PMC5536534/ /pubmed/27683145 http://dx.doi.org/10.1177/0300060515593255 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Immuno-Mediated Diseases and CV Risk
Erre, Gian Luca
Piras, Alessandra
Mura, Silvia
Mundula, Nicola
Piras, Marco
Taras, Loredana
Longu, Maria Giovanna
Saba, Pier Sergio
Ganau, Antonello
Carru, Ciriaco
Passiu, Giuseppe
Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title_full Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title_fullStr Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title_full_unstemmed Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title_short Asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: A case–control study
title_sort asymmetric dimethylarginine and arterial stiffness in patients with rheumatoid arthritis: a case–control study
topic Immuno-Mediated Diseases and CV Risk
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536534/
https://www.ncbi.nlm.nih.gov/pubmed/27683145
http://dx.doi.org/10.1177/0300060515593255
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