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.

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. - In: JOURNAL OF INTERNATIONAL MEDICAL RESEARCH. - ISSN 0300-0605. - 44:1_suppl(2016), pp. 76-80. [10.1177/0300060515593255]

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

Erre, Gian Luca;TARAS, Loredana;SABA, PIER SERGIO;GANAU, Antonello;CARRU, Ciriaco;PASSIU, Giuseppe
2016-01-01

Abstract

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.
2016
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. - In: JOURNAL OF INTERNATIONAL MEDICAL RESEARCH. - ISSN 0300-0605. - 44:1_suppl(2016), pp. 76-80. [10.1177/0300060515593255]
File in questo prodotto:
File Dimensione Formato  
0300060515593255.pdf

accesso aperto

Tipologia: Versione editoriale (versione finale pubblicata)
Licenza: Creative commons
Dimensione 135.39 kB
Formato Adobe PDF
135.39 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/174605
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 23
  • ???jsp.display-item.citation.isi??? 22
social impact