Adalimumab decreases aortic stiffness independently of its effect in disease activity in patients with rheumatoid arthritis

Rheumatoid arthritis (RA) is associated with increased cardiovascular morbidity and mortality attributed to traditional cardiovascular risk factors and/or the chronic systemic inflammation. We investigated the effect of a TNF antagonist (adalimumab-ADA) on aortic stiffness in RA patients. We studied...

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Veröffentlicht in:Clinical rheumatology 2015-02, Vol.34 (2), p.359-364
Hauptverfasser: Vassilopoulos, Dimitrios, Gravos, Athanasios, Vlachopoulos, Charalambos, Kandili, Anna, Ioakeimidis, Nikolaos, Pectasides, Dimitrios, Stefanadis, Christodoulos
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container_end_page 364
container_issue 2
container_start_page 359
container_title Clinical rheumatology
container_volume 34
creator Vassilopoulos, Dimitrios
Gravos, Athanasios
Vlachopoulos, Charalambos
Kandili, Anna
Ioakeimidis, Nikolaos
Pectasides, Dimitrios
Stefanadis, Christodoulos
description Rheumatoid arthritis (RA) is associated with increased cardiovascular morbidity and mortality attributed to traditional cardiovascular risk factors and/or the chronic systemic inflammation. We investigated the effect of a TNF antagonist (adalimumab-ADA) on aortic stiffness in RA patients. We studied 18 RA patients with active disease despite therapy with disease modifying antirheumatic drugs (DMARDs), treated with ADA (alone or in combination with DMARDs) for 12 weeks. Disease activity markers as well as aortic stiffness indices (carotid-femoral pulse wave velocity-PWV, augmentation index-AIx), were measured at baseline and at the end of treatment. Eighteen RA patients treated with methotrexate (MTX) were included as controls. Patients were categorized as responders (decrease of Disease Activity Score-DAS28 > 1.2) or nonresponders. There was a statistically significant decrease in PWV (from 8.18 ± 2.03 to 7.01 ± 1.78 m/s, p  = 0.00006) and DAS28 (from 6.65 ± 1.22 to 4.69 ± 1.46, p  = 0.00007) in RA patients treated with ADA. The decrease in PWV was observed both in responders ( n  = 12) and nonresponders ( n  = 6). Multivariate analysis showed that the decrease of PWV was independent of changes in disease activity or other parameters. There was no significant change in PWV in patients treated with MTX (from 8.87 ± 1.91 to 8.41 ± 2.17, p  = 0.29). No significant change in AIx or traditional cardiovascular risk factors was observed. Treatment with ADA significantly reduced aortic stiffness in RA patients regardless of their response to therapy. These findings imply a direct protective effect of ADA in vascular wall in RA patients.
doi_str_mv 10.1007/s10067-014-2718-8
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We investigated the effect of a TNF antagonist (adalimumab-ADA) on aortic stiffness in RA patients. We studied 18 RA patients with active disease despite therapy with disease modifying antirheumatic drugs (DMARDs), treated with ADA (alone or in combination with DMARDs) for 12 weeks. Disease activity markers as well as aortic stiffness indices (carotid-femoral pulse wave velocity-PWV, augmentation index-AIx), were measured at baseline and at the end of treatment. Eighteen RA patients treated with methotrexate (MTX) were included as controls. Patients were categorized as responders (decrease of Disease Activity Score-DAS28 &gt; 1.2) or nonresponders. There was a statistically significant decrease in PWV (from 8.18 ± 2.03 to 7.01 ± 1.78 m/s, p  = 0.00006) and DAS28 (from 6.65 ± 1.22 to 4.69 ± 1.46, p  = 0.00007) in RA patients treated with ADA. The decrease in PWV was observed both in responders ( n  = 12) and nonresponders ( n  = 6). Multivariate analysis showed that the decrease of PWV was independent of changes in disease activity or other parameters. There was no significant change in PWV in patients treated with MTX (from 8.87 ± 1.91 to 8.41 ± 2.17, p  = 0.29). No significant change in AIx or traditional cardiovascular risk factors was observed. Treatment with ADA significantly reduced aortic stiffness in RA patients regardless of their response to therapy. 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We investigated the effect of a TNF antagonist (adalimumab-ADA) on aortic stiffness in RA patients. We studied 18 RA patients with active disease despite therapy with disease modifying antirheumatic drugs (DMARDs), treated with ADA (alone or in combination with DMARDs) for 12 weeks. Disease activity markers as well as aortic stiffness indices (carotid-femoral pulse wave velocity-PWV, augmentation index-AIx), were measured at baseline and at the end of treatment. Eighteen RA patients treated with methotrexate (MTX) were included as controls. Patients were categorized as responders (decrease of Disease Activity Score-DAS28 &gt; 1.2) or nonresponders. There was a statistically significant decrease in PWV (from 8.18 ± 2.03 to 7.01 ± 1.78 m/s, p  = 0.00006) and DAS28 (from 6.65 ± 1.22 to 4.69 ± 1.46, p  = 0.00007) in RA patients treated with ADA. The decrease in PWV was observed both in responders ( n  = 12) and nonresponders ( n  = 6). Multivariate analysis showed that the decrease of PWV was independent of changes in disease activity or other parameters. There was no significant change in PWV in patients treated with MTX (from 8.87 ± 1.91 to 8.41 ± 2.17, p  = 0.29). No significant change in AIx or traditional cardiovascular risk factors was observed. Treatment with ADA significantly reduced aortic stiffness in RA patients regardless of their response to therapy. These findings imply a direct protective effect of ADA in vascular wall in RA patients.</abstract><cop>London</cop><pub>Springer London</pub><pmid>24928345</pmid><doi>10.1007/s10067-014-2718-8</doi><tpages>6</tpages></addata></record>
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subjects Adalimumab
Aged
Antibodies, Monoclonal, Humanized - pharmacology
Antibodies, Monoclonal, Humanized - therapeutic use
Antirheumatic Agents - pharmacology
Antirheumatic Agents - therapeutic use
Arthritis, Rheumatoid - drug therapy
Arthritis, Rheumatoid - physiopathology
Brief Report
Female
Humans
Male
Medicine
Medicine & Public Health
Middle Aged
Rheumatology
Treatment Outcome
Vascular Stiffness - drug effects
Vascular Stiffness - physiology
title Adalimumab decreases aortic stiffness independently of its effect in disease activity in patients with rheumatoid arthritis
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