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Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis

Introduction. The risk of cardiovascular disease is increased in rheumatoid arthritis (RA). A meta-analysis showed increased intima media thickness (IMT) in RA. It has been shown that disease modifying antirheumatic drugs (DMARDs) may influence the progression of atherosclerosis. However, it was sug...

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Autores principales: Kisiel, Bartłomiej, Kruszewski, Robert, Juszkiewicz, Aleksandra, Raczkiewicz, Anna, Bachta, Artur, Tłustochowicz, Małgorzata, Staniszewska-Varga, Jadwiga, Kłos, Krzysztof, Duda, Krzysztof, Bogusławska-Walecka, Romana, Płoski, Rafał, Tłustochowicz, Witold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452098/
https://www.ncbi.nlm.nih.gov/pubmed/26090499
http://dx.doi.org/10.1155/2015/759610
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author Kisiel, Bartłomiej
Kruszewski, Robert
Juszkiewicz, Aleksandra
Raczkiewicz, Anna
Bachta, Artur
Tłustochowicz, Małgorzata
Staniszewska-Varga, Jadwiga
Kłos, Krzysztof
Duda, Krzysztof
Bogusławska-Walecka, Romana
Płoski, Rafał
Tłustochowicz, Witold
author_facet Kisiel, Bartłomiej
Kruszewski, Robert
Juszkiewicz, Aleksandra
Raczkiewicz, Anna
Bachta, Artur
Tłustochowicz, Małgorzata
Staniszewska-Varga, Jadwiga
Kłos, Krzysztof
Duda, Krzysztof
Bogusławska-Walecka, Romana
Płoski, Rafał
Tłustochowicz, Witold
author_sort Kisiel, Bartłomiej
collection PubMed
description Introduction. The risk of cardiovascular disease is increased in rheumatoid arthritis (RA). A meta-analysis showed increased intima media thickness (IMT) in RA. It has been shown that disease modifying antirheumatic drugs (DMARDs) may influence the progression of atherosclerosis. However, it was suggested that biologics may be more efficient than other DMARDs (including methotrexate—MTX) in protecting against atherosclerosis. Objectives. The aim of this study was to assess the influence of different RA characteristics and treatment regimens on IMT and atherosclerotic plaques. Patients and Methods. 317 RA patients and 111 controls were included in the study. IMT was measured in carotid (CIMT) and femoral (FIMT) arteries. Arteries were screened for the presence of plaques. Results. CIMT, FIMT, and prevalence of plaques were lower in patients treated with methotrexate (MTX) ≥ 20 mg/wk, cyclosporine (CsA), or biologics than in patients treated with lower doses of MTX and other disease modifying antirheumatic drugs. No differences in IMT between patients treated with MTX ≥ 20 mg/wk, biologics, or CsA were found. Conclusions. We found a beneficial effect of MTX ≥ 20 mg/wk, biologics, and CsA on atherosclerosis. We do not confirm a stronger influence of biologics on IMT compared with therapeutic doses of MTX.
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spelling pubmed-44520982015-06-18 Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis Kisiel, Bartłomiej Kruszewski, Robert Juszkiewicz, Aleksandra Raczkiewicz, Anna Bachta, Artur Tłustochowicz, Małgorzata Staniszewska-Varga, Jadwiga Kłos, Krzysztof Duda, Krzysztof Bogusławska-Walecka, Romana Płoski, Rafał Tłustochowicz, Witold J Immunol Res Clinical Study Introduction. The risk of cardiovascular disease is increased in rheumatoid arthritis (RA). A meta-analysis showed increased intima media thickness (IMT) in RA. It has been shown that disease modifying antirheumatic drugs (DMARDs) may influence the progression of atherosclerosis. However, it was suggested that biologics may be more efficient than other DMARDs (including methotrexate—MTX) in protecting against atherosclerosis. Objectives. The aim of this study was to assess the influence of different RA characteristics and treatment regimens on IMT and atherosclerotic plaques. Patients and Methods. 317 RA patients and 111 controls were included in the study. IMT was measured in carotid (CIMT) and femoral (FIMT) arteries. Arteries were screened for the presence of plaques. Results. CIMT, FIMT, and prevalence of plaques were lower in patients treated with methotrexate (MTX) ≥ 20 mg/wk, cyclosporine (CsA), or biologics than in patients treated with lower doses of MTX and other disease modifying antirheumatic drugs. No differences in IMT between patients treated with MTX ≥ 20 mg/wk, biologics, or CsA were found. Conclusions. We found a beneficial effect of MTX ≥ 20 mg/wk, biologics, and CsA on atherosclerosis. We do not confirm a stronger influence of biologics on IMT compared with therapeutic doses of MTX. Hindawi Publishing Corporation 2015 2015-05-18 /pmc/articles/PMC4452098/ /pubmed/26090499 http://dx.doi.org/10.1155/2015/759610 Text en Copyright © 2015 Bartłomiej Kisiel et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Kisiel, Bartłomiej
Kruszewski, Robert
Juszkiewicz, Aleksandra
Raczkiewicz, Anna
Bachta, Artur
Tłustochowicz, Małgorzata
Staniszewska-Varga, Jadwiga
Kłos, Krzysztof
Duda, Krzysztof
Bogusławska-Walecka, Romana
Płoski, Rafał
Tłustochowicz, Witold
Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title_full Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title_fullStr Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title_full_unstemmed Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title_short Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis
title_sort methotrexate, cyclosporine a, and biologics protect against atherosclerosis in rheumatoid arthritis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452098/
https://www.ncbi.nlm.nih.gov/pubmed/26090499
http://dx.doi.org/10.1155/2015/759610
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