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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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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. |
format | Online Article Text |
id | pubmed-4452098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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