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Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity

Systemic inflammation and disease activity seem to contribute to excessive prevalence of cardiovascular (CV) diseases (CVDs) in patients with rheumatoid arthritis (RA). The objective of the study was to assess chosen CV parameters in RA patients who have continuous low disease activity. The study gr...

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Autores principales: Biskup, Małgorzata, Biskup, Wojciech, Majdan, Maria, Targońska-Stępniak, Bożena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006198/
https://www.ncbi.nlm.nih.gov/pubmed/29774373
http://dx.doi.org/10.1007/s00296-018-4053-x
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author Biskup, Małgorzata
Biskup, Wojciech
Majdan, Maria
Targońska-Stępniak, Bożena
author_facet Biskup, Małgorzata
Biskup, Wojciech
Majdan, Maria
Targońska-Stępniak, Bożena
author_sort Biskup, Małgorzata
collection PubMed
description Systemic inflammation and disease activity seem to contribute to excessive prevalence of cardiovascular (CV) diseases (CVDs) in patients with rheumatoid arthritis (RA). The objective of the study was to assess chosen CV parameters in RA patients who have continuous low disease activity. The study group consisted of 70 RA patients without known CVD and 33 healthy controls, of a comparable age. All RA patients had continued low disease activity (DAS28 ≤ 3.2) from 2 to 7 years. The groups were assessed for: blood pressure, serum amino-terminal pro-brain natriuretic peptide (NT-proBNP), carotid intima media thickness (cIMT), electrocardiography (ECG), ejection fraction (EJ) and diastolic dysfunction (E/A ratio) in echocardiography. In RA patients in comparison with controls, significantly greater values of cIMT [0.83 (0.21) vs 0.62 (0.1) mm, p < 0.001] were found, as well as higher incidence of atherosclerotic plaques [43 (61.4%) vs 10 (30.3%), p = 0.003], prolonged QTc interval [439.6 (23.7) vs 414.0 (27.9) ms, p < 0.001]. High or very high Systemic Coronary Risk Evaluation (SCORE) was found in 32.9% of patients with RA and increased serum NT-proBNP in 71.4%. The mean values of CV parameters (cIMT, E/A, NT-proBNP, SCORE) were associated with age, disease duration, rheumatoid factor (RF-IgM), erythrocyte sedimentation rate (ESR). The results of our study indicate, that RA with continued low disease activity is associated with atherosclerosis and heart dysfunction. Strong relationships were found between CV parameters and patients’ age, disease duration. Deterioration of CV parameters was associated with higher DAS28, ESR, RF-IgM concentration and bone erosions.
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spelling pubmed-60061982018-07-04 Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity Biskup, Małgorzata Biskup, Wojciech Majdan, Maria Targońska-Stępniak, Bożena Rheumatol Int Comorbidities Systemic inflammation and disease activity seem to contribute to excessive prevalence of cardiovascular (CV) diseases (CVDs) in patients with rheumatoid arthritis (RA). The objective of the study was to assess chosen CV parameters in RA patients who have continuous low disease activity. The study group consisted of 70 RA patients without known CVD and 33 healthy controls, of a comparable age. All RA patients had continued low disease activity (DAS28 ≤ 3.2) from 2 to 7 years. The groups were assessed for: blood pressure, serum amino-terminal pro-brain natriuretic peptide (NT-proBNP), carotid intima media thickness (cIMT), electrocardiography (ECG), ejection fraction (EJ) and diastolic dysfunction (E/A ratio) in echocardiography. In RA patients in comparison with controls, significantly greater values of cIMT [0.83 (0.21) vs 0.62 (0.1) mm, p < 0.001] were found, as well as higher incidence of atherosclerotic plaques [43 (61.4%) vs 10 (30.3%), p = 0.003], prolonged QTc interval [439.6 (23.7) vs 414.0 (27.9) ms, p < 0.001]. High or very high Systemic Coronary Risk Evaluation (SCORE) was found in 32.9% of patients with RA and increased serum NT-proBNP in 71.4%. The mean values of CV parameters (cIMT, E/A, NT-proBNP, SCORE) were associated with age, disease duration, rheumatoid factor (RF-IgM), erythrocyte sedimentation rate (ESR). The results of our study indicate, that RA with continued low disease activity is associated with atherosclerosis and heart dysfunction. Strong relationships were found between CV parameters and patients’ age, disease duration. Deterioration of CV parameters was associated with higher DAS28, ESR, RF-IgM concentration and bone erosions. Springer Berlin Heidelberg 2018-05-17 2018 /pmc/articles/PMC6006198/ /pubmed/29774373 http://dx.doi.org/10.1007/s00296-018-4053-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Comorbidities
Biskup, Małgorzata
Biskup, Wojciech
Majdan, Maria
Targońska-Stępniak, Bożena
Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title_full Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title_fullStr Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title_full_unstemmed Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title_short Cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
title_sort cardiovascular system changes in rheumatoid arthritis patients with continued low disease activity
topic Comorbidities
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006198/
https://www.ncbi.nlm.nih.gov/pubmed/29774373
http://dx.doi.org/10.1007/s00296-018-4053-x
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