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Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis
BACKGROUND: Rheumatoid arthritis (RA) is a chronic inflammatory condition characterised by reduced heart rate variability (HRV) of unknown cause. We tested the hypothesis that low HRV, indicative of cardiac autonomic cardiovascular dysfunction, was associated with systemic inflammation and pain. Giv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744865/ https://www.ncbi.nlm.nih.gov/pubmed/28927867 http://dx.doi.org/10.1016/j.autneu.2017.09.003 |
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author | Adlan, Ahmed M. Veldhuijzen van Zanten, Jet J.C.S. Lip, Gregory Y.H. Paton, Julian F.R. Kitas, George D. Fisher, James P. |
author_facet | Adlan, Ahmed M. Veldhuijzen van Zanten, Jet J.C.S. Lip, Gregory Y.H. Paton, Julian F.R. Kitas, George D. Fisher, James P. |
author_sort | Adlan, Ahmed M. |
collection | PubMed |
description | BACKGROUND: Rheumatoid arthritis (RA) is a chronic inflammatory condition characterised by reduced heart rate variability (HRV) of unknown cause. We tested the hypothesis that low HRV, indicative of cardiac autonomic cardiovascular dysfunction, was associated with systemic inflammation and pain. Given the high prevalence of hypertension (HTN) in RA, a condition itself associated with low HRV, we also assessed whether the presence of hypertension further reduced HRV in RA. METHODS: In RA-normotensive (n = 13), RA-HTN (n = 17), normotensive controls (NC; n = 17) and HTN (n = 16) controls, blood pressure and heart rate were recorded. Time and frequency domain measures of HRV along with serological markers of inflammation (high sensitivity C-reactive protein [hs-CRP], tumour necrosis factor-α [TNF-α] and interleukins [IL]) were determined. Reported pain was assessed using a visual analogue scale. RESULTS: Time (rMSSD, pNN50%) and frequency (high frequency power, low frequency power, total power) domain measures of HRV were lower in the RA, RA-HTN and HTN groups, compared to NC (p = 0.001). However, no significant differences in HRV were noted between the RA, RA-HTN and HTN groups. Inverse associations were found between time and frequency measures of HRV and inflammatory cytokines (IL-6 and IL-10), but were not independent after multivariable analysis. hs-CRP and pain were independently and inversely associated with time domain (rMMSD, pNN50%) parameters of HRV. CONCLUSIONS: These findings suggest that lower HRV is associated with increased inflammation and independently associated with increased reported pain, but not compounded by the presence of HTN in patients with RA. |
format | Online Article Text |
id | pubmed-5744865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57448652018-01-02 Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis Adlan, Ahmed M. Veldhuijzen van Zanten, Jet J.C.S. Lip, Gregory Y.H. Paton, Julian F.R. Kitas, George D. Fisher, James P. Auton Neurosci Article BACKGROUND: Rheumatoid arthritis (RA) is a chronic inflammatory condition characterised by reduced heart rate variability (HRV) of unknown cause. We tested the hypothesis that low HRV, indicative of cardiac autonomic cardiovascular dysfunction, was associated with systemic inflammation and pain. Given the high prevalence of hypertension (HTN) in RA, a condition itself associated with low HRV, we also assessed whether the presence of hypertension further reduced HRV in RA. METHODS: In RA-normotensive (n = 13), RA-HTN (n = 17), normotensive controls (NC; n = 17) and HTN (n = 16) controls, blood pressure and heart rate were recorded. Time and frequency domain measures of HRV along with serological markers of inflammation (high sensitivity C-reactive protein [hs-CRP], tumour necrosis factor-α [TNF-α] and interleukins [IL]) were determined. Reported pain was assessed using a visual analogue scale. RESULTS: Time (rMSSD, pNN50%) and frequency (high frequency power, low frequency power, total power) domain measures of HRV were lower in the RA, RA-HTN and HTN groups, compared to NC (p = 0.001). However, no significant differences in HRV were noted between the RA, RA-HTN and HTN groups. Inverse associations were found between time and frequency measures of HRV and inflammatory cytokines (IL-6 and IL-10), but were not independent after multivariable analysis. hs-CRP and pain were independently and inversely associated with time domain (rMMSD, pNN50%) parameters of HRV. CONCLUSIONS: These findings suggest that lower HRV is associated with increased inflammation and independently associated with increased reported pain, but not compounded by the presence of HTN in patients with RA. Elsevier 2017-12 /pmc/articles/PMC5744865/ /pubmed/28927867 http://dx.doi.org/10.1016/j.autneu.2017.09.003 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Adlan, Ahmed M. Veldhuijzen van Zanten, Jet J.C.S. Lip, Gregory Y.H. Paton, Julian F.R. Kitas, George D. Fisher, James P. Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title | Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title_full | Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title_fullStr | Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title_full_unstemmed | Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title_short | Cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
title_sort | cardiovascular autonomic regulation, inflammation and pain in rheumatoid arthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744865/ https://www.ncbi.nlm.nih.gov/pubmed/28927867 http://dx.doi.org/10.1016/j.autneu.2017.09.003 |
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