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Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis

Little is known about the interplay between the autonomic nervous system and disease activity in multiple sclerosis (MS). We examined the relationship between heart rate variability (HRV), a reliable measure of vagal nerve function, and disease characteristics in a prospective MS cohort. Standard de...

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Autores principales: Reynders, Tatjana, Gidron, Yori, De Ville, Jella, Bjerke, Maria, Weets, Ilse, Van Remoortel, Ann, Devolder, Lindsay, D’haeseleer, Miguel, De Keyser, Jacques, Nagels, Guy, D’hooghe, Marie B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019937/
https://www.ncbi.nlm.nih.gov/pubmed/31861312
http://dx.doi.org/10.3390/jcm9010003
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author Reynders, Tatjana
Gidron, Yori
De Ville, Jella
Bjerke, Maria
Weets, Ilse
Van Remoortel, Ann
Devolder, Lindsay
D’haeseleer, Miguel
De Keyser, Jacques
Nagels, Guy
D’hooghe, Marie B.
author_facet Reynders, Tatjana
Gidron, Yori
De Ville, Jella
Bjerke, Maria
Weets, Ilse
Van Remoortel, Ann
Devolder, Lindsay
D’haeseleer, Miguel
De Keyser, Jacques
Nagels, Guy
D’hooghe, Marie B.
author_sort Reynders, Tatjana
collection PubMed
description Little is known about the interplay between the autonomic nervous system and disease activity in multiple sclerosis (MS). We examined the relationship between heart rate variability (HRV), a reliable measure of vagal nerve function, and disease characteristics in a prospective MS cohort. Standard deviation of each normal-to-normal inter-beat interval (SDNN) and root mean square of successive differences (RMSSD), global indices of HRV, were measured in 114 MS patients, which included four predefined subgroups, and 30 age and sex-matched healthy controls (HC). We assessed group differences at baseline, HRV reproducibility at month 3, and used logistic regression modeling to relate baseline HRV with relapse occurrence. No significant HRV differences were found between MS and HC and between MS subgroups. In MS patients, both HRV indices correlated with age (r = −0.278, p = 0.018 and r = −0.319, p < 0.001, respectively) and with month 3 assessments (r = 0.695 and r = 0.760, p < 0.001). Higher SDNN and RMSSD at baseline were associated with self-reported relapses at month 3 (OR = 1.053, 95% CI (1.013–1.095), p = 0.009 and OR = 1.065, 95% CI (1.016–1.117), p = 0.009), and SDNN at baseline with relapses at month 12 (OR = 1.034, 95% CI (1.009–1.059), p = 0.008; ROC, AUC = 0.733, p = 0.002). There were no baseline HRV differences between MS and HC or between subgroups. Post-hoc analysis showed an association with an increased relapse risk.
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spelling pubmed-70199372020-03-09 Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis Reynders, Tatjana Gidron, Yori De Ville, Jella Bjerke, Maria Weets, Ilse Van Remoortel, Ann Devolder, Lindsay D’haeseleer, Miguel De Keyser, Jacques Nagels, Guy D’hooghe, Marie B. J Clin Med Article Little is known about the interplay between the autonomic nervous system and disease activity in multiple sclerosis (MS). We examined the relationship between heart rate variability (HRV), a reliable measure of vagal nerve function, and disease characteristics in a prospective MS cohort. Standard deviation of each normal-to-normal inter-beat interval (SDNN) and root mean square of successive differences (RMSSD), global indices of HRV, were measured in 114 MS patients, which included four predefined subgroups, and 30 age and sex-matched healthy controls (HC). We assessed group differences at baseline, HRV reproducibility at month 3, and used logistic regression modeling to relate baseline HRV with relapse occurrence. No significant HRV differences were found between MS and HC and between MS subgroups. In MS patients, both HRV indices correlated with age (r = −0.278, p = 0.018 and r = −0.319, p < 0.001, respectively) and with month 3 assessments (r = 0.695 and r = 0.760, p < 0.001). Higher SDNN and RMSSD at baseline were associated with self-reported relapses at month 3 (OR = 1.053, 95% CI (1.013–1.095), p = 0.009 and OR = 1.065, 95% CI (1.016–1.117), p = 0.009), and SDNN at baseline with relapses at month 12 (OR = 1.034, 95% CI (1.009–1.059), p = 0.008; ROC, AUC = 0.733, p = 0.002). There were no baseline HRV differences between MS and HC or between subgroups. Post-hoc analysis showed an association with an increased relapse risk. MDPI 2019-12-18 /pmc/articles/PMC7019937/ /pubmed/31861312 http://dx.doi.org/10.3390/jcm9010003 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reynders, Tatjana
Gidron, Yori
De Ville, Jella
Bjerke, Maria
Weets, Ilse
Van Remoortel, Ann
Devolder, Lindsay
D’haeseleer, Miguel
De Keyser, Jacques
Nagels, Guy
D’hooghe, Marie B.
Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title_full Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title_fullStr Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title_full_unstemmed Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title_short Relation between Heart Rate Variability and Disease Course in Multiple Sclerosis
title_sort relation between heart rate variability and disease course in multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019937/
https://www.ncbi.nlm.nih.gov/pubmed/31861312
http://dx.doi.org/10.3390/jcm9010003
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