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Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease

BACKGROUND: Alterations in autonomic nervous function are common in hemodialysis (HD) patients. Sympathetic as well as parasympathetic activation may be associated with immune and inflammatory responses. We intended to confirm a role of autonomous dysregulation for inflammation in HD patients. METHO...

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Autores principales: Seibert, Eric, Zohles, Kristina, Ulrich, Christof, Kluttig, Alexander, Nuding, Sebastian, Kors, Jan A., Swenne, Cees A., Werdan, Karl, Fiedler, Roman, Girndt, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094069/
https://www.ncbi.nlm.nih.gov/pubmed/27809785
http://dx.doi.org/10.1186/s12872-016-0385-1
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author Seibert, Eric
Zohles, Kristina
Ulrich, Christof
Kluttig, Alexander
Nuding, Sebastian
Kors, Jan A.
Swenne, Cees A.
Werdan, Karl
Fiedler, Roman
Girndt, Matthias
author_facet Seibert, Eric
Zohles, Kristina
Ulrich, Christof
Kluttig, Alexander
Nuding, Sebastian
Kors, Jan A.
Swenne, Cees A.
Werdan, Karl
Fiedler, Roman
Girndt, Matthias
author_sort Seibert, Eric
collection PubMed
description BACKGROUND: Alterations in autonomic nervous function are common in hemodialysis (HD) patients. Sympathetic as well as parasympathetic activation may be associated with immune and inflammatory responses. We intended to confirm a role of autonomous dysregulation for inflammation in HD patients. METHODS: 30 HD patients (including 15 diabetics) and 15 healthy controls were studied for heart rate variability (HRV) using 5 min ECG recordings. Heart rate variability was estimated by time-domain parameters (the standard deviation of the RR intervals (SDNN) and the percentage of pairs of adjacent RR intervals differing by >50 ms (pNN50)) and frequency-domain-analysis (high- and low-frequency variation of RR intervals, HF and LF). Inflammation was detected as serum C-reactive Protein (CRP), IL-6 and circulating monocyte subpopulation numbers. Immune cells were characterized by ACh receptor expression. RESULTS: Patients differed from controls in terms of age (68.0 [14.8] yrs vs. 58.0 [13.0] yrs, p < 0.001; Median [IQR]) and sex. However, HRV parameters were different in controls and HD patients (SDNN controls 34.0 [14.0] ms, HD patients 15.5 [14.8] ms, p < 0.01). This finding was not restricted to patients with diabetes mellitus (diab), although diabetes is an important cause of autonomous dysfunction (SDNN, diab 13.0 [14.0] ms, non-diab 18.0 [15.3] ms, p = 0.8). LF and HF were reduced by the same magnitude to 1/3 of those in controls. Patients suffered from chronic inflammation (CRP 9.4 [12.9] mg/l, controls 1.6 [2.4] mg/l, p < 0.001) and expanded proinflammatory monocyte subpopulations (CD14++/CD16+ cells: patients 41 [27]/μl, controls 24 [18]/μl, p < 0.01). ECG parameters did not correlate with inflammation in patients, but monocyte ACh receptor expression was enhanced, indicating potentially elevated responsiveness of this cell type to parasympathetic regulation. CONCLUSIONS: HD patients have strongly impaired HRV. Chronic inflammation is not related to autonomous dysfunction, although monocytes express the ACh receptor at enhanced density making them potentially more sensitive to parasympathetic effects. TRIAL REGISTRATION: This study was listed with ClinicalTrials.gov (NCT00878033). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12872-016-0385-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-50940692016-11-07 Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease Seibert, Eric Zohles, Kristina Ulrich, Christof Kluttig, Alexander Nuding, Sebastian Kors, Jan A. Swenne, Cees A. Werdan, Karl Fiedler, Roman Girndt, Matthias BMC Cardiovasc Disord Research Article BACKGROUND: Alterations in autonomic nervous function are common in hemodialysis (HD) patients. Sympathetic as well as parasympathetic activation may be associated with immune and inflammatory responses. We intended to confirm a role of autonomous dysregulation for inflammation in HD patients. METHODS: 30 HD patients (including 15 diabetics) and 15 healthy controls were studied for heart rate variability (HRV) using 5 min ECG recordings. Heart rate variability was estimated by time-domain parameters (the standard deviation of the RR intervals (SDNN) and the percentage of pairs of adjacent RR intervals differing by >50 ms (pNN50)) and frequency-domain-analysis (high- and low-frequency variation of RR intervals, HF and LF). Inflammation was detected as serum C-reactive Protein (CRP), IL-6 and circulating monocyte subpopulation numbers. Immune cells were characterized by ACh receptor expression. RESULTS: Patients differed from controls in terms of age (68.0 [14.8] yrs vs. 58.0 [13.0] yrs, p < 0.001; Median [IQR]) and sex. However, HRV parameters were different in controls and HD patients (SDNN controls 34.0 [14.0] ms, HD patients 15.5 [14.8] ms, p < 0.01). This finding was not restricted to patients with diabetes mellitus (diab), although diabetes is an important cause of autonomous dysfunction (SDNN, diab 13.0 [14.0] ms, non-diab 18.0 [15.3] ms, p = 0.8). LF and HF were reduced by the same magnitude to 1/3 of those in controls. Patients suffered from chronic inflammation (CRP 9.4 [12.9] mg/l, controls 1.6 [2.4] mg/l, p < 0.001) and expanded proinflammatory monocyte subpopulations (CD14++/CD16+ cells: patients 41 [27]/μl, controls 24 [18]/μl, p < 0.01). ECG parameters did not correlate with inflammation in patients, but monocyte ACh receptor expression was enhanced, indicating potentially elevated responsiveness of this cell type to parasympathetic regulation. CONCLUSIONS: HD patients have strongly impaired HRV. Chronic inflammation is not related to autonomous dysfunction, although monocytes express the ACh receptor at enhanced density making them potentially more sensitive to parasympathetic effects. TRIAL REGISTRATION: This study was listed with ClinicalTrials.gov (NCT00878033). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12872-016-0385-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-03 /pmc/articles/PMC5094069/ /pubmed/27809785 http://dx.doi.org/10.1186/s12872-016-0385-1 Text en © The Author(s). 2016 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Seibert, Eric
Zohles, Kristina
Ulrich, Christof
Kluttig, Alexander
Nuding, Sebastian
Kors, Jan A.
Swenne, Cees A.
Werdan, Karl
Fiedler, Roman
Girndt, Matthias
Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title_full Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title_fullStr Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title_full_unstemmed Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title_short Association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
title_sort association between autonomic nervous dysfunction and cellular inflammation in end-stage renal disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094069/
https://www.ncbi.nlm.nih.gov/pubmed/27809785
http://dx.doi.org/10.1186/s12872-016-0385-1
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