Cargando…

Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes

INTRODUCTION: A neuroimmune communication exists, and compelling evidence suggests that diabetic neuropathy and systemic inflammation are linked. Our aims were (1) to investigate biomarkers of the ongoing inflammation processes including cytokines, adhesion molecules, and chemokines and (2) to assoc...

Descripción completa

Detalles Bibliográficos
Autores principales: Wegeberg, Anne-Marie L., Okdahl, Tina, Fløyel, Tina, Brock, Christina, Ejskjaer, Niels, Riahi, Sam, Pociot, Flemming, Størling, Joachim, Brock, Birgitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450314/
https://www.ncbi.nlm.nih.gov/pubmed/32908447
http://dx.doi.org/10.1155/2020/3590389
_version_ 1783574792088059904
author Wegeberg, Anne-Marie L.
Okdahl, Tina
Fløyel, Tina
Brock, Christina
Ejskjaer, Niels
Riahi, Sam
Pociot, Flemming
Størling, Joachim
Brock, Birgitte
author_facet Wegeberg, Anne-Marie L.
Okdahl, Tina
Fløyel, Tina
Brock, Christina
Ejskjaer, Niels
Riahi, Sam
Pociot, Flemming
Størling, Joachim
Brock, Birgitte
author_sort Wegeberg, Anne-Marie L.
collection PubMed
description INTRODUCTION: A neuroimmune communication exists, and compelling evidence suggests that diabetic neuropathy and systemic inflammation are linked. Our aims were (1) to investigate biomarkers of the ongoing inflammation processes including cytokines, adhesion molecules, and chemokines and (2) to associate the findings with cardiovascular autonomic neuropathy in type 1 diabetes by measuring heart rate variability and cardiac vagal tone. MATERIALS AND METHODS: We included 104 adults with type 1 diabetes. Heart rate variability, time domain, and frequency domains were calculated from a 24-hour Holter electrocardiogram, while cardiac vagal tone was determined from a 5-minute electrocardiogram. Cytokines (interleukin- (IL-) 1α, IL-4, IL-12p70, IL-13, IL-17, and tumor necrosis factor- (TNF-) α), adhesion molecules (E-selectin, P-selectin, and intercellular adhesion molecule- (ICAM-) 1), and chemokines (chemokine (C-C motif) ligand (CCL)2, CCL3, CCL4, and C-X-C motif chemokine (CXCL)10) were assessed using a Luminex multiplexing technology. Associations between concentrations of inflammatory biomarkers and continuous variables of heart rate variability and cardiac vagal tone were estimated using multivariable linear regression adjusting for age, sex, disease duration, and smoking. RESULTS: Participants with the presence of cardiovascular autonomic neuropathy had higher systemic levels of IL-1α, IL-4, CCL2, and E-selectin than those without cardiovascular autonomic neuropathy. IL-1α, IL-4, IL-12, TNF-α, and E-selectin were inversely associated with both sympathetic and parasympathetic heart rate variability measures (p > 0.01). Discussion. Our results show that several pro- and anti-inflammatory factors, believed to be involved in the progression of diabetic polyneuropathy, are associated with cardiovascular autonomic neuropathy, suggesting that these factors may also contribute to the pathogenesis of cardiovascular autonomic neuropathy. Our findings emphasize the importance of the neuroimmune regulatory system in the pathogenesis of neuropathy in type 1 diabetes.
format Online
Article
Text
id pubmed-7450314
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-74503142020-09-08 Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes Wegeberg, Anne-Marie L. Okdahl, Tina Fløyel, Tina Brock, Christina Ejskjaer, Niels Riahi, Sam Pociot, Flemming Størling, Joachim Brock, Birgitte Mediators Inflamm Research Article INTRODUCTION: A neuroimmune communication exists, and compelling evidence suggests that diabetic neuropathy and systemic inflammation are linked. Our aims were (1) to investigate biomarkers of the ongoing inflammation processes including cytokines, adhesion molecules, and chemokines and (2) to associate the findings with cardiovascular autonomic neuropathy in type 1 diabetes by measuring heart rate variability and cardiac vagal tone. MATERIALS AND METHODS: We included 104 adults with type 1 diabetes. Heart rate variability, time domain, and frequency domains were calculated from a 24-hour Holter electrocardiogram, while cardiac vagal tone was determined from a 5-minute electrocardiogram. Cytokines (interleukin- (IL-) 1α, IL-4, IL-12p70, IL-13, IL-17, and tumor necrosis factor- (TNF-) α), adhesion molecules (E-selectin, P-selectin, and intercellular adhesion molecule- (ICAM-) 1), and chemokines (chemokine (C-C motif) ligand (CCL)2, CCL3, CCL4, and C-X-C motif chemokine (CXCL)10) were assessed using a Luminex multiplexing technology. Associations between concentrations of inflammatory biomarkers and continuous variables of heart rate variability and cardiac vagal tone were estimated using multivariable linear regression adjusting for age, sex, disease duration, and smoking. RESULTS: Participants with the presence of cardiovascular autonomic neuropathy had higher systemic levels of IL-1α, IL-4, CCL2, and E-selectin than those without cardiovascular autonomic neuropathy. IL-1α, IL-4, IL-12, TNF-α, and E-selectin were inversely associated with both sympathetic and parasympathetic heart rate variability measures (p > 0.01). Discussion. Our results show that several pro- and anti-inflammatory factors, believed to be involved in the progression of diabetic polyneuropathy, are associated with cardiovascular autonomic neuropathy, suggesting that these factors may also contribute to the pathogenesis of cardiovascular autonomic neuropathy. Our findings emphasize the importance of the neuroimmune regulatory system in the pathogenesis of neuropathy in type 1 diabetes. Hindawi 2020-08-18 /pmc/articles/PMC7450314/ /pubmed/32908447 http://dx.doi.org/10.1155/2020/3590389 Text en Copyright © 2020 Anne-Marie L. Wegeberg et al. http://creativecommons.org/licenses/by/4.0/ 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 Research Article
Wegeberg, Anne-Marie L.
Okdahl, Tina
Fløyel, Tina
Brock, Christina
Ejskjaer, Niels
Riahi, Sam
Pociot, Flemming
Størling, Joachim
Brock, Birgitte
Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title_full Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title_fullStr Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title_full_unstemmed Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title_short Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
title_sort circulating inflammatory markers are inversely associated with heart rate variability measures in type 1 diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450314/
https://www.ncbi.nlm.nih.gov/pubmed/32908447
http://dx.doi.org/10.1155/2020/3590389
work_keys_str_mv AT wegebergannemariel circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT okdahltina circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT fløyeltina circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT brockchristina circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT ejskjaerniels circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT riahisam circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT pociotflemming circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT størlingjoachim circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT brockbirgitte circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes