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...

Full description

Saved in:
Bibliographic Details
Main Authors: Anne-Marie L. Wegeberg, Tina Okdahl, Tina Fløyel, Christina Brock, Niels Ejskjaer, Sam Riahi, Flemming Pociot, Joachim Størling, Birgitte Brock
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2020/3590389
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832566147469279232
author Anne-Marie L. Wegeberg
Tina Okdahl
Tina Fløyel
Christina Brock
Niels Ejskjaer
Sam Riahi
Flemming Pociot
Joachim Størling
Birgitte Brock
author_facet Anne-Marie L. Wegeberg
Tina Okdahl
Tina Fløyel
Christina Brock
Niels Ejskjaer
Sam Riahi
Flemming Pociot
Joachim Størling
Birgitte Brock
author_sort Anne-Marie L. Wegeberg
collection DOAJ
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 Article
id doaj-art-93db61001a75463a97765521ab536afb
institution Kabale University
issn 0962-9351
1466-1861
language English
publishDate 2020-01-01
publisher Wiley
record_format Article
series Mediators of Inflammation
spelling doaj-art-93db61001a75463a97765521ab536afb2025-02-03T01:05:02ZengWileyMediators of Inflammation0962-93511466-18612020-01-01202010.1155/2020/35903893590389Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 DiabetesAnne-Marie L. Wegeberg0Tina Okdahl1Tina Fløyel2Christina Brock3Niels Ejskjaer4Sam Riahi5Flemming Pociot6Joachim Størling7Birgitte Brock8Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, DenmarkMech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, DenmarkSteno Diabetes Center Copenhagen, Gentofte, DenmarkMech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, DenmarkClinical Institute, Aalborg University, Aalborg, DenmarkDepartment of Cardiology, Aalborg University Hospital, DenmarkSteno Diabetes Center Copenhagen, Gentofte, DenmarkSteno Diabetes Center Copenhagen, Gentofte, DenmarkSteno Diabetes Center Copenhagen, Gentofte, DenmarkIntroduction. 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.http://dx.doi.org/10.1155/2020/3590389
spellingShingle Anne-Marie L. Wegeberg
Tina Okdahl
Tina Fløyel
Christina Brock
Niels Ejskjaer
Sam Riahi
Flemming Pociot
Joachim Størling
Birgitte Brock
Circulating Inflammatory Markers Are Inversely Associated with Heart Rate Variability Measures in Type 1 Diabetes
Mediators of Inflammation
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
url http://dx.doi.org/10.1155/2020/3590389
work_keys_str_mv AT annemarielwegeberg circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT tinaokdahl circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT tinafløyel circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT christinabrock circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT nielsejskjaer circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT samriahi circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT flemmingpociot circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT joachimstørling circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes
AT birgittebrock circulatinginflammatorymarkersareinverselyassociatedwithheartratevariabilitymeasuresintype1diabetes