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Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes

OBJECTIVES: The aims of this study were to investigate circulating levels of inflammatory markers in adolescents with type 1 diabetes with and without different types of neuropathies and evaluate the association between inflammatory biomarkers, nerve function and clinical parameters. DESIGN: Cross-s...

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Autores principales: Rasmussen, Vinni Faber, Hirschberg Jensen, Verena, Thrysøe, Mathilde, Vestergaard, Esben Thyssen, Størling, Joachim, Kristensen, Kurt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565182/
https://www.ncbi.nlm.nih.gov/pubmed/37802616
http://dx.doi.org/10.1136/bmjopen-2023-074992
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author Rasmussen, Vinni Faber
Hirschberg Jensen, Verena
Thrysøe, Mathilde
Vestergaard, Esben Thyssen
Størling, Joachim
Kristensen, Kurt
author_facet Rasmussen, Vinni Faber
Hirschberg Jensen, Verena
Thrysøe, Mathilde
Vestergaard, Esben Thyssen
Størling, Joachim
Kristensen, Kurt
author_sort Rasmussen, Vinni Faber
collection PubMed
description OBJECTIVES: The aims of this study were to investigate circulating levels of inflammatory markers in adolescents with type 1 diabetes with and without different types of neuropathies and evaluate the association between inflammatory biomarkers, nerve function and clinical parameters. DESIGN: Cross-sectional study. SETTING: Hospitals and Steno Diabetes Center in Denmark. PARTICIPANTS: Adolescents with more than 5 years of diabetes duration were investigated for large fibre, small fibre and autonomic neuropathy as a part of the T1DANES study. Blood samples from the participants were analysed for inflammatory biomarkers by Meso Scale Discovery multiplexing technology. PRIMARY AND SECONDARY OUTCOME MEASURES: Inflammatory biomarkers and results of diagnostic nerve tests. RESULTS: Fifty-six adolescents with type 1 diabetes and 23 healthy controls were included. The adolescents with diabetes had significantly higher interferon-gamma, tumour necrosis factor-alpha (TNF-a), interleukin (IL)-10 and soluble urokinase plasminogen activator receptor (suPAR) compared with healthy controls (p values<0.05). TNF-a was higher in the adolescents with large fibre neuropathy (LFN) (p=0.03) compared with those without LFN in the group with diabetes. A negative correlation was seen between TNF-a and conduction velocity in nervus tibialis (p=0.04), and higher TNF-a and IL-6 were associated with higher gastric motility index (TNF-a, p value=0.03; IL-6, p value=0.02). There were no significant associations between inflammatory markers and expressed symptoms, haemoglobin A1c, diabetes duration or body mass index standard derivation score (p values>0.05). The receiver operating characteristic (ROC) curves for the inflammatory markers suggested them as poor screening methods for all types of neuropathies with an area under the curve between 0.47 and 0.67. CONCLUSION: Our results confirm increased low-grade inflammation in adolescents with type 1 diabetes. TNF-a was higher in adolescents with LFN and correlated negatively with nervus tibialis conduction velocity. The other inflammatory biomarkers fail to support differences in those with and without different types of diabetic neuropathies. However, TNF-a and IL-6 were positively correlated to gastric motility index.
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spelling pubmed-105651822023-10-12 Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes Rasmussen, Vinni Faber Hirschberg Jensen, Verena Thrysøe, Mathilde Vestergaard, Esben Thyssen Størling, Joachim Kristensen, Kurt BMJ Open Diabetes and Endocrinology OBJECTIVES: The aims of this study were to investigate circulating levels of inflammatory markers in adolescents with type 1 diabetes with and without different types of neuropathies and evaluate the association between inflammatory biomarkers, nerve function and clinical parameters. DESIGN: Cross-sectional study. SETTING: Hospitals and Steno Diabetes Center in Denmark. PARTICIPANTS: Adolescents with more than 5 years of diabetes duration were investigated for large fibre, small fibre and autonomic neuropathy as a part of the T1DANES study. Blood samples from the participants were analysed for inflammatory biomarkers by Meso Scale Discovery multiplexing technology. PRIMARY AND SECONDARY OUTCOME MEASURES: Inflammatory biomarkers and results of diagnostic nerve tests. RESULTS: Fifty-six adolescents with type 1 diabetes and 23 healthy controls were included. The adolescents with diabetes had significantly higher interferon-gamma, tumour necrosis factor-alpha (TNF-a), interleukin (IL)-10 and soluble urokinase plasminogen activator receptor (suPAR) compared with healthy controls (p values<0.05). TNF-a was higher in the adolescents with large fibre neuropathy (LFN) (p=0.03) compared with those without LFN in the group with diabetes. A negative correlation was seen between TNF-a and conduction velocity in nervus tibialis (p=0.04), and higher TNF-a and IL-6 were associated with higher gastric motility index (TNF-a, p value=0.03; IL-6, p value=0.02). There were no significant associations between inflammatory markers and expressed symptoms, haemoglobin A1c, diabetes duration or body mass index standard derivation score (p values>0.05). The receiver operating characteristic (ROC) curves for the inflammatory markers suggested them as poor screening methods for all types of neuropathies with an area under the curve between 0.47 and 0.67. CONCLUSION: Our results confirm increased low-grade inflammation in adolescents with type 1 diabetes. TNF-a was higher in adolescents with LFN and correlated negatively with nervus tibialis conduction velocity. The other inflammatory biomarkers fail to support differences in those with and without different types of diabetic neuropathies. However, TNF-a and IL-6 were positively correlated to gastric motility index. BMJ Publishing Group 2023-10-06 /pmc/articles/PMC10565182/ /pubmed/37802616 http://dx.doi.org/10.1136/bmjopen-2023-074992 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Diabetes and Endocrinology
Rasmussen, Vinni Faber
Hirschberg Jensen, Verena
Thrysøe, Mathilde
Vestergaard, Esben Thyssen
Størling, Joachim
Kristensen, Kurt
Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title_full Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title_fullStr Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title_full_unstemmed Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title_short Cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
title_sort cross-sectional study investigating the association between inflammatory biomarkers and neuropathy in adolescents with type 1 diabetes
topic Diabetes and Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565182/
https://www.ncbi.nlm.nih.gov/pubmed/37802616
http://dx.doi.org/10.1136/bmjopen-2023-074992
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