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Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes

People with diabetes are at risk of chronic complications and novel biomarkers, such as Advanced glycation end-products (AGEs) may help stratify this risk. We assessed whether plasma low-molecular weight AGEs, also known as LMW-fluorophores (LMW-F), are associated with risk factors, predict complica...

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Autores principales: Januszewski, Andrzej S., Chen, David, Scott, Russell S., O’Connell, Rachel L., Aryal, Nanda R., Sullivan, David R., Watts, Gerald F., Taskinen, Marja-Riitta, Barter, Philip J., Best, James D., Simes, R. John, Keech, Anthony C., Jenkins, Alicia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455555/
https://www.ncbi.nlm.nih.gov/pubmed/34548531
http://dx.doi.org/10.1038/s41598-021-98064-y
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author Januszewski, Andrzej S.
Chen, David
Scott, Russell S.
O’Connell, Rachel L.
Aryal, Nanda R.
Sullivan, David R.
Watts, Gerald F.
Taskinen, Marja-Riitta
Barter, Philip J.
Best, James D.
Simes, R. John
Keech, Anthony C.
Jenkins, Alicia J.
author_facet Januszewski, Andrzej S.
Chen, David
Scott, Russell S.
O’Connell, Rachel L.
Aryal, Nanda R.
Sullivan, David R.
Watts, Gerald F.
Taskinen, Marja-Riitta
Barter, Philip J.
Best, James D.
Simes, R. John
Keech, Anthony C.
Jenkins, Alicia J.
author_sort Januszewski, Andrzej S.
collection PubMed
description People with diabetes are at risk of chronic complications and novel biomarkers, such as Advanced glycation end-products (AGEs) may help stratify this risk. We assessed whether plasma low-molecular weight AGEs, also known as LMW-fluorophores (LMW-F), are associated with risk factors, predict complications, and are altered by fenofibrate in adults with type 2 diabetes. Plasma LMW-F were quantified at baseline, after six weeks fenofibrate, and one year post-randomisation to fenofibrate or placebo. LMW-F associations with existing and new composite vascular complications were determined, and effects of fenofibrate assessed. LMW-F correlated positively with age, glycated haemoglobin (HbA1c), pulse pressure, kidney dysfunction and inflammation; and negatively with urate, body mass index, oxidative stress and leptin, albeit weakly (r = 0.04–0.16, all p < 0.01). Independent determinants of LMW-F included smoking, diastolic blood pressure, prior cardiovascular disease or microvascular complications, Caucasian ethnicity, kidney function, HbA1c and diabetes duration (all p ≤ 0.01). Baseline LMW-F tertiles correlated with on-trial macrovascular and microvascular complications (trend p < 0.001) on univariate analyses only. Six weeks of fenofibrate increased LMW-F levels by 21% (p < 0.001). In conclusion, LMW-F levels correlate with many risk factors and chronic diabetes complications, and are increased with fenofibrate. LMW-F tertiles predict complications, but not independently of traditional risk factors.
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spelling pubmed-84555552021-09-22 Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes Januszewski, Andrzej S. Chen, David Scott, Russell S. O’Connell, Rachel L. Aryal, Nanda R. Sullivan, David R. Watts, Gerald F. Taskinen, Marja-Riitta Barter, Philip J. Best, James D. Simes, R. John Keech, Anthony C. Jenkins, Alicia J. Sci Rep Article People with diabetes are at risk of chronic complications and novel biomarkers, such as Advanced glycation end-products (AGEs) may help stratify this risk. We assessed whether plasma low-molecular weight AGEs, also known as LMW-fluorophores (LMW-F), are associated with risk factors, predict complications, and are altered by fenofibrate in adults with type 2 diabetes. Plasma LMW-F were quantified at baseline, after six weeks fenofibrate, and one year post-randomisation to fenofibrate or placebo. LMW-F associations with existing and new composite vascular complications were determined, and effects of fenofibrate assessed. LMW-F correlated positively with age, glycated haemoglobin (HbA1c), pulse pressure, kidney dysfunction and inflammation; and negatively with urate, body mass index, oxidative stress and leptin, albeit weakly (r = 0.04–0.16, all p < 0.01). Independent determinants of LMW-F included smoking, diastolic blood pressure, prior cardiovascular disease or microvascular complications, Caucasian ethnicity, kidney function, HbA1c and diabetes duration (all p ≤ 0.01). Baseline LMW-F tertiles correlated with on-trial macrovascular and microvascular complications (trend p < 0.001) on univariate analyses only. Six weeks of fenofibrate increased LMW-F levels by 21% (p < 0.001). In conclusion, LMW-F levels correlate with many risk factors and chronic diabetes complications, and are increased with fenofibrate. LMW-F tertiles predict complications, but not independently of traditional risk factors. Nature Publishing Group UK 2021-09-21 /pmc/articles/PMC8455555/ /pubmed/34548531 http://dx.doi.org/10.1038/s41598-021-98064-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Januszewski, Andrzej S.
Chen, David
Scott, Russell S.
O’Connell, Rachel L.
Aryal, Nanda R.
Sullivan, David R.
Watts, Gerald F.
Taskinen, Marja-Riitta
Barter, Philip J.
Best, James D.
Simes, R. John
Keech, Anthony C.
Jenkins, Alicia J.
Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title_full Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title_fullStr Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title_full_unstemmed Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title_short Relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
title_sort relationship of low molecular weight fluorophore levels with clinical factors and fenofibrate effects in adults with type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455555/
https://www.ncbi.nlm.nih.gov/pubmed/34548531
http://dx.doi.org/10.1038/s41598-021-98064-y
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