Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784570691626991616 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8455555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT januszewskiandrzejs relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT chendavid relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT scottrussells relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT oconnellrachell relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT aryalnandar relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT sullivandavidr relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT wattsgeraldf relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT taskinenmarjariitta relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT barterphilipj relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT bestjamesd relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT simesrjohn relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT keechanthonyc relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes AT jenkinsaliciaj relationshipoflowmolecularweightfluorophorelevelswithclinicalfactorsandfenofibrateeffectsinadultswithtype2diabetes |