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Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes

BACKGROUND: Circulating microRNAs are emerging as potential prognostic biomarkers for the development of type 2 diabetes. However, microRNAs are also associated with complications from impaired glucose metabolism (e.g. endothelial cell function). Prior studies have not evaluated for associations bet...

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Autores principales: Flowers, E., Kanaya, A. M., Fukuoka, Y., Allen, I. E., Cooper, B., Aouizerat, B. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729496/
https://www.ncbi.nlm.nih.gov/pubmed/29259803
http://dx.doi.org/10.1002/osp4.134
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author Flowers, E.
Kanaya, A. M.
Fukuoka, Y.
Allen, I. E.
Cooper, B.
Aouizerat, B. E.
author_facet Flowers, E.
Kanaya, A. M.
Fukuoka, Y.
Allen, I. E.
Cooper, B.
Aouizerat, B. E.
author_sort Flowers, E.
collection PubMed
description BACKGROUND: Circulating microRNAs are emerging as potential prognostic biomarkers for the development of type 2 diabetes. However, microRNAs are also associated with complications from impaired glucose metabolism (e.g. endothelial cell function). Prior studies have not evaluated for associations between trajectories of circulating microRNAs with trajectories of fasting blood glucose over time and the responses to behavioral interventions to reduce risk. This study performed longitudinal assessment of microRNAs and fasting blood glucose and identified relationships between microRNAs and behavioral risk reduction interventions. METHODS: MicroRNAs (n = 353) were measured in subsets (n = 10, n = 8) of participants from previously completed clinical trials that studied behavioral risk reduction interventions. Fasting blood glucose trajectories were associated with changes in 45 microRNAs over 12 months. RESULTS: Following a 3‐month physical activity and dietary intervention compared with baseline, 13 microRNAs were differentially expressed. Seven microRNAs (i.e. miR‐106b, miR‐20b, miR‐363, miR‐486, miR‐532, miR‐92a and miR‐93) were commonly identified between the two analyses. CONCLUSIONS: Further studies are needed to determine which microRNAs are prognostic biomarkers of risk for type 2 diabetes versus consequences of impaired glucose metabolism. Additional future directions of this research are to differentiate whether microRNAs are prognostic and/or diagnostic biomarkers for risk for type 2 diabetes and predictive biomarkers of responses to risk reduction interventions.
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spelling pubmed-57294962017-12-19 Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes Flowers, E. Kanaya, A. M. Fukuoka, Y. Allen, I. E. Cooper, B. Aouizerat, B. E. Obes Sci Pract Short Communications BACKGROUND: Circulating microRNAs are emerging as potential prognostic biomarkers for the development of type 2 diabetes. However, microRNAs are also associated with complications from impaired glucose metabolism (e.g. endothelial cell function). Prior studies have not evaluated for associations between trajectories of circulating microRNAs with trajectories of fasting blood glucose over time and the responses to behavioral interventions to reduce risk. This study performed longitudinal assessment of microRNAs and fasting blood glucose and identified relationships between microRNAs and behavioral risk reduction interventions. METHODS: MicroRNAs (n = 353) were measured in subsets (n = 10, n = 8) of participants from previously completed clinical trials that studied behavioral risk reduction interventions. Fasting blood glucose trajectories were associated with changes in 45 microRNAs over 12 months. RESULTS: Following a 3‐month physical activity and dietary intervention compared with baseline, 13 microRNAs were differentially expressed. Seven microRNAs (i.e. miR‐106b, miR‐20b, miR‐363, miR‐486, miR‐532, miR‐92a and miR‐93) were commonly identified between the two analyses. CONCLUSIONS: Further studies are needed to determine which microRNAs are prognostic biomarkers of risk for type 2 diabetes versus consequences of impaired glucose metabolism. Additional future directions of this research are to differentiate whether microRNAs are prognostic and/or diagnostic biomarkers for risk for type 2 diabetes and predictive biomarkers of responses to risk reduction interventions. John Wiley and Sons Inc. 2017-10-27 /pmc/articles/PMC5729496/ /pubmed/29259803 http://dx.doi.org/10.1002/osp4.134 Text en © 2017 The Authors. Obesity Science & Practice published by John Wiley & Sons Ltd, World Obesity and The Obesity Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Short Communications
Flowers, E.
Kanaya, A. M.
Fukuoka, Y.
Allen, I. E.
Cooper, B.
Aouizerat, B. E.
Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title_full Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title_fullStr Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title_full_unstemmed Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title_short Preliminary evidence supports circulating microRNAs as prognostic biomarkers for type 2 diabetes
title_sort preliminary evidence supports circulating micrornas as prognostic biomarkers for type 2 diabetes
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729496/
https://www.ncbi.nlm.nih.gov/pubmed/29259803
http://dx.doi.org/10.1002/osp4.134
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