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Circulating miR-216a as a biomarker of metabolic alterations and obesity in women
Obesity leads to an amplified risk of disease and contributes to the occurrence of type 2 diabetes, fatty liver disease, coronary heart disease, stroke, chronic kidney disease and various types of cancer. MicroRNAs (miRNAs), small non-coding RNA molecules of 20–25 nucleotides, can remain stable in p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479169/ https://www.ncbi.nlm.nih.gov/pubmed/32954093 http://dx.doi.org/10.1016/j.ncrna.2020.08.001 |
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author | Vonhögen, Indira G.C. Mohseni, Zenab Winkens, Bjorn Xiao, Ke Thum, Thomas Calore, Martina da Costa Martins, Paula A. de Windt, Leon J. Spaanderman, Marc E.A. Ghossein-Doha, Chahinda |
author_facet | Vonhögen, Indira G.C. Mohseni, Zenab Winkens, Bjorn Xiao, Ke Thum, Thomas Calore, Martina da Costa Martins, Paula A. de Windt, Leon J. Spaanderman, Marc E.A. Ghossein-Doha, Chahinda |
author_sort | Vonhögen, Indira G.C. |
collection | PubMed |
description | Obesity leads to an amplified risk of disease and contributes to the occurrence of type 2 diabetes, fatty liver disease, coronary heart disease, stroke, chronic kidney disease and various types of cancer. MicroRNAs (miRNAs), small non-coding RNA molecules of 20–25 nucleotides, can remain stable in plasma and have been studied as potential (predictive) biomarkers for obesity and related metabolic disorders. The aim of this study was to identify circulating miRNAs as biomarkers for obesity status and metabolic alterations in women. Circulating miR-216a and miR-155–5p were selected by miRNA expression profiling and validated by real time quantitative PCR in a validation cohort of 60 obese women and 60 normal weight-age-matched control women. This was supplemented by correlation analysis of the candidate miRNA and anthropometric variables, blood biochemistry and lipid profile markers. Circulating miR-216a was validated as a biomarker of obesity status with significantly reduced levels in obese women. Interestingly, this was associated with a negative correlation between the plasma miR-216a content and body mass index (BMI), waist circumference, mean arterial pressure (MAP), triglycerides, ratio of total cholesterol/high density lipoprotein (HDL)-cholesterol and high sensitivity-C reactive protein (hs-CRP).Taken together, we provide evidence for an abnormally expressed circulating miRNA, miR-216a, with additive value as a predictive marker for obesity that correlates with metabolic alterations presented by lipid profile and inflammatory markers. |
format | Online Article Text |
id | pubmed-7479169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-74791692020-09-17 Circulating miR-216a as a biomarker of metabolic alterations and obesity in women Vonhögen, Indira G.C. Mohseni, Zenab Winkens, Bjorn Xiao, Ke Thum, Thomas Calore, Martina da Costa Martins, Paula A. de Windt, Leon J. Spaanderman, Marc E.A. Ghossein-Doha, Chahinda Noncoding RNA Res Article Obesity leads to an amplified risk of disease and contributes to the occurrence of type 2 diabetes, fatty liver disease, coronary heart disease, stroke, chronic kidney disease and various types of cancer. MicroRNAs (miRNAs), small non-coding RNA molecules of 20–25 nucleotides, can remain stable in plasma and have been studied as potential (predictive) biomarkers for obesity and related metabolic disorders. The aim of this study was to identify circulating miRNAs as biomarkers for obesity status and metabolic alterations in women. Circulating miR-216a and miR-155–5p were selected by miRNA expression profiling and validated by real time quantitative PCR in a validation cohort of 60 obese women and 60 normal weight-age-matched control women. This was supplemented by correlation analysis of the candidate miRNA and anthropometric variables, blood biochemistry and lipid profile markers. Circulating miR-216a was validated as a biomarker of obesity status with significantly reduced levels in obese women. Interestingly, this was associated with a negative correlation between the plasma miR-216a content and body mass index (BMI), waist circumference, mean arterial pressure (MAP), triglycerides, ratio of total cholesterol/high density lipoprotein (HDL)-cholesterol and high sensitivity-C reactive protein (hs-CRP).Taken together, we provide evidence for an abnormally expressed circulating miRNA, miR-216a, with additive value as a predictive marker for obesity that correlates with metabolic alterations presented by lipid profile and inflammatory markers. KeAi Publishing 2020-08-22 /pmc/articles/PMC7479169/ /pubmed/32954093 http://dx.doi.org/10.1016/j.ncrna.2020.08.001 Text en © 2020 [The Author/The Authors] http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Vonhögen, Indira G.C. Mohseni, Zenab Winkens, Bjorn Xiao, Ke Thum, Thomas Calore, Martina da Costa Martins, Paula A. de Windt, Leon J. Spaanderman, Marc E.A. Ghossein-Doha, Chahinda Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title | Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title_full | Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title_fullStr | Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title_full_unstemmed | Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title_short | Circulating miR-216a as a biomarker of metabolic alterations and obesity in women |
title_sort | circulating mir-216a as a biomarker of metabolic alterations and obesity in women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479169/ https://www.ncbi.nlm.nih.gov/pubmed/32954093 http://dx.doi.org/10.1016/j.ncrna.2020.08.001 |
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