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Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity

PURPOSE: MicroRNAs (miRNAs) are implicated in metabolic changes accompanying progression of obesity, insulin resistance (IR), and metabolic disorders in children. Identifying circulating miRNAs that uniquely associate with these disorders may be useful in early identification and prevention of obesi...

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Autores principales: Lin, Haixia, Tas, Emir, Børsheim, Elisabet, Mercer, Kelly E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735788/
https://www.ncbi.nlm.nih.gov/pubmed/33328751
http://dx.doi.org/10.2147/DMSO.S273908
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author Lin, Haixia
Tas, Emir
Børsheim, Elisabet
Mercer, Kelly E
author_facet Lin, Haixia
Tas, Emir
Børsheim, Elisabet
Mercer, Kelly E
author_sort Lin, Haixia
collection PubMed
description PURPOSE: MicroRNAs (miRNAs) are implicated in metabolic changes accompanying progression of obesity, insulin resistance (IR), and metabolic disorders in children. Identifying circulating miRNAs that uniquely associate with these disorders may be useful in early identification and prevention of obesity-related complications. We aimed to identify circulating miRNA signatures that distinguish adolescents with obesity and IR from those with obesity unaccompanied by IR. METHODS: Adolescents (aged 10–17 years) with obesity were recruited from a weight management clinic. Fasting serum samples were obtained from 33 participants. A total of 179 miRNAs were queried by a quantitative RT-PCR-based miRNA focus panel. Differentially expressed miRNAs were compared between groups using Student’s t-test or one-way ANOVA analysis, and the association between IR evaluated by homeostatic model assessment model (HOMA-IR > 4) and body mass index (BMI) status was assessed using Pearson’s correlation analysis. RESULTS: We found an expression pattern consisting of 12 elevated miRNAs linked to IR in obese adolescents. miR-30d, -221, and -122 were significantly correlated with clinical and biochemical markers of obesity and IR, suggestive of IR in adolescents at risk. CONCLUSION: Specific signatures of circulating miRNAs reflected metabolic phenotypes and predicted the presence of IR in adolescents with obesity, suggesting that miRNA indicators may identify obesity-associated complications in childhood. Further studies will be needed to understand cause versus effect and the mechanisms by which IR status links to changes in blood miRNA profiles.
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spelling pubmed-77357882020-12-15 Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity Lin, Haixia Tas, Emir Børsheim, Elisabet Mercer, Kelly E Diabetes Metab Syndr Obes Original Research PURPOSE: MicroRNAs (miRNAs) are implicated in metabolic changes accompanying progression of obesity, insulin resistance (IR), and metabolic disorders in children. Identifying circulating miRNAs that uniquely associate with these disorders may be useful in early identification and prevention of obesity-related complications. We aimed to identify circulating miRNA signatures that distinguish adolescents with obesity and IR from those with obesity unaccompanied by IR. METHODS: Adolescents (aged 10–17 years) with obesity were recruited from a weight management clinic. Fasting serum samples were obtained from 33 participants. A total of 179 miRNAs were queried by a quantitative RT-PCR-based miRNA focus panel. Differentially expressed miRNAs were compared between groups using Student’s t-test or one-way ANOVA analysis, and the association between IR evaluated by homeostatic model assessment model (HOMA-IR > 4) and body mass index (BMI) status was assessed using Pearson’s correlation analysis. RESULTS: We found an expression pattern consisting of 12 elevated miRNAs linked to IR in obese adolescents. miR-30d, -221, and -122 were significantly correlated with clinical and biochemical markers of obesity and IR, suggestive of IR in adolescents at risk. CONCLUSION: Specific signatures of circulating miRNAs reflected metabolic phenotypes and predicted the presence of IR in adolescents with obesity, suggesting that miRNA indicators may identify obesity-associated complications in childhood. Further studies will be needed to understand cause versus effect and the mechanisms by which IR status links to changes in blood miRNA profiles. Dove 2020-12-10 /pmc/articles/PMC7735788/ /pubmed/33328751 http://dx.doi.org/10.2147/DMSO.S273908 Text en © 2020 Lin et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Lin, Haixia
Tas, Emir
Børsheim, Elisabet
Mercer, Kelly E
Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title_full Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title_fullStr Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title_full_unstemmed Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title_short Circulating miRNA Signatures Associated with Insulin Resistance in Adolescents with Obesity
title_sort circulating mirna signatures associated with insulin resistance in adolescents with obesity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735788/
https://www.ncbi.nlm.nih.gov/pubmed/33328751
http://dx.doi.org/10.2147/DMSO.S273908
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