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Circulating and Exosomal microRNA-33 in Childhood Obesity

Background: MicroRNA-33 may control a wide range of different metabolic functions. Methods: This study aims to assess the miR-33a circulating profile in normal-weight (N = 20) and obese (O = 30) adolescents and to correlate its expression levels to their metabolic parameters. In a subset of subjects...

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Autores principales: Cabiati, Manuela, Guiducci, Letizia, Randazzo, Emioli, Casieri, Valentina, Federico, Giovanni, Del Ry, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452681/
https://www.ncbi.nlm.nih.gov/pubmed/37626791
http://dx.doi.org/10.3390/biomedicines11082295
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author Cabiati, Manuela
Guiducci, Letizia
Randazzo, Emioli
Casieri, Valentina
Federico, Giovanni
Del Ry, Silvia
author_facet Cabiati, Manuela
Guiducci, Letizia
Randazzo, Emioli
Casieri, Valentina
Federico, Giovanni
Del Ry, Silvia
author_sort Cabiati, Manuela
collection PubMed
description Background: MicroRNA-33 may control a wide range of different metabolic functions. Methods: This study aims to assess the miR-33a circulating profile in normal-weight (N = 20) and obese (O = 30) adolescents and to correlate its expression levels to their metabolic parameters. In a subset of subjects, we compared circulating miR-33a with exosomal miR-33a. Results: Metabolic parameters were altered in O, with initial hyperinsulinemia. Circulating miR-33a was significantly higher in O than in N (p = 0.0002). Significant correlations between miR-33a and auxological and metabolic indices (Insulin p = 0.01; Cholesterol p = 0.01; LDL p = 0.01; HbA1c p = 0.01) were found. Splitting our population (O + N) into two groups, according to the median value of mRNA expression miR-33a levels (0.701), irrespective of the presence or absence of obesity, we observed that those having a higher expression of miR-33a were more frequently obese (87.5% vs. 12.5%; p < 0.0001) and had significantly increased values of auxological and metabolic parameters. Exosomes extracted from plasma of N and O carried miR-33a, and its expression was lower in O (p = 0.026). No correlations with metabolic parameters were observed. Conclusion: While exosome miR-33a does not provide any advantage, circulating miR-33a can provide important indications in an initial phase of metabolic dysfunction, stratifying obese adolescents at higher cardiometabolic risk.
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spelling pubmed-104526812023-08-26 Circulating and Exosomal microRNA-33 in Childhood Obesity Cabiati, Manuela Guiducci, Letizia Randazzo, Emioli Casieri, Valentina Federico, Giovanni Del Ry, Silvia Biomedicines Article Background: MicroRNA-33 may control a wide range of different metabolic functions. Methods: This study aims to assess the miR-33a circulating profile in normal-weight (N = 20) and obese (O = 30) adolescents and to correlate its expression levels to their metabolic parameters. In a subset of subjects, we compared circulating miR-33a with exosomal miR-33a. Results: Metabolic parameters were altered in O, with initial hyperinsulinemia. Circulating miR-33a was significantly higher in O than in N (p = 0.0002). Significant correlations between miR-33a and auxological and metabolic indices (Insulin p = 0.01; Cholesterol p = 0.01; LDL p = 0.01; HbA1c p = 0.01) were found. Splitting our population (O + N) into two groups, according to the median value of mRNA expression miR-33a levels (0.701), irrespective of the presence or absence of obesity, we observed that those having a higher expression of miR-33a were more frequently obese (87.5% vs. 12.5%; p < 0.0001) and had significantly increased values of auxological and metabolic parameters. Exosomes extracted from plasma of N and O carried miR-33a, and its expression was lower in O (p = 0.026). No correlations with metabolic parameters were observed. Conclusion: While exosome miR-33a does not provide any advantage, circulating miR-33a can provide important indications in an initial phase of metabolic dysfunction, stratifying obese adolescents at higher cardiometabolic risk. MDPI 2023-08-18 /pmc/articles/PMC10452681/ /pubmed/37626791 http://dx.doi.org/10.3390/biomedicines11082295 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cabiati, Manuela
Guiducci, Letizia
Randazzo, Emioli
Casieri, Valentina
Federico, Giovanni
Del Ry, Silvia
Circulating and Exosomal microRNA-33 in Childhood Obesity
title Circulating and Exosomal microRNA-33 in Childhood Obesity
title_full Circulating and Exosomal microRNA-33 in Childhood Obesity
title_fullStr Circulating and Exosomal microRNA-33 in Childhood Obesity
title_full_unstemmed Circulating and Exosomal microRNA-33 in Childhood Obesity
title_short Circulating and Exosomal microRNA-33 in Childhood Obesity
title_sort circulating and exosomal microrna-33 in childhood obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452681/
https://www.ncbi.nlm.nih.gov/pubmed/37626791
http://dx.doi.org/10.3390/biomedicines11082295
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