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Effect of diabetes on exosomal miRNA profile in patients with obesity
INTRODUCTION: Obesity is a risk factor for type 2 diabetes mellitus (T2DM) and cardiovascular disease. T2DM increases the risk of cardiovascular-related death. We investigated changes in circulating exosomal microRNA (miRNA) profiles in patients with DM with obesity compared with patients without DM...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473624/ https://www.ncbi.nlm.nih.gov/pubmed/32883688 http://dx.doi.org/10.1136/bmjdrc-2020-001403 |
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author | Kim, Hyoshik Bae, Yun-Ui Lee, Haekyung Kim, Hyoungnae Jeon, Jin Seok Noh, Hyunjin Han, Dong Cheol Byun, Dong Won Kim, Sang Hyun Park, Hyeong Kyu Ryu, Seongho Kwon, Soon Hyo |
author_facet | Kim, Hyoshik Bae, Yun-Ui Lee, Haekyung Kim, Hyoungnae Jeon, Jin Seok Noh, Hyunjin Han, Dong Cheol Byun, Dong Won Kim, Sang Hyun Park, Hyeong Kyu Ryu, Seongho Kwon, Soon Hyo |
author_sort | Kim, Hyoshik |
collection | PubMed |
description | INTRODUCTION: Obesity is a risk factor for type 2 diabetes mellitus (T2DM) and cardiovascular disease. T2DM increases the risk of cardiovascular-related death. We investigated changes in circulating exosomal microRNA (miRNA) profiles in patients with DM with obesity compared with patients without DM with obesity. RESEARCH DESIGN AND METHODS: This prospective study involved 29 patients with obesity (patients without DM=16, patients with DM=13) and healthy volunteers (HVs) (n=18). We measured circulating levels of exosomal miRNAs by next-generation sequencing and compared miRNA levels across the three groups. RESULTS: The expression levels of 25 miRNAs (upregulated=14, downregulated=11) differed between patients with obesity with DM and patients with obesity without DM. Compared with HV, patients with DM with obesity had 53 dysregulated miRNAs. Additionally, moving stepwise from HV to patients with obesity without DM to patients with obesity with DM, there was a consistent increase in expression levels of miR-23a-5p and miR-6087 and a consistent decrease in expressions levels of miR-6751-3p. CONCLUSIONS: Our data show that the exosomal miRNAs is altered by dysregulated glucose metabolism in patients with obesity. This circulating exosomal miRNA signature in patients with obesity with or without DM is a potential biomarker and therapeutic target in these patients. |
format | Online Article Text |
id | pubmed-7473624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-74736242020-09-16 Effect of diabetes on exosomal miRNA profile in patients with obesity Kim, Hyoshik Bae, Yun-Ui Lee, Haekyung Kim, Hyoungnae Jeon, Jin Seok Noh, Hyunjin Han, Dong Cheol Byun, Dong Won Kim, Sang Hyun Park, Hyeong Kyu Ryu, Seongho Kwon, Soon Hyo BMJ Open Diabetes Res Care Obesity Studies INTRODUCTION: Obesity is a risk factor for type 2 diabetes mellitus (T2DM) and cardiovascular disease. T2DM increases the risk of cardiovascular-related death. We investigated changes in circulating exosomal microRNA (miRNA) profiles in patients with DM with obesity compared with patients without DM with obesity. RESEARCH DESIGN AND METHODS: This prospective study involved 29 patients with obesity (patients without DM=16, patients with DM=13) and healthy volunteers (HVs) (n=18). We measured circulating levels of exosomal miRNAs by next-generation sequencing and compared miRNA levels across the three groups. RESULTS: The expression levels of 25 miRNAs (upregulated=14, downregulated=11) differed between patients with obesity with DM and patients with obesity without DM. Compared with HV, patients with DM with obesity had 53 dysregulated miRNAs. Additionally, moving stepwise from HV to patients with obesity without DM to patients with obesity with DM, there was a consistent increase in expression levels of miR-23a-5p and miR-6087 and a consistent decrease in expressions levels of miR-6751-3p. CONCLUSIONS: Our data show that the exosomal miRNAs is altered by dysregulated glucose metabolism in patients with obesity. This circulating exosomal miRNA signature in patients with obesity with or without DM is a potential biomarker and therapeutic target in these patients. BMJ Publishing Group 2020-09-03 /pmc/articles/PMC7473624/ /pubmed/32883688 http://dx.doi.org/10.1136/bmjdrc-2020-001403 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Obesity Studies Kim, Hyoshik Bae, Yun-Ui Lee, Haekyung Kim, Hyoungnae Jeon, Jin Seok Noh, Hyunjin Han, Dong Cheol Byun, Dong Won Kim, Sang Hyun Park, Hyeong Kyu Ryu, Seongho Kwon, Soon Hyo Effect of diabetes on exosomal miRNA profile in patients with obesity |
title | Effect of diabetes on exosomal miRNA profile in patients with obesity |
title_full | Effect of diabetes on exosomal miRNA profile in patients with obesity |
title_fullStr | Effect of diabetes on exosomal miRNA profile in patients with obesity |
title_full_unstemmed | Effect of diabetes on exosomal miRNA profile in patients with obesity |
title_short | Effect of diabetes on exosomal miRNA profile in patients with obesity |
title_sort | effect of diabetes on exosomal mirna profile in patients with obesity |
topic | Obesity Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473624/ https://www.ncbi.nlm.nih.gov/pubmed/32883688 http://dx.doi.org/10.1136/bmjdrc-2020-001403 |
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