Cargando…

Circulating microRNAs have a sex-specific association with metabolic syndrome

BACKGROUND: The microRNAs let-7 g and miR-221 have been demonstrated to be related to the glucose metabolism. This study assessed the serum levels of these two microRNAs in subjects with and without metabolic syndrome (MetS). RESULTS: The serum microRNA levels were detected in 102 subjects aged 40 t...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yu-Ting, Tsai, Pei-Chien, Liao, Yi-Chu, Hsu, Chung-Y, Juo, Suh-Hang Hank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851553/
https://www.ncbi.nlm.nih.gov/pubmed/24093444
http://dx.doi.org/10.1186/1423-0127-20-72
_version_ 1782294304144752640
author Wang, Yu-Ting
Tsai, Pei-Chien
Liao, Yi-Chu
Hsu, Chung-Y
Juo, Suh-Hang Hank
author_facet Wang, Yu-Ting
Tsai, Pei-Chien
Liao, Yi-Chu
Hsu, Chung-Y
Juo, Suh-Hang Hank
author_sort Wang, Yu-Ting
collection PubMed
description BACKGROUND: The microRNAs let-7 g and miR-221 have been demonstrated to be related to the glucose metabolism. This study assessed the serum levels of these two microRNAs in subjects with and without metabolic syndrome (MetS). RESULTS: The serum microRNA levels were detected in 102 subjects aged 40 to 80 years who were recruited from the general population. The status of MetS was defined by the Adult Treatment Panel III (ATP III) criteria modified for Asians. Subjects with histories of cardiovascular diseases or who were receiving treatment with hypoglycemic or lipid-lowering agents were excluded. The levels of both circulating microRNAs (let-7 g and miR-221) were higher in subjects with MetS (p = 0.004 and p = 0.01, respectively). The sex-specific analysis showed that the difference was more prominent in women (for both miRNAs, p < 0.05 in women and p > 0.1 in men). In the female subjects, increased expression of both microRNAs was associated with an increased number of MetS risk components (p = 0.002 for let-7 g and p = 0.022 for miR-221). Moreover, the elevation of serum let-7 g was significantly associated with a low level of high-density lipoprotein cholesterol (p = 0.022) and high blood pressure (p = 0.023). In contrast, the miR-221 level was not associated with any individual MetS risk component. CONCLUSIONS: The circulating levels of let-7 g and miR-221 displayed a female-specific elevation in individuals with metabolic syndrome.
format Online
Article
Text
id pubmed-3851553
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-38515532013-12-06 Circulating microRNAs have a sex-specific association with metabolic syndrome Wang, Yu-Ting Tsai, Pei-Chien Liao, Yi-Chu Hsu, Chung-Y Juo, Suh-Hang Hank J Biomed Sci Research BACKGROUND: The microRNAs let-7 g and miR-221 have been demonstrated to be related to the glucose metabolism. This study assessed the serum levels of these two microRNAs in subjects with and without metabolic syndrome (MetS). RESULTS: The serum microRNA levels were detected in 102 subjects aged 40 to 80 years who were recruited from the general population. The status of MetS was defined by the Adult Treatment Panel III (ATP III) criteria modified for Asians. Subjects with histories of cardiovascular diseases or who were receiving treatment with hypoglycemic or lipid-lowering agents were excluded. The levels of both circulating microRNAs (let-7 g and miR-221) were higher in subjects with MetS (p = 0.004 and p = 0.01, respectively). The sex-specific analysis showed that the difference was more prominent in women (for both miRNAs, p < 0.05 in women and p > 0.1 in men). In the female subjects, increased expression of both microRNAs was associated with an increased number of MetS risk components (p = 0.002 for let-7 g and p = 0.022 for miR-221). Moreover, the elevation of serum let-7 g was significantly associated with a low level of high-density lipoprotein cholesterol (p = 0.022) and high blood pressure (p = 0.023). In contrast, the miR-221 level was not associated with any individual MetS risk component. CONCLUSIONS: The circulating levels of let-7 g and miR-221 displayed a female-specific elevation in individuals with metabolic syndrome. BioMed Central 2013-10-04 /pmc/articles/PMC3851553/ /pubmed/24093444 http://dx.doi.org/10.1186/1423-0127-20-72 Text en Copyright © 2013 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wang, Yu-Ting
Tsai, Pei-Chien
Liao, Yi-Chu
Hsu, Chung-Y
Juo, Suh-Hang Hank
Circulating microRNAs have a sex-specific association with metabolic syndrome
title Circulating microRNAs have a sex-specific association with metabolic syndrome
title_full Circulating microRNAs have a sex-specific association with metabolic syndrome
title_fullStr Circulating microRNAs have a sex-specific association with metabolic syndrome
title_full_unstemmed Circulating microRNAs have a sex-specific association with metabolic syndrome
title_short Circulating microRNAs have a sex-specific association with metabolic syndrome
title_sort circulating micrornas have a sex-specific association with metabolic syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851553/
https://www.ncbi.nlm.nih.gov/pubmed/24093444
http://dx.doi.org/10.1186/1423-0127-20-72
work_keys_str_mv AT wangyuting circulatingmicrornashaveasexspecificassociationwithmetabolicsyndrome
AT tsaipeichien circulatingmicrornashaveasexspecificassociationwithmetabolicsyndrome
AT liaoyichu circulatingmicrornashaveasexspecificassociationwithmetabolicsyndrome
AT hsuchungy circulatingmicrornashaveasexspecificassociationwithmetabolicsyndrome
AT juosuhhanghank circulatingmicrornashaveasexspecificassociationwithmetabolicsyndrome