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The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients
Polycystic ovary syndrome (PCOS) is a disorder characterized by hyperandrogenism, oligo- or anovulation, and/or polycystic ovary. It frequently presents with dyslipidemia and insulin resistance. Recent studies have shown that the white adipose tissue-derived asprosin is elevated in humans with insul...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558936/ https://www.ncbi.nlm.nih.gov/pubmed/31015585 http://dx.doi.org/10.1038/s41598-019-42061-9 |
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author | Chang, Chia Lin Huang, Shang Yu Hsu, Ya Chiung Chin, Tzu Hsuan Soong, Yung Kuei |
author_facet | Chang, Chia Lin Huang, Shang Yu Hsu, Ya Chiung Chin, Tzu Hsuan Soong, Yung Kuei |
author_sort | Chang, Chia Lin |
collection | PubMed |
description | Polycystic ovary syndrome (PCOS) is a disorder characterized by hyperandrogenism, oligo- or anovulation, and/or polycystic ovary. It frequently presents with dyslipidemia and insulin resistance. Recent studies have shown that the white adipose tissue-derived asprosin is elevated in humans with insulin resistance. Because many PCOS patients have a propensity to develop dyslipidemia and/or insulin resistance, asprosin metabolism could be dysregulated in PCOS patients. Accordingly, we investigated serum levels of asprosin, irisin, GIP, androgens, LH, glucose, insulin, and lipids as well as HOMA-IR, QUICKI and ISI (Matsuda) in a cohort of 444 PCOS patients and 156 controls. Patients were stratified based on metabolic syndrome risk factors (ATPIII [+] and [−] groups), or BMI (overweight and lean groups). The irisin level was significantly correlated with body weight, SBP, DBP, Ferriman–Gallwey score, and levels of TSH, triglycerides, glucose and insulin in the overall population, and was elevated in ATPIII(+) and overweight PCOS patients compared to corresponding controls. By contrast, asprosin levels in PCOS, ATPIII(+), or overweight patients were similar to those of corresponding controls. This finding indicated that the regulation of irisin, but not asprosin, metabolism is abnormal in PCOS patients, and this metabolic characteristic is distinctly different from that of diabetes patients. |
format | Online Article Text |
id | pubmed-6558936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65589362019-06-19 The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients Chang, Chia Lin Huang, Shang Yu Hsu, Ya Chiung Chin, Tzu Hsuan Soong, Yung Kuei Sci Rep Article Polycystic ovary syndrome (PCOS) is a disorder characterized by hyperandrogenism, oligo- or anovulation, and/or polycystic ovary. It frequently presents with dyslipidemia and insulin resistance. Recent studies have shown that the white adipose tissue-derived asprosin is elevated in humans with insulin resistance. Because many PCOS patients have a propensity to develop dyslipidemia and/or insulin resistance, asprosin metabolism could be dysregulated in PCOS patients. Accordingly, we investigated serum levels of asprosin, irisin, GIP, androgens, LH, glucose, insulin, and lipids as well as HOMA-IR, QUICKI and ISI (Matsuda) in a cohort of 444 PCOS patients and 156 controls. Patients were stratified based on metabolic syndrome risk factors (ATPIII [+] and [−] groups), or BMI (overweight and lean groups). The irisin level was significantly correlated with body weight, SBP, DBP, Ferriman–Gallwey score, and levels of TSH, triglycerides, glucose and insulin in the overall population, and was elevated in ATPIII(+) and overweight PCOS patients compared to corresponding controls. By contrast, asprosin levels in PCOS, ATPIII(+), or overweight patients were similar to those of corresponding controls. This finding indicated that the regulation of irisin, but not asprosin, metabolism is abnormal in PCOS patients, and this metabolic characteristic is distinctly different from that of diabetes patients. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6558936/ /pubmed/31015585 http://dx.doi.org/10.1038/s41598-019-42061-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chang, Chia Lin Huang, Shang Yu Hsu, Ya Chiung Chin, Tzu Hsuan Soong, Yung Kuei The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title | The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title_full | The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title_fullStr | The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title_full_unstemmed | The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title_short | The serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
title_sort | serum level of irisin, but not asprosin, is abnormal in polycystic ovary syndrome patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558936/ https://www.ncbi.nlm.nih.gov/pubmed/31015585 http://dx.doi.org/10.1038/s41598-019-42061-9 |
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