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Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance

Our objective is to determine circulating Bone morphogenetic protein-9(BMP-9) levels in subjects with Metabolic Syndrome (MetS) and examine the relationship between BMP-9 and conventional markers for MetS and insulin resistance (IR). A total of 362 newly diagnosed patients with MetS along with healt...

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Autores principales: Xu, Xiaohui, Li, Xiaoqiang, Yang, Gangyi, Li, Ling, Hu, Wenjing, Zhang, Lili, Liu, Hua, Zheng, Hongting, Tan, Minghong, Zhu, Danping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727514/
https://www.ncbi.nlm.nih.gov/pubmed/29235531
http://dx.doi.org/10.1038/s41598-017-17807-y
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author Xu, Xiaohui
Li, Xiaoqiang
Yang, Gangyi
Li, Ling
Hu, Wenjing
Zhang, Lili
Liu, Hua
Zheng, Hongting
Tan, Minghong
Zhu, Danping
author_facet Xu, Xiaohui
Li, Xiaoqiang
Yang, Gangyi
Li, Ling
Hu, Wenjing
Zhang, Lili
Liu, Hua
Zheng, Hongting
Tan, Minghong
Zhu, Danping
author_sort Xu, Xiaohui
collection PubMed
description Our objective is to determine circulating Bone morphogenetic protein-9(BMP-9) levels in subjects with Metabolic Syndrome (MetS) and examine the relationship between BMP-9 and conventional markers for MetS and insulin resistance (IR). A total of 362 newly diagnosed patients with MetS along with healthy controls were recruited for this cross-sectional study. Circulating BMP-9 levels were measured by ELISA. Circulating BMP-9 levels were significantly lower in MetS patients compared to those of the healthy controls. BMP-9 was associated negatively with Waist hip ratio (WHR), fasting blood glucose (FBG), 2-hour blood glucose after glucose overload (2h-OGTT), HbA1c, triglyceride (TG) levels and HOMA-IR and positively with free fatty acid (FFA) and HDL after control for age and sex. In a multiple linear regression, BMP-9 was independently associated with type 2 diabetes mellitus (T2DM), HOMA-IR and FFA. Binary logistic regression showed that plasma BMP-9 concentrations were significantly associated with MetS even after controlling for anthropometric variables and lipid profiles. In addition, circulating BMP-9 levels reduced progressively with an increasing number of MetS components. The best cutoff values for circulating BMP-9 to predict MetS was 56.6 ng/L. Circulating BMP-9 levels were associated with the key components of MetS and IR.
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spelling pubmed-57275142017-12-18 Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance Xu, Xiaohui Li, Xiaoqiang Yang, Gangyi Li, Ling Hu, Wenjing Zhang, Lili Liu, Hua Zheng, Hongting Tan, Minghong Zhu, Danping Sci Rep Article Our objective is to determine circulating Bone morphogenetic protein-9(BMP-9) levels in subjects with Metabolic Syndrome (MetS) and examine the relationship between BMP-9 and conventional markers for MetS and insulin resistance (IR). A total of 362 newly diagnosed patients with MetS along with healthy controls were recruited for this cross-sectional study. Circulating BMP-9 levels were measured by ELISA. Circulating BMP-9 levels were significantly lower in MetS patients compared to those of the healthy controls. BMP-9 was associated negatively with Waist hip ratio (WHR), fasting blood glucose (FBG), 2-hour blood glucose after glucose overload (2h-OGTT), HbA1c, triglyceride (TG) levels and HOMA-IR and positively with free fatty acid (FFA) and HDL after control for age and sex. In a multiple linear regression, BMP-9 was independently associated with type 2 diabetes mellitus (T2DM), HOMA-IR and FFA. Binary logistic regression showed that plasma BMP-9 concentrations were significantly associated with MetS even after controlling for anthropometric variables and lipid profiles. In addition, circulating BMP-9 levels reduced progressively with an increasing number of MetS components. The best cutoff values for circulating BMP-9 to predict MetS was 56.6 ng/L. Circulating BMP-9 levels were associated with the key components of MetS and IR. Nature Publishing Group UK 2017-12-13 /pmc/articles/PMC5727514/ /pubmed/29235531 http://dx.doi.org/10.1038/s41598-017-17807-y Text en © The Author(s) 2017 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
Xu, Xiaohui
Li, Xiaoqiang
Yang, Gangyi
Li, Ling
Hu, Wenjing
Zhang, Lili
Liu, Hua
Zheng, Hongting
Tan, Minghong
Zhu, Danping
Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title_full Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title_fullStr Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title_full_unstemmed Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title_short Circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
title_sort circulating bone morphogenetic protein-9 in relation to metabolic syndrome and insulin resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727514/
https://www.ncbi.nlm.nih.gov/pubmed/29235531
http://dx.doi.org/10.1038/s41598-017-17807-y
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