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Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients

OBJECTIVE: The insulin-like growth factors (IGFs) and their binding proteins (IGFBPs) are thought to play a significant role in metabolic pathways and glucose metabolism. Unregulated levels of IGFs/IGFBPs have been associated with the development of glucose intolerance and metabolic syndrome X (MSx)...

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Autores principales: Pouriamehr, Somayeh, Barmaki, Haleh, Rastegary, Mozhdeh, Lotfi, Farzaneh, Nabi Afjadi, Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788073/
https://www.ncbi.nlm.nih.gov/pubmed/31601230
http://dx.doi.org/10.1186/s13104-019-4492-9
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author Pouriamehr, Somayeh
Barmaki, Haleh
Rastegary, Mozhdeh
Lotfi, Farzaneh
Nabi Afjadi, Mohsen
author_facet Pouriamehr, Somayeh
Barmaki, Haleh
Rastegary, Mozhdeh
Lotfi, Farzaneh
Nabi Afjadi, Mohsen
author_sort Pouriamehr, Somayeh
collection PubMed
description OBJECTIVE: The insulin-like growth factors (IGFs) and their binding proteins (IGFBPs) are thought to play a significant role in metabolic pathways and glucose metabolism. Unregulated levels of IGFs/IGFBPs have been associated with the development of glucose intolerance and metabolic syndrome X (MSx). We hypothesized that change of IGFs/IGFBPs levels could increase the risk of MSx; thus, this study aimed to evaluate the serostatus of IGFs/IGFBPs in individuals with MSx. RESULTS: After adjustment for metabolic parameters, MSx patients had a lower level of IGF-1, IGFBP-1, and IGFBP-2 compared with subjects in the control group. Further analysis revealed a positive correlation between serum levels of IGF-1 and IGF-2 (p < 0.05), as well as serum IGFBP-3 and IGF-2 (p < 0.05). Also, the statistical analysis showed a negative association of serum IGF-1 with plasma glucose and total cholesterol levels (p < 0.05). Besides, a negative relationship was found between serum concentrations of IGF-1/IGF-2 and the risk of developing MSx. These data indicated that some components of IGFs/IGFBPs are linked with the pathogenesis of MSx. In conclusion, these inverse associations showed a possible linkage between the IGF/IGFBP signaling pathway and the development of MSx. It seems the decreased concentrations of IGFs edmay be regarded as a potential biomarker for early diagnosis or even prognosis of MSx but need more systematic studies to confirmed it.
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spelling pubmed-67880732019-10-18 Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients Pouriamehr, Somayeh Barmaki, Haleh Rastegary, Mozhdeh Lotfi, Farzaneh Nabi Afjadi, Mohsen BMC Res Notes Research Note OBJECTIVE: The insulin-like growth factors (IGFs) and their binding proteins (IGFBPs) are thought to play a significant role in metabolic pathways and glucose metabolism. Unregulated levels of IGFs/IGFBPs have been associated with the development of glucose intolerance and metabolic syndrome X (MSx). We hypothesized that change of IGFs/IGFBPs levels could increase the risk of MSx; thus, this study aimed to evaluate the serostatus of IGFs/IGFBPs in individuals with MSx. RESULTS: After adjustment for metabolic parameters, MSx patients had a lower level of IGF-1, IGFBP-1, and IGFBP-2 compared with subjects in the control group. Further analysis revealed a positive correlation between serum levels of IGF-1 and IGF-2 (p < 0.05), as well as serum IGFBP-3 and IGF-2 (p < 0.05). Also, the statistical analysis showed a negative association of serum IGF-1 with plasma glucose and total cholesterol levels (p < 0.05). Besides, a negative relationship was found between serum concentrations of IGF-1/IGF-2 and the risk of developing MSx. These data indicated that some components of IGFs/IGFBPs are linked with the pathogenesis of MSx. In conclusion, these inverse associations showed a possible linkage between the IGF/IGFBP signaling pathway and the development of MSx. It seems the decreased concentrations of IGFs edmay be regarded as a potential biomarker for early diagnosis or even prognosis of MSx but need more systematic studies to confirmed it. BioMed Central 2019-10-11 /pmc/articles/PMC6788073/ /pubmed/31601230 http://dx.doi.org/10.1186/s13104-019-4492-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Note
Pouriamehr, Somayeh
Barmaki, Haleh
Rastegary, Mozhdeh
Lotfi, Farzaneh
Nabi Afjadi, Mohsen
Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title_full Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title_fullStr Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title_full_unstemmed Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title_short Investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
title_sort investigation of insulin-like growth factors/insulin-like growth factor binding proteins regulation in metabolic syndrome patients
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6788073/
https://www.ncbi.nlm.nih.gov/pubmed/31601230
http://dx.doi.org/10.1186/s13104-019-4492-9
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