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Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome

BACKGROUND: Adiponectin acts as an antidiabetic, antiinflammatory and antiatherogenic adipokine. These effects are assumed to be mediated by the recently discovered adiponectin receptors AdipoR1 and AdipoR2. AIM: The purpose of this study was to determine whether variations in the AdipoR1 and AdipoR...

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Autores principales: Broedl, Uli C, Lehrke, Michael, Fleischer-Brielmaier, Elisabeth, Tietz, Anne B, Nagel, Jutta M, Göke, Burkhard, Lohse, Peter, Parhofer, Klaus G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1482678/
https://www.ncbi.nlm.nih.gov/pubmed/16700915
http://dx.doi.org/10.1186/1475-2840-5-11
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author Broedl, Uli C
Lehrke, Michael
Fleischer-Brielmaier, Elisabeth
Tietz, Anne B
Nagel, Jutta M
Göke, Burkhard
Lohse, Peter
Parhofer, Klaus G
author_facet Broedl, Uli C
Lehrke, Michael
Fleischer-Brielmaier, Elisabeth
Tietz, Anne B
Nagel, Jutta M
Göke, Burkhard
Lohse, Peter
Parhofer, Klaus G
author_sort Broedl, Uli C
collection PubMed
description BACKGROUND: Adiponectin acts as an antidiabetic, antiinflammatory and antiatherogenic adipokine. These effects are assumed to be mediated by the recently discovered adiponectin receptors AdipoR1 and AdipoR2. AIM: The purpose of this study was to determine whether variations in the AdipoR1 and AdipoR2 genes may contribute to insulin resistance, dyslipidemia and inflammation. METHODS: We sequenced all seven coding exons of both genes in 20 unrelated German subjects with metabolic syndrome and tested genetic variants for association with glucose, lipid and inflammatory parameters. RESULTS: We identified three AdipoR2 variants (+795G/A, +870C/A and +963C/T) in perfect linkage disequilibrium (r(2 )= 1) with a minor allele frequency of 0.125. This haplotype was associated with higher plasma adiponectin levels and decreased fasting triglyceride, VLDL-triglyceride and VLDL-cholesterol levels. No association, however, was observed between the AdipoR2 SNP cluster and glucose metabolism. CONCLUSION: To our knowledge, this is the first study to identify an association between genetic variants of the adiponectin receptor genes and plasma adiponectin levels. Furthermore, our data suggest that AdipoR2 may play an important role in triglyceride/VLDL metabolism.
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spelling pubmed-14826782006-06-24 Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome Broedl, Uli C Lehrke, Michael Fleischer-Brielmaier, Elisabeth Tietz, Anne B Nagel, Jutta M Göke, Burkhard Lohse, Peter Parhofer, Klaus G Cardiovasc Diabetol Original Investigation BACKGROUND: Adiponectin acts as an antidiabetic, antiinflammatory and antiatherogenic adipokine. These effects are assumed to be mediated by the recently discovered adiponectin receptors AdipoR1 and AdipoR2. AIM: The purpose of this study was to determine whether variations in the AdipoR1 and AdipoR2 genes may contribute to insulin resistance, dyslipidemia and inflammation. METHODS: We sequenced all seven coding exons of both genes in 20 unrelated German subjects with metabolic syndrome and tested genetic variants for association with glucose, lipid and inflammatory parameters. RESULTS: We identified three AdipoR2 variants (+795G/A, +870C/A and +963C/T) in perfect linkage disequilibrium (r(2 )= 1) with a minor allele frequency of 0.125. This haplotype was associated with higher plasma adiponectin levels and decreased fasting triglyceride, VLDL-triglyceride and VLDL-cholesterol levels. No association, however, was observed between the AdipoR2 SNP cluster and glucose metabolism. CONCLUSION: To our knowledge, this is the first study to identify an association between genetic variants of the adiponectin receptor genes and plasma adiponectin levels. Furthermore, our data suggest that AdipoR2 may play an important role in triglyceride/VLDL metabolism. BioMed Central 2006-05-15 /pmc/articles/PMC1482678/ /pubmed/16700915 http://dx.doi.org/10.1186/1475-2840-5-11 Text en Copyright © 2006 Broedl 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 Original Investigation
Broedl, Uli C
Lehrke, Michael
Fleischer-Brielmaier, Elisabeth
Tietz, Anne B
Nagel, Jutta M
Göke, Burkhard
Lohse, Peter
Parhofer, Klaus G
Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title_full Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title_fullStr Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title_full_unstemmed Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title_short Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome
title_sort genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/vldl levels in patients with metabolic syndrome
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1482678/
https://www.ncbi.nlm.nih.gov/pubmed/16700915
http://dx.doi.org/10.1186/1475-2840-5-11
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