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Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais

BACKGROUND: Metabolic syndrome (MS) is a clinical constellation comprising risk factors associated with developing cardiovascular disease and type 2 diabetes. Resistin has been suggested as a linkage between obesity, inflammation and type 2 diabetes. This study aimed to investigate resistin concentr...

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Autores principales: Suriyaprom, Kanjana, Tungtrongchitr, Rungsunn, Namjuntra, Pisit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Medical Biochemists of Serbia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922327/
https://www.ncbi.nlm.nih.gov/pubmed/28356829
http://dx.doi.org/10.2478/jomb-2014-0034
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author Suriyaprom, Kanjana
Tungtrongchitr, Rungsunn
Namjuntra, Pisit
author_facet Suriyaprom, Kanjana
Tungtrongchitr, Rungsunn
Namjuntra, Pisit
author_sort Suriyaprom, Kanjana
collection PubMed
description BACKGROUND: Metabolic syndrome (MS) is a clinical constellation comprising risk factors associated with developing cardiovascular disease and type 2 diabetes. Resistin has been suggested as a linkage between obesity, inflammation and type 2 diabetes. This study aimed to investigate resistin concentrations and hematological-biochemical parameters in MS subjects and controls, and to determine whether two resistin gene (RETN) polymorphisms (−420C>G & +299G>A) are linked to resistin levels and MS among Thais. METHODS: This case-control study was performed with 322 Thai volunteers: 160 MS subjects and 162 controls. Anthropometric parameters and hematological-biochemical variables were determined. The RETN −420C>G (rs1862513) and +299G>A (rs3745367) polymorphisms were genotyped by PCR-RFLP technique. RESULTS: The resistin levels of the MS group were significantly higher than those of the control group. Resistin levels were positively correlated with anthropometric parameters and WBC count in the MS group. According to RETN −420C>G polymorphism, MS subjects with the G allele (CG/GG) (3.9 μg/L) had significantly higher resistin concentrations than in subjects with the CC genotype (2.4 μg/L); with regard to RETN +299G>A polymorphism, carriers with the A allele (GA/AA) (3.8 μg/L) had significantly higher resistin levels than subjects with the GG genotype (2.7 μg/L), after adjusting for potential covariates. However, the RETN −420C>G and +299G>A polymorphisms were not found to be associated with MS, hematological-biochemical parameters and anthropometric variables. CONCLUSIONS: These findings suggest resistin levels are linked with MS and the RETN −420C>G and +299G>A polymorphisms have impacted the circulating resistin concentrations. However, these two RETN polymorphisms probably do not influence susceptibility to MS among Thais.
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spelling pubmed-49223272017-03-29 Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais Suriyaprom, Kanjana Tungtrongchitr, Rungsunn Namjuntra, Pisit J Med Biochem Original Paper BACKGROUND: Metabolic syndrome (MS) is a clinical constellation comprising risk factors associated with developing cardiovascular disease and type 2 diabetes. Resistin has been suggested as a linkage between obesity, inflammation and type 2 diabetes. This study aimed to investigate resistin concentrations and hematological-biochemical parameters in MS subjects and controls, and to determine whether two resistin gene (RETN) polymorphisms (−420C>G & +299G>A) are linked to resistin levels and MS among Thais. METHODS: This case-control study was performed with 322 Thai volunteers: 160 MS subjects and 162 controls. Anthropometric parameters and hematological-biochemical variables were determined. The RETN −420C>G (rs1862513) and +299G>A (rs3745367) polymorphisms were genotyped by PCR-RFLP technique. RESULTS: The resistin levels of the MS group were significantly higher than those of the control group. Resistin levels were positively correlated with anthropometric parameters and WBC count in the MS group. According to RETN −420C>G polymorphism, MS subjects with the G allele (CG/GG) (3.9 μg/L) had significantly higher resistin concentrations than in subjects with the CC genotype (2.4 μg/L); with regard to RETN +299G>A polymorphism, carriers with the A allele (GA/AA) (3.8 μg/L) had significantly higher resistin levels than subjects with the GG genotype (2.7 μg/L), after adjusting for potential covariates. However, the RETN −420C>G and +299G>A polymorphisms were not found to be associated with MS, hematological-biochemical parameters and anthropometric variables. CONCLUSIONS: These findings suggest resistin levels are linked with MS and the RETN −420C>G and +299G>A polymorphisms have impacted the circulating resistin concentrations. However, these two RETN polymorphisms probably do not influence susceptibility to MS among Thais. Society of Medical Biochemists of Serbia 2015-04 2015-03-03 /pmc/articles/PMC4922327/ /pubmed/28356829 http://dx.doi.org/10.2478/jomb-2014-0034 Text en © by Kanjana Suriyaprom http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Original Paper
Suriyaprom, Kanjana
Tungtrongchitr, Rungsunn
Namjuntra, Pisit
Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title_full Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title_fullStr Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title_full_unstemmed Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title_short Associations of Resistin Levels with Resistin Gene Polymorphism and Metabolic Syndrome in Thais
title_sort associations of resistin levels with resistin gene polymorphism and metabolic syndrome in thais
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922327/
https://www.ncbi.nlm.nih.gov/pubmed/28356829
http://dx.doi.org/10.2478/jomb-2014-0034
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