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Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study
Aim: To identify genetic variants in promoter areas of IL-6 -174 G>C and TNF-α -308 G>A in metabolic syndrome (Met S) and controls and associate them with Met S and serum cytokine levels. It was a cross-sectional study, including 224 cases of Met S and 200 controls. A fasting blood sample was...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356053/ https://www.ncbi.nlm.nih.gov/pubmed/30635365 http://dx.doi.org/10.1042/BSR20181202 |
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author | Zafar, Uzma Khaliq, Saba Ahmad, Hafiz Usman Lone, Khalid Pervaiz |
author_facet | Zafar, Uzma Khaliq, Saba Ahmad, Hafiz Usman Lone, Khalid Pervaiz |
author_sort | Zafar, Uzma |
collection | PubMed |
description | Aim: To identify genetic variants in promoter areas of IL-6 -174 G>C and TNF-α -308 G>A in metabolic syndrome (Met S) and controls and associate them with Met S and serum cytokine levels. It was a cross-sectional study, including 224 cases of Met S and 200 controls. A fasting blood sample was taken and biochemical parameters including serum glucose, insulin, lipid profile, interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α) were measured. Restriction fragment length polymorphism was used to identify the genetic variants of IL-6 and TNF-α. Serum levels of IL-6 and TNF-α and insulin resistance were significantly higher in cases than the controls. IL-6 showed significant positive correlation with HOMA-IR and TNF-α. CC genotype of IL-6 was associated with the increased risk of Met S (P=0.016, OR for CC vs GC+GG = 2.33, CI: 1.15–4.71). There was no significant difference of TNF-α genotypes between the cases and the controls. Serum TNF-α and IL-6 levels were significantly higher in AA and CC genotypes of TNF-α (-308 G>A) and IL-6 (-174 G>C) as compared with the GG (P=0.00 and P=0.001). Significant correlation of IL-6 with TNF-α and insulin resistance was observed that may provide us a therapeutic target for preventing metabolic derangements from insulin resistance. |
format | Online Article Text |
id | pubmed-6356053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63560532019-02-05 Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study Zafar, Uzma Khaliq, Saba Ahmad, Hafiz Usman Lone, Khalid Pervaiz Biosci Rep Research Articles Aim: To identify genetic variants in promoter areas of IL-6 -174 G>C and TNF-α -308 G>A in metabolic syndrome (Met S) and controls and associate them with Met S and serum cytokine levels. It was a cross-sectional study, including 224 cases of Met S and 200 controls. A fasting blood sample was taken and biochemical parameters including serum glucose, insulin, lipid profile, interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α) were measured. Restriction fragment length polymorphism was used to identify the genetic variants of IL-6 and TNF-α. Serum levels of IL-6 and TNF-α and insulin resistance were significantly higher in cases than the controls. IL-6 showed significant positive correlation with HOMA-IR and TNF-α. CC genotype of IL-6 was associated with the increased risk of Met S (P=0.016, OR for CC vs GC+GG = 2.33, CI: 1.15–4.71). There was no significant difference of TNF-α genotypes between the cases and the controls. Serum TNF-α and IL-6 levels were significantly higher in AA and CC genotypes of TNF-α (-308 G>A) and IL-6 (-174 G>C) as compared with the GG (P=0.00 and P=0.001). Significant correlation of IL-6 with TNF-α and insulin resistance was observed that may provide us a therapeutic target for preventing metabolic derangements from insulin resistance. Portland Press Ltd. 2019-02-01 /pmc/articles/PMC6356053/ /pubmed/30635365 http://dx.doi.org/10.1042/BSR20181202 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Zafar, Uzma Khaliq, Saba Ahmad, Hafiz Usman Lone, Khalid Pervaiz Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title | Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title_full | Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title_fullStr | Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title_full_unstemmed | Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title_short | Serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
title_sort | serum profile of cytokines and their genetic variants in metabolic syndrome and healthy subjects: a comparative study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356053/ https://www.ncbi.nlm.nih.gov/pubmed/30635365 http://dx.doi.org/10.1042/BSR20181202 |
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