Back to Search Start Over

Association of IL- 6, TNF- α and IL- 10 gene polymorphisms with type 2 diabetes mellitus.

Authors :
Saxena, Madhukar
Srivastava, Neena
Banerjee, Monisha
Source :
Molecular Biology Reports; Nov2013, Vol. 40 Issue 11, p6271-6279, 9p
Publication Year :
2013

Abstract

Type 2 diabetes mellitus (T2DM) is a metabolic pro-inflammatory disorder characterized by chronic hyperglycemia and increased levels of circulating cytokines suggesting a causal role of inflammation in its etiology. Polymorphism of cytokine genes including interleukin-6 ( IL- 6), tumour necrosis factor- α ( TNF- α) and interleukin-10 ( IL- 10) were studied in T2DM patients as well as in normal healthy controls. Genomic DNA was isolated from both T2DM patients and controls followed by quantification and genotyping by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) using suitable primers. The genotypic, allelic and carriage rate frequency distribution in patients and controls were analyzed by SPSS (version 15.0). Odd ratios with 95 % confidence interval was determined to describe the strength of association by logistic regression model. Double and triple combinations of genotypes were analyzed by χ test. Gene-gene interaction and linkage disequilibrium tests were performed using SHEsis software. Individually, IL- 6, TNF- α and IL- 10 did not show any association. In double combination, IL- 6 −597 GA and TNF- α −308 GG genotypes increased the risk up to 21 times and in triple combination IL- 6 −597 AA, TNF- α −308 GG and IL- 10 −592 CA increased the risk of T2DM up to 314 times. In gene-gene interaction allele 'A' of all studied polymorphisms increased the risk of T2DM up to 1.41 times. Our results suggest that individuals having a haplotype combination of AA, GG and CA for IL- 6, TNF- α and IL- 10 gene polymorphisms will have higher susceptibility and be at greater risk of developing T2DM. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03014851
Volume :
40
Issue :
11
Database :
Complementary Index
Journal :
Molecular Biology Reports
Publication Type :
Academic Journal
Accession number :
91553355
Full Text :
https://doi.org/10.1007/s11033-013-2739-4