Survey of Interleukin 10 Gene Promoter Polymorphisms at Position -592(A/C) and -1082 (A/G) in Obese Individuals with Type 2 Diabetes in north west of Iran

Publish Year: 1395
نوع سند: مقاله کنفرانسی
زبان: English
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IPMCMED01_072

تاریخ نمایه سازی: 23 آذر 1397

Abstract:

Backgrounds and Objectives: lots of genes are associated with the risk of developing diabetes. Overweight and obesity are common risk factors for type 2 diabetes (T2D) and most of the time body composition controlled by genetic factors. There are plenty of evidence to suggest that inflammatory reactions have a significant role in the incidence of these complications. Interleukin 10 is known as one of the most important anti-inflammatory cytokines. Thus, the present study was conducted to investigate the relationship between Interleukin 10 gene polymorphisms -592 A/C and -1082 A/G and susceptibility to get T2D and obesity.Materials and Methods: In this study, 75 obese patients with T2D, 75 non-obese patients with T2D, 75 obese patients without T2D and 75 healthy controls were studied. DNA extraction was carried out and then the genotype in -592 A/C and -1082A/G positions was determined using PCR-RFLP and chi squared test ( X2 ) was used as statistical methods for data analysis.Results: The frequency of CC and AC genotype in -592A/C position in obese patients with T2D and non-obese patients with T2D had more importance than non-diabetic patients (p<0.05). Also the frequency of AA genotype in -1082A/G position in obese patients with T2D was significantly more than other subjects (p<0.05) .Conclusion: Higher frequency of C allele in -592A/C position can be considered as a factor for T2D. Also the presence of an A allele next to C allele at the position of -592A/C could be predisposing of obesity in patients with T2D. Fewer frequency of haplotype AA/AA can be considered as a predisposing factor for obesity and T2D. Understanding the basis of this heterogeneity provides an opportunity for personalizing prevention and treatment strategies according to individual patient clinical and molecular characteristics.

Authors

Farzin Ferdousi

Department of Genetic,Biology Research Center,Zanjan Branch,Islamic Azad University,Zanjan,Iran

Amir Hossein Taromchi

Department of Biotechnology and Nanotechnology, Zanjan University of Medical Sciences, Zanjan, Iran

Abdolreza Esmaeilzadeh

Department of Immonology, Zanjan University of Medical Sciences, Zanjan, Iran