Aims: The allele frequencies of transcription factor 7 like 2 (TCF7L2) gene rs7903146 polymorphism in type 2 diabetes mellitus (T2DM) and non-T2DM controls were determined.

Methods: TCF7L2 rs7903146 genotypes were determined with qPCR.

Results: The TCF7L2 gene rs7903146 genotype frequencies for homozygous wild type (C/C), heterozygous (C/T) and homozygous polymorphic (T/T) for T2DM patients were determined, respectively, as 71.4%, 14.3%, 14.3% and 72.5%, 11.8%, 15.7% for controls. The weight, length and lean body mass were higher in C/T+T/T compared to C/C carriers. Glucose, insulin, insulin resistance and homeostatic model assessment (HOMA) were nonsignificantly higher in rs7903146C/T+T/T in comparison to C/C. TCF7L2 gene rs7903146 genotypes were not found to interact with drugs. The absence of any difference between genotype frequencies among study groups indicates that no association persists with TCF7L2 gene rs7903146 polymorphism and T2DM.

Conclusions: The effects of rs7903146 variation over some obesity variables suggest that this variation may effect T2DM development via obesity.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.dsx.2012.05.002DOI Listing

Publication Analysis

Top Keywords

gene rs7903146
20
tcf7l2 gene
16
transcription factor
8
rs7903146 variation
8
type diabetes
8
rs7903146 polymorphism
8
rs7903146 genotypes
8
genotype frequencies
8
rs7903146
7
gene
5

Similar Publications

Background: This study aims to investigate the genetic contribution of polymorphic variants of the () and () genes to the risk of developing prediabetes in individuals of Kazakh ethnicity.

Materials And Methods: This was a case-control study involving 200 cases with prediabetes and 200 prediabetes-free controls, aged 16-60 years ( = 400). Real-time polymerase chain reaction on a StepOnePlus instrument (Applied Biosystems, USA), employing the TaqMan method for site-specific amplification and genotyping of the () and () genes was used.

View Article and Find Full Text PDF

Background: A significant overlap in the pathophysiological features of polycystic ovary syndrome (PCOS) and type 2 diabetes mellitus (T2DM) has been reported; and insulin resistance is considered a central driver in both. The expression and hepatic clearance of insulin and subsequent glucose homeostasis are mediated by TCF7L2 via Wnt signaling. Studies have persistently associated TCF7L2 genetic variations with T2DM, however, its results on PCOS are sparse and inconsistent.

View Article and Find Full Text PDF

Background: India, with the largest population and second-highest type 2 diabetes mellitus (T2DM) prevalence, presents a unique genetic landscape. This study explores the genetic profiling of T2DM, aiming to bridge gaps in existing research and provide insights for further explorations.

Methods: We conducted a systematic review and meta-analysis of literature published up to September 2024 using databases like PubMed, Web of Science, Scopus, and Google Scholar to identify SNPs associated with T2DM in case-control studies within the Indian population.

View Article and Find Full Text PDF

The aim of this study was to conduct a comparative analysis of the population frequencies of the minor allele of polymorphic variants in the genes (rs7903146) and (rs1801282), based on the genome-wide association studies analysis data associated with the risk of developing prediabetes, in an ethnically homogeneous Kazakh population compared to previously studied populations worldwide. This study utilized a genomic database consisting of 1800 ethnically Kazakh individuals who were considered in healthy condition. Whole-genome genotyping was performed using Illumina OmniChip 2.

View Article and Find Full Text PDF
Article Synopsis
  • * The study focused on summarizing SNPs linked to these conditions specifically in Asian populations, as fewer studies have investigated this compared to Western populations.
  • * Key SNPs associated with obesity include rs9939609 and rs17782313 (FTO and MC4R genes), while T2DM is linked to SNPs like rs7903146 and rs12255372 (TCF7L2 gene), indicating the potential for gene screening in assessing risk for these diseases.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!