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Association between Trp48Arg polymorphism of the CD11c gene and risk for obesity among Iranian population

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Abstract

Background

Despite assessing the expression of CD11c gene in macrophages in adipose tissues and suggesting association between the gene expressions and predisposing to obesity, the relationship of the changes in CD11c gene and its variants with obesity has not been exclusively evaluated. The present study aimed to assess the relationship between rs2230424 gene polymorphism leading a single amino acid Arginine 48 to Tryptophan interchange in CD11c gene protein chain and obesity in a sample of Iranian population.

Methods

This case-control association study was performed on 247 subjects including obese individuals and a sex- and age-matched healthy non-obese individuals. After DNA extraction, the DNA sequence containing the relevant polymorphic site was amplified by polymerase chain reaction (PCR). Determining different genotypic patterns of the SNP was carried out by restriction fragment length polymorphism (RFLP) analysis. To final draft the suspected genotypes of the SNP, DNA sequencing was performed.

Results

The frequency of wild genotype (TT) of Trp48Arg polymorphism of the CD11c gene in obese and non-obese groups was 97.9% and 94.6% and the frequency of heterozygous genotype (TC) was 2.1% and 5.4%, respectively with no significant difference (p = 0.230,). None of the participants had mutant genotypic pattern of the polymorphism. There was no association of the genotypic pattern of Trp48Arg polymorphism with different underlying risk factors as well as mean laboratory parameters.

Conclusion

The presence of Trp48Arg polymorphism of the CD11c gene is not associated with increased risk for obesity among Iranian population.

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Correspondence to Shirin Hasani-Ranjbar.

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Talaschian, M., Amoli, M.M., Enayati, S. et al. Association between Trp48Arg polymorphism of the CD11c gene and risk for obesity among Iranian population. J Diabetes Metab Disord 17, 197–201 (2018). https://doi.org/10.1007/s40200-018-0361-7

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  • DOI: https://doi.org/10.1007/s40200-018-0361-7

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