Leptin gene tetranucleotide repeat polymorphism in obese individuals in Egypt

Authors

  • Rizk Elbaz Genetics Unit, Mansoura Faculty of Medicine, Egypt
  • Nahed Dawood Faculty of Science, Tanta University, Egypt
  • Hala Mostafa Tanta University, Egypt
  • Somaia Zaki Tanta University, Egypt
  • Alaa Wafa
  • Ahmad Settin Mansoura University, Egypt

Abstract

Background: Leptin is a peptide hormone secreted by the adipose tissue. Genetic mutations of the leptin gene were reported to cause severe obesity.

Objectives: This study was undertaken to investigate the association of the polymorphic tetranucleotide repeat locus 3' UTR of leptin gene with obesity in Egyptian cases.

Subjects and Methods:  This study has included 120 subjects affected with obesity 57 of them were consistent with the diagnosis of metabolic syndrome (MS) while the rest (63) had simple obesity. These cases were compared to 83 normal weight healthy controls. All participants were subjected to an estimation of their body mass index (BMI), waist hip ratio (WHR), serum as well as characterization of leptin gene tetranucleotide repeat (TTTC)n polymorphism by PCR technique.

Results:  Thirteen different alleles were identified in all cases of obesity versus only 5 alleles in normal controls. The most frequent allele was the 154 bp allele (57.5% in all cases of obesity vs. 92.2% in controls). Total cases with obesity showed a significantly higher carriage rate of class II alleles (I/II + II/II genotypes) compared to healthy controls (48.3% vs. 6.0%, OR=14.6, 95% CI=5.5-38.6, p=<0.0001). This was more apparent in the group with simple obesity (52.3% vs. 6.0%, OR=17.2, 95% CI=6.1-48.1, p=<0.0001) than in MS cases (43.9 % vs. 6.0 %, OR =12.19, 95% CI=4.9-30.4, p=< 0.0001). Interestingly, cases with MS did not differ from those with simple obesity regarding their class I or II allele frequencies (p> 0.05). Although serum lipids were significantly higher in obese cases compared to controls, no difference was found among obese cases with different leptin gene class genotypes (p> 0.05).

Conclusions: Tetranucleotide repeat (TTTC)n polymorphism in the 3' UTR of the human leptin gene was associated with obesity in Egyptian obese cases showing higher class II allele carriage rate. However, the lipoprotein levels were not affected by this polymorphism.

Key words: Leptin gene; Obesity; Metabolic syndrome; Gene polymorphism.

 

Author Biographies

Rizk Elbaz, Genetics Unit, Mansoura Faculty of Medicine, Egypt

Associate Professor, Genetics Unit, Mansoura Faculty of Medicine, Egypt

Nahed Dawood, Faculty of Science, Tanta University, Egypt

Fellow, Zoology Department, Faculty of Science, Tanta University, Egypt

Hala Mostafa, Tanta University, Egypt

Professor, Zoology Department, Faculty of Science, Tanta University, Egypt

Somaia Zaki, Tanta University, Egypt

Professor, Zoology Department, Faculty of Science, Tanta University, Egypt

Ahmad Settin, Mansoura University, Egypt

Professor, Pediatrics and Genetics, Genetics Unit, Faculty of Medicine, Mansoura University, Egypt

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Published

2015-03-12

How to Cite

Elbaz, R., Dawood, N., Mostafa, H., Zaki, S., Wafa, A., & Settin, A. (2015). Leptin gene tetranucleotide repeat polymorphism in obese individuals in Egypt. International Journal of Health Sciences, 9(1). Retrieved from https://pub.qu.edu.sa/index.php/journal/article/view/964

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Original Paper