No association of LEPR Gln223Arg polymorphism with leptin, obesity or metabolic disturbances in children

Eur J Med Res. 2009 Dec 7;14 Suppl 4(Suppl 4):201-4. doi: 10.1186/2047-783x-14-s4-201.

Abstract

Objective: The aim of the study was to investigate whether the Gln223Arg in the leptin receptor may influence body weight, leptin concentration, and metabolic parameters in children.

Materials and methods: The examined group included 101 obese children (58 girls and 43 boys) with BMI 31.41 +/-5.03 kg/m(2) (BMI > or = 2 SDS) and the control group consisted of 41 children with BMI 20.0 +/-0.80 kg/m2 (BMI <1.0 SDS). Polymorphism identification was performed in total genomic DNA using PCR-RFLP method.

Results: The distribution of genotypes LEPR was the following: in the obese group: AA - 20.8%, AG- 55.4%, GG-23.8 %; in the control group AA-31.7%, AG- 53.65%, GG-14.65%. Comparative analyses between AA homozygous children and carriers of G alleles did not confirm any relation between the analyzed polymorphism and BMI, leptin concentrations, and metabolic disturbances in children with obesity.

Conclusion: In children with obesity we did not observe association of the LEPR Gln223Arg gene polymorphism with obesity, leptin, insulin resistance, and metabolic abnormalities.

MeSH terms

  • Adolescent
  • Body Mass Index
  • Child
  • Female
  • Humans
  • Insulin / blood
  • Insulin Resistance
  • Leptin / blood*
  • Male
  • Metabolic Diseases / genetics*
  • Obesity / blood
  • Obesity / genetics*
  • Polymorphism, Genetic*
  • Receptors, Leptin / genetics*

Substances

  • Insulin
  • Leptin
  • Receptors, Leptin