Investigation of 3111T/C polymorphism of the CLOCK gene in obese individuals with or without binge eating disorder: association with higher body mass index

Neurosci Lett. 2008 Apr 11;435(1):30-3. doi: 10.1016/j.neulet.2008.02.003. Epub 2008 Feb 9.

Abstract

Loss of circadian patterning of metabolism-related functions seems to play a role in the pathogenesis of obesity; therefore, it is reasonable to hypothesize that the functional 3111T/C single nucleotide polymorphism (SNP) of the (Circadian locomotor output cycles kaput) CLOCK gene may have a part in the genetic susceptibility to obesity. The aim of this study was to assess the frequencies of 3111T/C CLOCK gene SNP in overweight/obese subjects with or without binge eating disorder (BED) as compared to normal weight healthy controls. A total of 284 Caucasian subjects, including 92 normal weight healthy subjects and 192 overweight/obese patients (107 with BED) participated into the study. Genotype and allele frequencies did not significantly differ between normal weight controls and overweight/obese patients with and/or without BED. However, overweight/obese patients carrying the CC genotype had significantly higher values of body mass index (BMI) as compared to those carrying the CT and/or TT genotypes. Moreover, obese class III individuals had a significantly higher frequency of both the CC genotype and the C allele as compared to individuals with BMI<40 kg/m(2). Present findings show for the first time that the 3111T/C SNP of the CLOCK gene is not associated to human obesity and/or BED, but it seems to predispose obese individuals to a higher BMI.

MeSH terms

  • Adult
  • Body Mass Index*
  • Bulimia Nervosa / genetics*
  • Bulimia Nervosa / metabolism
  • Bulimia Nervosa / physiopathology
  • CLOCK Proteins
  • DNA Mutational Analysis
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genotype
  • Humans
  • Male
  • Obesity / genetics*
  • Obesity / metabolism
  • Obesity / physiopathology
  • Polymorphism, Genetic / genetics*
  • Trans-Activators / genetics*

Substances

  • Trans-Activators
  • CLOCK Proteins
  • CLOCK protein, human