5-HT2A receptor gene polymorphism is associated with food and alcohol intake in obese people

Int J Obes Relat Metab Disord. 2000 Jul;24(7):920-4. doi: 10.1038/sj.ijo.0801253.

Abstract

Objective: To test the association between a polymorphism of the 5-HT2A receptor gene, -1438G/A, and energy and nutrients intake, including alcohol.

Subjects: Two hundred and seventy six unrelated overweight subjects (180 women, 96 men) were recruited from the Nutrition Department of Bichat Hospital in Paris on the basis of 120% of ideal body weight (body mass index, BMI=33.3+/-4.8 kg/m2). A second overweight sample (31 women, 49 men) was drawn from the Stanislas Family Study, composed of volunteers for a free health examination in Nancy (BMI=29.6+/-3.1 kg/m2).

Measurements: Energy and nutrients intake were assessed using the diet history method in Paris and the 3-day record method in Nancy. We analyzed the polymorphism by PCR followed by MspI digestion. Statistical differences between genotypes were assessed by using the non-parametric Kruskal-Wallis test.

Results: In the whole overweight population, the A allele was associated with lower energy intake 10. 3+/-2.8, 9.9+/-2.8, 9.3+/-2.9 MJ/day for GG, GA and AA genotypes respectively (P<0.05). This association was significant in the patient sample from Paris and in the overweight male volunteers from Nancy. Allele A-related lowering in energy intake was due to a trend to lower intakes in all the main nutrients. The A allele was also associated with a lower alcohol consumption: 18.4+/-19.7, 15.3+/-21. 2 and 12.3+/-17.5 g/day for GG, GA and AA genotypes, respectively (P<0.05).

Conclusions: These data indicate that a gene polymorphism may influence food and alcohol intake in overweight humans. This could be explained by the role of the serotonergic system as a determinant of food intake.

MeSH terms

  • Adult
  • Alcohol Drinking / genetics*
  • Body Mass Index
  • Diet Records
  • Eating / genetics*
  • Eating / physiology
  • Energy Intake / genetics
  • Female
  • Humans
  • Male
  • Middle Aged
  • Obesity / genetics*
  • Obesity / physiopathology
  • Polymorphism, Genetic
  • Receptors, Serotonin / genetics*
  • Receptors, Serotonin / physiology

Substances

  • Receptors, Serotonin