Leptin receptor Gln223Arg variant is associated with a cluster of metabolic abnormalities in response to long-term overfeeding

J Intern Med. 2000 Nov;248(5):435-9. doi: 10.1046/j.1365-2796.2000.00751.x.

Abstract

Objectives: The role of the leptin receptor (LEPR) gene Gln223Arg polymorphism on the metabolic and body composition changes in response to overfeeding was studied.

Subjects: Twelve pairs of male monozygotic twins ate a 4.2 MJ day-1 energy surplus, 6 days week-1, during a period of 100 days.

Results: Overfeeding induced a significantly greater increase in glucose (P = 0.001 for percentage change) and insulin (P = 0.038) areas under the curve during oral glucose tolerance tests (OGTTs) in the GlnGln (n = 10) than in the GlnArg/ArgArg (n = 14) subjects. In addition, the GlnGln genotype was associated with a greater increase in plasma levels of leptin (P = 0.037) and total triglycerides (P = 0.003), as well as a greater decrease in high-density lipoprotein cholesterol (P = 0.010), than for the combined GlnArg/ArgArg genotypes. Body composition changes were not different between the genotypes.

Conclusions: We conclude that the GlnGln subjects of the LEPR gene polymorphism are more susceptible to metabolic abnormalities when they are exposed to long-term positive energy balance. These findings provide new information on the genetic basis of individual differences in response to chronically elevated food intake.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Twin Study

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Body Weight
  • Cholesterol / blood
  • Genotype
  • Humans
  • Hyperphagia / genetics
  • Hyperphagia / metabolism*
  • Insulin / blood
  • Male
  • Phenotype
  • Polymorphism, Genetic
  • Receptors, Cell Surface / genetics*
  • Receptors, Leptin
  • Twins, Monozygotic

Substances

  • Blood Glucose
  • Insulin
  • LEPR protein, human
  • Receptors, Cell Surface
  • Receptors, Leptin
  • Cholesterol