Beta 3-adrenoreceptor gene polymorphism and leptin. Lack of relationship in type 2 diabetic patients

Clin Endocrinol (Oxf). 1998 Nov;49(5):679-83. doi: 10.1046/j.1365-2265.1998.00599.x.

Abstract

Introduction: The beta 3-Adrenergic receptor (beta 3AR) and leptin are molecules involved in the regulation of energy balance. Recently, a mutation in the beta 3AR gene (Trp64Arg) has been reported to be associated with features of insulin resistance, weight gain and early onset of Type 2 Diabetes Mellitus. The aim of this study was to determine the frequency and clinical characteristics of the Trp64Arg mutation in the beta 3AR gene in Type 2 diabetic patients, its relationship with leptin levels, and its role in microangiopathic complications.

Subjects and methods: 187 Type 2 diabetic patients and 100 unrelated non-diabetic subjects were studied. There was no difference between the diabetic and nondiabetic subjects in the frequency of the Trp64 and Arg64 alleles (92.5% vs. 92.3% and 7.5% vs. 7.7%, respectively). Type 2 diabetic patients were divided into two groups according to the presence (n = 27) or absence of the mutation (n = 160).

Results: Mutation of the beta 3AR gene was not associated with any differences either in the clinical and metabolic parameters or microangiopathic complications. Type 2 diabetic patients carrying the Arg64 allele tended to have a lower diabetes duration, but this was not statistically significant. Plasma leptin levels were not different according to the beta 3AR genotype.

Conclusions: The Trp64Arg mutation is not a major determinant of Type 2 diabetes and its microangiopathic complications. Moreover, this mutation was not clinically relevant in leptin regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles
  • Blood Pressure / genetics
  • Body Mass Index
  • Case-Control Studies
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism*
  • Diabetic Nephropathies / genetics
  • Diabetic Nephropathies / metabolism
  • Diabetic Retinopathy / genetics
  • Diabetic Retinopathy / metabolism
  • Female
  • Humans
  • Leptin
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Proteins / metabolism*
  • Receptors, Adrenergic, beta / genetics*
  • Receptors, Adrenergic, beta-3
  • Receptors, Leptin
  • Statistics, Nonparametric

Substances

  • LEPR protein, human
  • Leptin
  • Proteins
  • Receptors, Adrenergic, beta
  • Receptors, Adrenergic, beta-3
  • Receptors, Leptin