β3-Adrenergic receptor gene polymorphism and type 2 diabetes in a Caucasian population

A.M. Oeveren van-Dybicz, Harald Erwin Vonkeman, M.A.M. Bon, F.A.J.T.M. van den Bergh, I. Vermes

    Research output: Contribution to journalArticleAcademic

    17 Citations (Scopus)
    8 Downloads (Pure)

    Abstract

    Aim: The β3-adrenergic receptor (β3-AR) is suspected to play a key role in the regulation of energy balance by increasing lipolysis and thermogenesis. A mutation in the β3-AR gene (Trp64Arg) has been associated with the capacity of weight gain and with early onset of noninsulin dependent diabetes mellitus (type 2 diabetes). In this study we investigated the prevalence of the two β3-AR alleles in a Caucasian population and studied the association between the β3-AR genotype and metabolic disorders (obesity and type 2 diabetes). - Methods: Genomic DNA extracted from peripheral blood leucocytes of 200 Caucasian subjects (137 subjects with and 63 subjects without type 2 diabetes). The MvaI polymorphism of β3-AR, which detects the Trp64Arg mutation, was determined by polymerase chain reaction (PCR). We studied the correlation between the Trp64Arg mutation and the body mass index (b.m.i. kg/m2). - Results: There was no significant difference between the patients with type 2 diabetes and control subjects in the frequency of the Arg64 allele (5.5% and 4.8%, respectively). Within the group of type 2 diabetes patients were 14 subjects with the Trp64Arg mutation (b.m.i., mean ± s.d.: 31 ± 8.5 kg/m2) and 123 without the mutation (b.m.i. 29 ± 4.8). There was no association between the β3-AR gene polymorphism and sex, obesity, blood pressure, glycohaemoglobin concentration, proteinuria. - Conclusion: Our results suggest that the Trp64Arg mutation is not a major determinant of metabolic disorders (type 2 diabetes, obesity) and chronic complications of type 2 diabetes in a Dutch population
    Original languageUndefined
    Pages (from-to)47-51
    JournalDiabetes, Obesity and Metabolism
    Volume3
    Issue number1
    DOIs
    Publication statusPublished - 2008

    Keywords

    • IR-72549

    Cite this