Summary:
Beta-3-adrenergic receptor (beta-3-AR) and insulin receptor substrate 1 (IRS-1) have
been implicated in the pathogenesis of obesity and in obesity related increase in
insulin resistance which is associated with, among other diseases, dyslipidemia and
type 2 diabetes mellitus. We studied 210 white female Caucasian obese subjects, who
underwent a formal weight loss program (Optifast®). We examined the association between
mutations of the IRS-1 gene at codon 972, mutations of the beta-3-AR gene at codon
64, and the combination of both mutations with the degree of weight loss, waist to
hip ratio and the prevalence of hypertension, dyslipidemia and type 2 diabetes mellitus.
Twenty-four women (11.4%) were polymorph only for the beta-3-AR mutation, 23 women
(10.9%) only for the IRS-1 mutation, and 6 subjects (2.9%) were polymorph for both
alleles. No patient displayed a homozygous polymorphism. Similar frequencies of these
polymorphisms were observed when the 100 non-obese control women were tested (14.0,
15.0, 3.0, respectively). After 13 weeks of weight loss the group with multiple polymorph
alleles had lost less of their weight than the obese controls without mutation (Delta
BMI 5.32 ± 0.18 versus 6.12 ± 0.2 kg/m2 , p < 0.05). In this group, the frequency of type 2 diabetes (66.7%) was significantly
higher than in the obese control group without mutations (16.7%, p = 0.008).
Our findings suggest there is a synergy between the polymorphisms of Trp64Arg beta-3-AR
and Gly972Arg IRS-1 in Caucasian German obese women leading to a decreased weight
loss. This seems to be accompanied with an increased frequency of type 2 diabetes.
Abbreviations: beta-3-AR = beta-3-adrenergic receptor, IRS-1 = insulin receptor substrate 1, BMI
= body mass index
Key words:
Obesity - beta-3-adrenergic - IRS-1
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1 Statistical analysis was performed using Student's t-test (*) or using Chi-square
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2 * p = 0.01, Chi-square test
3 * p < 0.05 using MANOVA compared with baseline
4 ‡ p < 0.05 using ANOVA compared with obese controls at the same time
Dr. med. Heike Benecke
Abt. Klinische Endokrinologie
Zentrum Innere Medizin und Dermatologie
Medizinische Hochschule Hannover
Carl-Neuberg-Strasse 1
D-30623 Hannover
Phone: +49-511-532-3822
Fax: +49-511-532-3825