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PMID: 10323402 Published · ppublish English Journal Article

Trp64Arg polymorphism of the beta3-adrenergic receptor gene in pregnancy: association with mild gestational diabetes mellitus.

The Journal of clinical endocrinology and metabolism ·Vol. 84 ·No. 5 ·1999-05-00 ·Pages 1695-9

Festa A, Krugluger W, Shnawa N, Hopmeier P, Haffner SM, Schernthaner G

Abstract

A missense mutation of the beta3-adrenergic receptor gene (Trp64Arg) has been associated with obesity and increased capacity to gain weight in nonpregnant populations. Furthermore, the mutation is a potential modifying factor in the etiology of impaired glucose tolerance and type 2 diabetes. We studied the relation of the beta3-adrenergic receptor genotype to glucose tolerance during pregnancy, a state of physiological insulin resistance. In 179 pregnant women (mean age, 28.5 +/- 0.4 yr), a 2-h oral glucose tolerance test was performed between gestational weeks 20 and 31. The beta3-adrenergic receptor genotype was assessed using restriction fragment length polymorphism. The frequency of the Arg64 allele was 9.15%. In women with mild gestational diabetes (n = 70), as defined by 60 min postload glucose values, the Trp64Arg genotype was more frequent than in women with normal glucose tolerance (n = 109; 26% vs. 11%; P = 0.01). Furthermore, the Trp64Arg polymorphism was associated with increased weight gain during pregnancy (baseline to gestational weeks 20-31) and increased postload glucose, insulin, and C peptide values during the oral glucose tolerance test. The results of the present study extend current knowledge about the association of the Trp64Arg beta3-adrenergic receptor polymorphism with glucose tolerance to a pregnant population. The association with mild gestational diabetes suggests that the impact of the polymorphism may be clinically important during pregnancy, a state of physiological insulin resistance.

MeSH Terms
Adult Arginine/genetics Body Weight Codon Diabetes, Gestational/genetics,physiopathology Female Glucose Tolerance Test Humans Lipids/blood Mutation, Missense Polymorphism, Genetic Pregnancy/genetics Receptors, Adrenergic, beta/genetics Receptors, Adrenergic, beta-3 Regression Analysis Reverse Transcriptase Polymerase Chain Reaction Tryptophan/genetics Weight Gain
Chemicals
Codon Lipids Receptors, Adrenergic, beta Receptors, Adrenergic, beta-3 Tryptophan Arginine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Festa A
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7873, USA. [email protected]
Krugluger W
Shnawa N
Hopmeier P
Haffner S M
Schernthaner G
Article Info
Journal
The Journal of clinical endocrinology and metabolism
Abbr.
J Clin Endocrinol Metab
ISSN
0021-972X
Published
1999-05-00
Pages
1695-9
Language
English
Region
United States
NLM ID
0375362
Subset
IM
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