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The C825T polymorphism in the G-protein beta3 subunit gene and diabetic complications in IDDM patients.
- Source :
-
Journal of human genetics [J Hum Genet] 2001; Vol. 46 (4), pp. 188-91. - Publication Year :
- 2001
-
Abstract
- Complications of insulin-dependent diabetes mellitus (IDDM) are a major cause of morbidity and mortality; however, the mechanisms of their development are still to be elucidated. Genetic susceptibility contributes to the pathogenesis of nephropathy in IDDM. Enhanced G-protein activation, a cellular phenotype observed in cultured cells from patients with essential hypertension, was recently documented in IDDM subjects with nephropathy. A C825T polymorphism was recently described in GNB3, the gene encoding the beta 3 subunit of heterotrimeric G-proteins. This genetic variant has been associated with enhanced G-protein activation. The 825T allele was observed more frequently in a group with essential hypertension. We analyzed the role of the C825T polymorphism in the predisposition to diabetic complications in IDDM. In this study, we investigated the frequency of this polymorphism in a large case-control study and found no association of the 825T allele with diabetic nephropathy, retinopathy, and neuropathy.
- Subjects :
- Adolescent
Adult
Alleles
Case-Control Studies
Child
Child, Preschool
Cohort Studies
Diabetic Nephropathies etiology
Diabetic Nephropathies genetics
Diabetic Neuropathies etiology
Diabetic Neuropathies genetics
Diabetic Retinopathy etiology
Diabetic Retinopathy genetics
Female
Genetic Predisposition to Disease genetics
Genotype
Humans
Male
Middle Aged
Russia epidemiology
Diabetes Mellitus, Type 1 complications
Diabetes Mellitus, Type 1 genetics
Heterotrimeric GTP-Binding Proteins genetics
Polymorphism, Single Nucleotide genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1434-5161
- Volume :
- 46
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of human genetics
- Publication Type :
- Academic Journal
- Accession number :
- 11322658
- Full Text :
- https://doi.org/10.1007/s100380170087