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Relationship between DDAH gene variants and serum ADMA level in individuals with type 1 diabetes
- Source :
- Journal of diabetes and its complications. 26(3)
- Publication Year :
- 2011
-
Abstract
- Asymmetric dimethylarginine (ADMA) levels are elevated in diabetes and likely contribute to diabetic complications such as retinopathy and nephropathy. The DDAH enzymes are primarily responsible for ADMA metabolism. Polymorphisms in the dimethylarginine dimethylaminohydrolase (DDAH) 1 and 2 genes have been previously associated with serum ADMA levels in type 2 diabetes (T2DM). We sought to determine whether they are also associated with ADMA levels in individuals with type 1 diabetes (T1DM). Serum ADMA concentrations were measured in 196 individuals with T1DM. Twenty-six tag SNPs in the DDAH1 gene and 10 in the DDAH2 gene were genotyped. One SNP in the DDAH1 gene (rs3738111) and one in the DDAH2 gene (rs805293) showed a correlation with serum ADMA levels; however, neither survived correction for multiple testing. We found limited evidence that genetic polymorphisms in DDAH genes influence serum ADMA levels in individuals with T1DM. This differs to findings in T2DM and may be due to underlying differences in the cohorts or to fundamental differences in the pathogenesis of the two types of diabetes.
- Subjects :
- Adult
Male
medicine.medical_specialty
Genotype
Endocrinology, Diabetes and Metabolism
Single-nucleotide polymorphism
Type 2 diabetes
Arginine
Polymorphism, Single Nucleotide
Nephropathy
Amidohydrolases
Pathogenesis
Cohort Studies
Diabetes Complications
chemistry.chemical_compound
Endocrinology
Internal medicine
Diabetes mellitus
Internal Medicine
medicine
SNP
Humans
Genetic Predisposition to Disease
Genetic Association Studies
Aged
Type 1 diabetes
business.industry
Middle Aged
medicine.disease
Diabetes Mellitus, Type 1
chemistry
Female
business
Asymmetric dimethylarginine
Subjects
Details
- ISSN :
- 1873460X
- Volume :
- 26
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Journal of diabetes and its complications
- Accession number :
- edsair.doi.dedup.....f916506ffb71d9d8bc9c4ca02352856d