Relationship between DDAH gene variants and serum ADMA level in individuals with type 1 diabetes

  • Rhys D. Fogarty
  • , Sotoodeh Abhary
  • , Shahrbanou Javadiyan
  • , Nicholas Kasmeridis
  • , Nikolai Petrovsky
  • , Malcolm J. Whiting
  • , Jamie E. Craig
  • , Kathryn P. Burdon

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)195-198
Number of pages4
JournalJournal of Diabetes and Its Complications
Volume26
Issue number3
DOIs
Publication statusPublished or Issued - May 2012
Externally publishedYes

Keywords

  • ADMA
  • DDAH1
  • DDAH2
  • Diabetes

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

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