ACE, PAI-1, decorin and Werner helicase genes are not associated with the development of renal disease in European patients with type 1 diabetes

Diabetes Metab Res Rev. 1999 Jul-Aug;15(4):247-53. doi: 10.1002/(sici)1520-7560(199907/08)15:4<247::aid-dmrr41>3.0.co;2-p.

Abstract

Background: Genetic factors are involved in the development of diabetic nephropathy in Type 1 diabetes. We have examined the association of four candidate genes, angiotensin converting enzyme (ACE): insertion/deletion (I/D) polymorphism, plasminogen activator inhibitor-1 (PAI-1): 4G/5G polymorphism, decorin: 179/183/185 polymorphism and Werner syndrome helicase: C/R polymorphism, with the presence of diabetic nephropathy in Type 1 diabetic patients.

Methods: 175 Type 1 diabetic patients with albuminuria (59 with microalbuminuria and 116 with macroalbuminuria) were compared with 136 Type 1 diabetic patients with normoalbuminuria and duration of disease longer than 15 years (mean+/-SD: 25+/-8 years). 200 non-diabetic subjects were also studied as background population.

Results: We found no association in the polymorphism of the four genes examined between patients with and without diabetic nephropathy and the control subjects.

Conclusions: The genes studied are unlikely to be involved in the susceptibility to nephropathy in Type 1 diabetic patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • DNA Helicases / genetics*
  • Decorin
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetic Nephropathies / genetics*
  • Exodeoxyribonucleases
  • Extracellular Matrix Proteins
  • Female
  • Genotype
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Peptidyl-Dipeptidase A / genetics*
  • Plasminogen Activator Inhibitor 1 / genetics*
  • Proteoglycans / genetics*
  • RecQ Helicases
  • United Kingdom
  • Werner Syndrome / enzymology
  • Werner Syndrome Helicase

Substances

  • DCN protein, human
  • Decorin
  • Extracellular Matrix Proteins
  • Plasminogen Activator Inhibitor 1
  • Proteoglycans
  • Exodeoxyribonucleases
  • Peptidyl-Dipeptidase A
  • DNA Helicases
  • RecQ Helicases
  • WRN protein, human
  • Werner Syndrome Helicase