Association between a polymorphism in the angiotensin-converting enzyme gene and microvascular complications in Japanese patients with NIDDM

Diabetologia. 1996 Jan;39(1):97-102. doi: 10.1007/BF00400419.

Abstract

The relationship between diabetic nephropathy and an insertion (I)/deletion (D) polymorphism in intron 16 of the angiotensin-converting enzyme (ACE) gene is still under debate. The association of ACE gene polymorphism with nephropathy and retinopathy was therefore examined in 362 Japanese patients with non-insulin-dependent diabetes mellitus (NIDDM) and 105 healthy control subjects. Distribution of the ACE genotype did not differ between healthy control subjects and diabetic patients without complications. However, the frequency of the D allele was significantly higher in the diabetic subjects with nephropathy than in those without (0.32 in normoalbuminuric patients vs 0.44 in albuminuria patients with albuminuria) (chi 2 = 7.7; p = 0.006). There was no significant association between ACE genotype and retinopathy. These observations thus demonstrate a significant association of the ACE gene polymorphism with nephropathy, but not with retinopathy, in Japanese patients with NIDDM.

Publication types

  • Comparative Study

MeSH terms

  • Alleles
  • Base Sequence
  • DNA Primers
  • Diabetes Mellitus, Type 2 / enzymology
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Diabetic Angiopathies / enzymology
  • Diabetic Angiopathies / epidemiology
  • Diabetic Angiopathies / genetics*
  • Diabetic Nephropathies / genetics
  • Diabetic Nephropathies / therapy
  • Female
  • Genotype
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Peptidyl-Dipeptidase A / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Proteinuria
  • Reference Values
  • Renal Dialysis

Substances

  • DNA Primers
  • Peptidyl-Dipeptidase A