Association of angiotensin-converting enzyme gene insertion/deletion polymorphism with the clinico-pathological manifestations in immunoglobulin A nephropathy patients

Chin Med J (Engl). 1997 Jul;110(7):526-9.

Abstract

Objective: To investigate the relationship between angiotensin-converting enzyme (ACE) gene insertion/deletion polymorphism and the clinico-pathological manifestations in patients with immunoglobulin nephropathy (IgAN).

Methods: A flanking primer pair and an insertion-specific primer pair were used to perform two polymerase chain reactions so as to analyse the insertion/deletion polymorphism of ACE gene.

Results: There was a significantly higher genotype frequency for DD genotype in IgAN patients. The frequencies for DD genotype were also higher in those patients with hypertension and/or heavy proteinuria and/or severe glomerular sclerosis (P < 0.05).

Conclusions: We observed a significant association of the deletion polymorphism of ACE gene with renal insufficiency, hypertension and severe glomerular lesions at biopsy. The deletion allele may play a role, at least to some extent, in the deterioration and progression in IgA nephropathy.

MeSH terms

  • Adolescent
  • Adult
  • Alleles
  • Child
  • DNA Transposable Elements
  • Female
  • Gene Deletion
  • Glomerulonephritis, IGA / enzymology*
  • Glomerulonephritis, IGA / pathology
  • Humans
  • Kidney Failure, Chronic / enzymology
  • Male
  • Middle Aged
  • Peptidyl-Dipeptidase A / genetics*

Substances

  • DNA Transposable Elements
  • Peptidyl-Dipeptidase A