S. Schmidt et al., NO ASSOCIATION OF CONVERTING-ENZYME INSERTION DELETION POLYMORPHISM WITH IMMUNOGLOBULIN-A GLOMERULONEPHRITIS, American journal of kidney diseases, 26(5), 1995, pp. 727-731
has been recently reported that in type 1 diabetes the insertion/delet
ion (I/D) polymorphism of the angiotensin l-converting enzyme gene is
associated with the presence of diabetic nephropathy, Tissue angiotens
in I-converting enzyme is determined by I/D polymorphism, and it has b
een speculated that in diabetes differences of local angiotensin II av
ailability determine the risk of renal disease, Since angiotensin II i
s thought to play an important role in the evolution of renal disease
in general, we tested whether genotype distribution of the I/D polymor
phism is also different in patients with immunoglobulin A-glomerulonep
hritis (IgA-GN). Furthermore we compared IgA-GN patients with (1) stab
le renal function or (2) terminal renal failure to investigate a poten
tial role of the I/D polymorphism in the renal prognosis, We examined
122 patients with biopsy-confirmed IgA-GN who had stable renal functio
n and 82 dialysis-dependent or transplanted patients with biopsy-confi
rmed IgA-GN, Furthermore, in 134 healthy individuals used as controls
we analyzed the DNA for normal distribution of genotypes and allele fr
equencies, The polymorphic region was amplified using polymerase chain
reaction with specific primers. Alleles were detected on 2% agarose g
els, Genotype distributions and allele frequencies were not significan
tly different between controls and patients with IgA-GN and stable ren
al function, Furthermore, no significant difference in genotype distri
bution was detected between patients with IgA-GN and stable renal func
tion compared with patients with IgA-GN and end-stage renal failure, a
lthough a trend for a higher frequency of DD-homozygotes was noted in
the latter group (P = 0.07), We conclude that the genotype distributio
n of the I/D polymorphism is not changed in IgA-GN. To firmly establis
h whether it is related to the risk of progression, further studies wi
th larger patient samples are required. (C) 1995 by the National Kidne
y Foundation, Inc.