Nephrol Dial Transplant (2002) 17: 652-654
© 2002 European Renal Association-European Dialysis and Transplant Association
Brief Report
The deletion polymorphism of the ACE gene is not an independent risk factor for renal scarring in children with vesico-ureteric reflux
1 Departments of Paediatric Nephrology and 2 Cytogenetics, Southmead Hospital, Bristol, UK
Background. The deletion (D) polymorphism of the gene encoding angiotensin-I converting enzyme has been implicated as a risk factor for progressive renal disease in several conditions. This study was designed to evaluate the association between homozygosity for the D allele and susceptibility to renal scarring in children with vesico-ureteric reflux (VUR).
Methods. Two-hundred-and-six children with VUR (all grades) were recruited into the study. Patients were stratified into two groups according to the presence or absence of renal scarring. One-hundred-and-twelve patients (group 1) had evidence of renal scarring. Ninety-four children had no evidence of renal scarring (group 2). ACE genotypes were determined by polymerase chain reaction (PCR) amplification of genomic DNA samples.
Results. There was no association between the DD polymorphism and the presence of renal scarring. Genotype frequencies in group 1 were: II, 29; ID, 56; and DD, 27; and in group 2 were: II, 12; ID, 52; DD, 30 (P=0.21). Neither was there evidence supporting a dominant D allele. There was no association between the DD genotype and the presence of proteinuria or reduced renal function (P>0.05). Hypertension was seen more frequently in those individuals with the DD genotype, compared with the other two genotypes (P=0.012).
Conclusion. We cannot confirm previous reports that children with vesico-ureteric reflux who are homozygous for the deletion polymorphism of the ACE gene are more susceptible to renal scarring than heterozygotes and II homozygotes.
Keywords: ACE gene polymorphisms; renal scarring; vesico-ureteric reflux
Correspondence and offprint requests to: Dr J Dudley, Academic Department of Transplantation Sciences, Paul OGorman Lifeline Building, Southmead Hospital, Bristol BS10 5NB, UK. Email: jandudley{at}yahoo.com