Renal parenchymal
scarring (RPS) following
urinary tract infection (UTI) is an important cause of renal morbidity in children. Studies have shown that the intensity of the inflammatory response following
infection is related to the risk of RPS. However, genetic variability in this response has not been studied. Adhesion molecules play a crucial role in leucocyte recruitment following
infection, and polymorphisms have been reported in the genes for key
cell adhesion molecules. We have investigated the possibility that children who develop RPS following UTI may exhibit altered genotype or allele frequencies for polymorphisms of the
intercellular adhesion molecule-1 (ICAM-1) (exons 4 and 6),
E-selectin (exons 2 and 4),
platelet endothelial cell adhesion molecule-1 (PECAM-1) (exon 3) and CD11b (
3'UTR) genes, which may predict outcome of UTI.
DNA was isolated from 99 children shown to have developed RPS, 43 children with no evidence of
scarring (NS) following UTI and 170 healthy controls. Genotyping was performed by restriction fragment length polymorphism (RFLP) analysis. When the RPS group was compared with the NS group, there was a significant reduction in the frequency of the
ICAM-1 exon 4 A allele (10.6 vs. 21.3%, respectively, chi2 = 6.01, P = 0.014). There was no significant difference in either allele or genotype frequency for any of the other polymorphisms studied. These data suggest that the A allele of the
ICAM-1 exon 4 polymorphism may protect against the risk of RPS following UTI and may participate in the regulation of the inflammatory response following UTI.