Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility
doi: 10.1620/tjem.200.155
pmid: 14521259
Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility
Kawasaki disease (KD) is a systemic vasculitis and occurs among Japanese children at a high incidence. Serum bilirubin and heme oxygenase-1 (HO-1) expression are known to play a significant role in the protection of vascular endothelial cells. Japanese have unique polymorphic distribution patterns of (TA)7 or G71R of the bilirubin UDP-glucuronosyltransferase (B-UGT) gene and of (GT)n repeats of the HO-1 gene. We investigated the relationship of KD susceptibility with these polymorphisms. There were no significant differences in the distribution of allele frequencies and genotypes of these polymorphisms between KD patients and controls. These polymorphisms are not associated with KD susceptibility.
- Yamagata University Japan
Adult, Heterozygote, Adolescent, Genotype, DNA Mutational Analysis, Homozygote, Infant, DNA, Gene Frequency, Japan, Child, Preschool, Heme Oxygenase (Decyclizing), Humans, Female, Genetic Predisposition to Disease, Glucuronosyltransferase, Child, Dinucleotide Repeats, Heme Oxygenase-1, Aged
Adult, Heterozygote, Adolescent, Genotype, DNA Mutational Analysis, Homozygote, Infant, DNA, Gene Frequency, Japan, Child, Preschool, Heme Oxygenase (Decyclizing), Humans, Female, Genetic Predisposition to Disease, Glucuronosyltransferase, Child, Dinucleotide Repeats, Heme Oxygenase-1, Aged
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