A pivotal role for beta-aminoisobutyric acid and oxidative stress in dihydropyrimidine dehydrogenase deficiency?

Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1103-6. doi: 10.1080/15257770600894097.

Abstract

Dihydropyrimidine dehydrogenase (DPD) constitutes the first step of the pyrimidine degradation pathway in which the pyrimidine bases uracil and thymine are catabolised to beta-alanine and beta-aminoisobutyric acid (beta-AIB), respectively. The mean concentration of beta-AIB was approximately 5- to 8-fold lower in urine of patients with a DPD deficiency, when compared to age-matched controls. Comparable levels of 8-hydroxydeoxyguanosine (8-OHdG) were present in urine from controls and DPD patients at the age <2 year. In contrast, slightly elevated levels of 8-OHdG were detected in urine from DPD patients with an age >2 year, suggesting the presence of increased oxidative stress.

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Aminoisobutyric Acids / metabolism*
  • Aminoisobutyric Acids / urine*
  • Case-Control Studies
  • Child, Preschool
  • Chromatography, High Pressure Liquid
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / chemistry
  • Dihydropyrimidine Dehydrogenase Deficiency*
  • Electrochemistry / methods
  • Humans
  • Infant
  • Oxidative Stress*
  • Purine-Pyrimidine Metabolism, Inborn Errors / diagnosis*
  • Purine-Pyrimidine Metabolism, Inborn Errors / genetics

Substances

  • Aminoisobutyric Acids
  • 8-Hydroxy-2'-Deoxyguanosine
  • Deoxyguanosine
  • 3-aminoisobutyric acid