Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria

Am J Nephrol. Mar-Apr 2005;25(2):183-8. doi: 10.1159/000085411. Epub 2005 Apr 21.

Abstract

Background: Marked hyperoxaluria due to liver-specific deficiency of alanine:glyoxylate aminotransferase activity (AGT) characterizes type I primary hyperoxaluria (PHI). Approximately half of PHI patients experience improvement in the degree of hyperoxaluria following pyridoxine (VB6) treatment. Recently, we showed an association between VB6 response and the commonest PHI mutation G170R, with patients possessing one or two copies showing 50% reduction or complete to near complete normalization of oxaluria, respectively. Two patients showed responses varying from this pattern. To further clarify the molecular basis of VB6 response in PHI, we performed additional genotyping.

Methods: 23 PHI patients diagnosed via hepatic enzyme analysis, hyperoxaluria and hyperglycolic aciduria or homozygosity for a known mutation, availability of pre- and post-VB6 24-hour urine oxalate and GFR >40 ml/min/1.73 m2 were included. Data was retrieved retrospectively, oxalate measured by oxalate oxidase, and genotyping performed by PCR-based methods.

Results: VB6 response was associated with the G170R and F152I mutations. Eight new sequence changes were detected.

Conclusions: In PHI, two mutations resulting in AGT mistargeting are associated with VB6 response. Whether this favorable effect is specific to the peroxisomal-to-mitochondrial mistargeting caused by these changes or due to another mechanism remains to be determined.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cohort Studies
  • Enzymes / genetics*
  • Genotype
  • Humans
  • Hyperoxaluria, Primary / drug therapy
  • Hyperoxaluria, Primary / genetics*
  • Phenotype
  • Pyridoxine / therapeutic use*
  • Retrospective Studies
  • Vitamins / therapeutic use*

Substances

  • Enzymes
  • Vitamins
  • Pyridoxine