Study of hereditary fructose intolerance by use of 31P magnetic resonance spectroscopy

Lancet. 1987 Oct 24;2(8565):931-4. doi: 10.1016/s0140-6736(87)91419-x.

Abstract

The effect of fructose on liver metabolism in patients with hereditary fructose intolerance (HFI) and in heterozygotes for HFI was studied by 31P magnetic resonance spectroscopy (31P-MRS). In patients with HFI (n = 5) ingestion of small amounts of fructose was followed by an increase in sugar phosphates and decrease in inorganic phosphate (Pi) in the liver that could be detected by 31P-MRS. 31P-MRS could be used to diagnose fructose intolerance and to monitor the patients' compliance with a fructose-restricted diet. In heterozygotes (n = 8) 50 g fructose given orally led to accumulation of sugar phosphates and depletion of Pi in the liver. Fructose also induced a larger increase in plasma urate in heterozygotes than in control subjects. The effect of fructose on liver Pi and plasma urate was most pronounced in heterozygotes with gout (n = 3). Heterozygosity for HFI may predispose to hyperuricaemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Metabolism, Inborn Errors / metabolism*
  • Female
  • Fructose / pharmacology
  • Fructose Intolerance / diagnosis
  • Fructose Intolerance / genetics
  • Fructose Intolerance / metabolism*
  • Fructose-Bisphosphate Aldolase / analysis
  • Fructosephosphates / analysis
  • Gout / metabolism
  • Heterozygote
  • Humans
  • Liver / metabolism
  • Magnetic Resonance Spectroscopy
  • Male
  • Phosphorus*
  • Uric Acid / blood

Substances

  • Fructosephosphates
  • fructose-1-phosphate
  • Uric Acid
  • Phosphorus
  • Fructose
  • Fructose-Bisphosphate Aldolase