[Treatment of type 1 hereditary haemochromatosis with oral magnesium]

Med Clin (Barc). 2006 Apr 29;126(16):611-3. doi: 10.1157/13087717.
[Article in Spanish]

Abstract

Background and objective: An essential step in the pathogenesis of hereditary hemochromatosis seems to be the increased expression of a duodenal divalent cation transporter (DMT1) responsible for absorption of non-heminic iron2+. The objective of the present study was to ascertain whether the competitive blockade of DMT1 by the administration of high doses of oral Mg2+ reduces iron absorption in patients homozygous for the C282Y mutation.

Patients and method: Iron absorption was evaluated by a low dose iron absorption test in 15 patients before and after treatment with oral magnesium (809.6 mg every 8 hours) for two weeks.

Results: We did not observe secondary effects or significant differences in iron absorption before or after magnesium treatment (14.7 micromol/L; 95% confidence interval [CI], 9.8-19.6 vs 14.9 micromol/L; 95% CI, 8.5-21.4, P = 0.7).

Conclusions: Treatment with oral magnesium does not reduce iron absorption in homozygous C282Y patients. This treatment can not be used in these subjects.

Publication types

  • Comparative Study
  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cation Transport Proteins / drug effects
  • Cation Transport Proteins / metabolism
  • Confidence Intervals
  • Female
  • Hemochromatosis / blood
  • Hemochromatosis / drug therapy*
  • Hemochromatosis / metabolism
  • Humans
  • Iron / blood
  • Iron / metabolism
  • Iron-Binding Proteins / drug effects
  • Iron-Binding Proteins / metabolism
  • Magnesium / therapeutic use*
  • Male
  • Middle Aged
  • Treatment Outcome

Substances

  • Cation Transport Proteins
  • Iron-Binding Proteins
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Iron
  • Magnesium