Abstract
Phlebotomy constitutes the established treatment for HFE-related hemochromatosis. Retrospective studies have suggested proton pump inhibitors (PPIs) reduce the need for phlebotomy in this population. We conducted a randomized controlled trial to prove this. Thirty p.C282Y homozygous patients were randomly allocated to PPI (pantoprazole 40 mg/day) or placebo for 12 months. Phlebotomies were performedwhen serum ferritin was >100 mu g/L. Phlebotomy need turned out to be significantly lower in patients taking PPI (P = .0052). PPI treatment significantly reduces the need for phlebotomies in p.C282Y homozygous patients. In view of the known long-term safety profile of PPI, they can be a valuable addition to standard therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 678-680.e2 |
| Number of pages | 5 |
| Journal | Gastroenterology |
| Volume | 153 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Sept 2017 |
Keywords
- Hereditary Hemochromatosis
- Proton Pump Inhibitors
- Randomized Clinical Trial
- HEREDITARY HEMOCHROMATOSIS
- IRON
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