Impact of Bloodletting on Iron Metabolism in Type 1 Hemochromatosis
- Conditions
- Hemochromatosis Type 1
- Registration Number
- NCT01810965
- Lead Sponsor
- Rennes University Hospital
- Brief Summary
Hemochromatosis type 1 is one of the most frequent genetic disease since the genetic predisposition (homozygosity for the C282Y mutation of the HFE gene) is encountered in about 3/1000 white subjects (5/1000 in Brittany, France).
For the half of these predisposed subjects, the phenotypic expression of the disease needs a treatment. This treatment is based upon repeated bloodletting which is generally considered as simple, safe and effective.
Nevertheless, it is still questioned as regard its physiopathological justification and its clinical implications. Indeed, bloodletting could cause an increase of non-transferrin bound iron (NTBI) particularly for its reactive form called labile plasma iron (LPI) This adverse physiopathological effect could have clinical consequences and could be linked with articular consequences which can be aggravated by the treatment.
- Detailed Description
Hemochromatosis type 1 is one of the most frequent genetic disease since the genetic predisposition (homozygosity for the C282Y mutation of the HFE gene) is encountered in about 3/1000 white subjects (5/1000 in Brittany, France).
For the half of these predisposed subjects, the phenotypic expression of the disease needs a treatment. This treatment is based upon repeated bloodletting which is generally considered as simple, safe and effective.
Nevertheless, it is still questioned as regard its physiopathological justification and its clinical implications. Indeed, bloodletting could cause an increase of non-transferrin bound iron (NTBI) particularly for its reactive form called labile plasma iron (LPI) This adverse physiopathological effect could have clinical consequences and could be linked with articular consequences which can be aggravated by the treatment.
The primary objective is to explore the effect of bloodletting upon plasmatic concentrations of NTBI.
The secondary objectives are to:
* explore the impact of bloodletting upon different parameters of iron metabolism and in particular LPI, hepcidinemia and markers of erythropoiesis ;
* explore basal and nycthemeral characteristics of new parameters of iron metabolism (hepcidin, NTBI, LPI) in hemochromatosis patients.
The demonstration of an adverse effect of bloodletting upon iron metabolism would allow for a therapeutic innovation based upon an association of bloodletting and oral chelation during the induction treatment of type 1 hemochromatosis and, more generally in hepcidino deficient forms of hemochromatosis.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 6
- Men
- Age 18 years or older
- Homozygosity for the C282Y mutation of the HFE gene
- With an indication of treatment by bloodletting (in accordance with the French HAS guidelines)
- Ferritinemia ≥ 500µg/L
- Transferrin saturation ≥ 75%
- Never treated by bloodletting
- Written informed consent
- Contraindication to bloodletting
- Chronic inflammatory or dysmetabolic or neoplastic disease
- Major cardiovascular disease
- Excessive consumption of alcohol (≥ 3gr/day)
- Treatment by iron chelators, C or E vitamins
- Stay in altitude> 1500m in the month preceding the period Day 1
- Patients under guardianship
- Blood donation in the 3 past months
- Night / shift workers
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Maximal variation (delta maximum) of NTBI during the 5 days following a bloodletting Day 5
- Secondary Outcome Measures
Name Time Method Kinetic of LPI plasmatic concentration during the 5 days following a bloodletting Day 5 Kinetic of hepcidin plasmatic concentration during the 5 days following a bloodletting Day 5 Hemoglobin Day 9, day 10, day 11 and day 12 Circadian kinetic of hepcidine plasmatic concentration when no bloodletting is performed Day 1 Maximal variation (delta maximum) of LPI during the 5 days following a bloodletting Day 5 CRP Day 9, day 10, day 11 and day 12 EPO Day 9, day 10, day 11 and day 12 Kinetic of transferrin saturation during the 5 days following a bloodletting Day 5 Maximal variation (delta maximum) of hepcidin during the 5 days following a bloodletting Day 5 Soluble transferrin receptor Day 9, day 10, day 11 and day 12 Circadian kinetic of NTBI plasmatic concentration when no bloodletting is performed Day 1 Circadian kinetic of API plasmatic concentration when no bloodletting is performed Day 1 Maximal variation (delta maximum) of transferrin saturation during the 5 days following a bloodletting Day 5 Kinetic of NTBI plasmatic concentration during the 5 days following a bloodletting Day 5
Trial Locations
- Locations (1)
CHU Pontchaillou
🇫🇷Rennes, France