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Blood donation for iron removal in individuals with HFE mutations: study of efficacy and safety and short review on hemochromatosis and blood donation.
Infanti, Laura; Leitner, Gerda; Moe, Morten; Pehlic, Vildana; Cattaneo, Marco; Benkert, Pascal; Holbro, Andreas; Passweg, Jakob; Worel, Nina; Buser, Andreas.
Afiliación
  • Infanti L; Regional Blood Transfusion Centre Swiss Red Cross Basel, Basel, Switzerland.
  • Leitner G; Division of Hematology, University Hospital, University of Basel, Basel, Switzerland.
  • Moe M; Austrian Red Cross, Vienna, Austria.
  • Pehlic V; Unit of Medical Biochemistry, Division of Diagnostics and Technology, Akershus University Hospital, Akershus, Norway.
  • Cattaneo M; Regional Blood Transfusion Centre Swiss Red Cross Basel, Basel, Switzerland.
  • Benkert P; Clinical Trial Unit, Department of Clinical Research, University and University Hospital Basel, Basel, Switzerland.
  • Holbro A; Clinical Trial Unit, Department of Clinical Research, University and University Hospital Basel, Basel, Switzerland.
  • Passweg J; Regional Blood Transfusion Centre Swiss Red Cross Basel, Basel, Switzerland.
  • Worel N; Division of Hematology, University Hospital, University of Basel, Basel, Switzerland.
  • Buser A; Division of Hematology, University Hospital, University of Basel, Basel, Switzerland.
Front Med (Lausanne) ; 11: 1362941, 2024.
Article en En | MEDLINE | ID: mdl-38566922
ABSTRACT

Background:

Elevated serum ferritin with/without HFE variants in asymptomatic persons leads frequently to referral for blood donation. Hemochromatosis (p.C282Y/p.C282Y) only requires treatment. We evaluated safety and feasibility of iron removal in healthy persons with elevated ferritin and HFE variants using blood donation procedures. Materials and

methods:

Thirty subjects with ferritin >200 ng/mL (women) or >300 ng/mL (men) with p.C282Y/p.C282Y, p.C282Y/p.H63D or p.H63D/p.H63D were randomized to weekly phlebotomy (removal of 450 mL whole blood) or erythrapheresis (removal of 360 mL red blood cells) every 14 days. The ferritin target was <100 ng/mL. A full blood count and ferritin were measured at each visit. Hemoglobin (Hb) ≥140 g/L was required at inclusion. If Hb dropped to <120 g/L (women) or <130 g/L (men), procedures were postponed (7 or 14 days). Primary endpoint was the number of procedures needed to the ferritin target; secondary objectives were duration of treatment and compliance. The treatment effect was tested with Poisson regression; number of procedures and treatment duration were compared between study arms with the Kruskal-Wallis test.

Results:

Twenty-five of 30 participants were men (83%); mean age was 47 years (SD 10.5), mean BMI 26.6 kg/m2 (SD 3.6); 17 had p.C282Y/p.C282Y, nine p.C282Y/p.H63D, four p.H63D/p.H63D. Median baseline Hb was 150 g/L (IQR 144, 1,559), median ferritin 504 ng/mL (IQR 406,620). Twenty-seven subjects completed the study. Treatment arm (p < 0.001) and HFE variant (p = 0.007) influenced the primary endpoint significantly. To ferritin levels <100 ng/mL, a median number of 7.5 (IQR 6.2, 9.8) phlebotomies and 4.0 (IQR 3.0, 5.8) erythraphereses (p = 0.001) was needed during a median of 66.5 days (IQR 49,103) and 78.5 days (IQR 46139), respectively (p = 0.448). Low Hb was the principal reason for protocol violation; anemia occurred in 13 participants (48%). Immediate complications were infrequent; fatigue was reported after 25% of phlebotomies and 45% of erythraphereses. Thirty-five procedures were postponed because of low Hb and 15 for non-medical reasons. The median interval was 7.0 (IQR 7.7) and 14.0 (IQR 14, 20) days between phlebotomies and erythraphereses, respectively.

Conclusion:

Blood donation procedures remove iron effectively in HC, but frequent treatments cause Hb decrease and fatigue that can impair feasibility.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2024 Tipo del documento: Article País de afiliación: Suiza

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2024 Tipo del documento: Article País de afiliación: Suiza