A randomized trial of blood donor iron repletion on red cell quality for transfusion and donor cognition and well-being

Author:

Hod Eldad A.1ORCID,Brittenham Gary M.23,Bitan Zachary C.1,Feit Yona1,Gaelen Jordan I.1,La Carpia Francesca1ORCID,Sandoval Luke A.1ORCID,Zhou Alice T.1,Soffing Mark4,Mintz Akiva4,Schwartz Joseph1,Eng Connie5,Scotto Marta5,Caccappolo Elise6,Habeck Christian6,Stern Yaakov6,McMahon Donald J.3ORCID,Kessler Debra A.7,Shaz Beth H.7ORCID,Francis Richard O.1,Spitalnik Steven L.1ORCID

Affiliation:

1. 1Department of Pathology and Cell Biology, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

2. 2Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

3. 3Department of Medicine, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

4. 4Department of Nuclear Medicine, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

5. 5Department of Pharmacy, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

6. 6Department of Neurology, Division of Cognitive Neuroscience, Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital, New York, NY

7. 7New York Blood Center, New York, NY

Abstract

Abstract Although altruistic regular blood donors are vital for the blood supply, many become iron deficient from donation-induced iron loss. The effects of blood donation–induced iron deficiency on red cell transfusion quality or donor cognition are unknown. In this double-blind, randomized trial, adult iron-deficient blood donors (n = 79; ferritin < 15 μg/L and zinc protoporphyrin >60 μMol/mol heme) who met donation qualifications were enrolled. A first standard blood donation was followed by the gold-standard measure for red cell storage quality: a 51-chromium posttransfusion red cell recovery study. Donors were then randomized to intravenous iron repletion (1 g low-molecular-weight iron dextran) or placebo. A second donation ∼5 months later was followed by another recovery study. Primary outcome was the within-subject change in posttransfusion recovery. The primary outcome measure of an ancillary study reported here was the National Institutes of Health Toolbox–derived uncorrected standard Cognition Fluid Composite Score. Overall, 983 donors were screened; 110 were iron-deficient, and of these, 39 were randomized to iron repletion and 40 to placebo. Red cell storage quality was unchanged by iron repletion: mean change in posttransfusion recovery was 1.6% (95% confidence interval −0.5 to 3.8) and −0.4% (−2.0 to 1.2) with and without iron, respectively. Iron repletion did not affect any cognition or well-being measures. These data provide evidence that current criteria for blood donation preserve red cell transfusion quality for the recipient and protect adult donors from measurable effects of blood donation–induced iron deficiency on cognition. This trial was registered at www.clinicaltrials.gov as NCT02889133 and NCT02990559.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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