Frequent blood donations alter susceptibility of red blood cells to storage- and stress-induced hemolysis.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
01 2019
Historique:
received: 03 02 2018
revised: 14 05 2018
accepted: 27 05 2018
pubmed: 27 11 2018
medline: 7 5 2019
entrez: 27 11 2018
Statut: ppublish

Résumé

Frequent whole blood donations increase the prevalence of iron depletion in blood donors, which may subsequently interfere with normal erythropoiesis. The purpose of this study was to evaluate the associations between donation frequency and red blood cell (RBC) storage stability in a racially/ethnically diverse population of blood donors. Leukoreduced RBC concentrate-derived samples from 13,403 donors were stored for 39 to 42 days (1-6°C) and then evaluated for storage, osmotic, and oxidative hemolysis. Iron status was evaluated by plasma ferritin measurement and self-reported intake of iron supplements. Donation history in the prior 2 years was obtained for each subject. Frequent blood donors enrolled in this study were likely to be white, male, and of older age (56.1 ± 5.0 years). Prior donation intensity was negatively associated with oxidative hemolysis (p < 0.0001) in multivariate analyses correcting for age, sex, and race/ethnicity. Increased plasma ferritin concentration was associated with increased RBC susceptibility to each of the three measures of hemolysis (p < 0.0001 for all), whereas self-reported iron intake was associated with reduced susceptibility to osmotic and oxidative hemolysis (p < 0.0001 for both). Frequent blood donations may alter the quality of blood components by modulating RBC predisposition to hemolysis. RBCs collected from frequent donors with low ferritin have altered susceptibility to hemolysis. Thus, frequent donation and associated iron loss may alter the quality of stored RBC components collected from iron-deficient donors. Further investigation is necessary to assess posttransfusion safety and efficacy in patients receiving these RBC products.

Sections du résumé

BACKGROUND
Frequent whole blood donations increase the prevalence of iron depletion in blood donors, which may subsequently interfere with normal erythropoiesis. The purpose of this study was to evaluate the associations between donation frequency and red blood cell (RBC) storage stability in a racially/ethnically diverse population of blood donors.
STUDY DESIGN
Leukoreduced RBC concentrate-derived samples from 13,403 donors were stored for 39 to 42 days (1-6°C) and then evaluated for storage, osmotic, and oxidative hemolysis. Iron status was evaluated by plasma ferritin measurement and self-reported intake of iron supplements. Donation history in the prior 2 years was obtained for each subject.
RESULTS
Frequent blood donors enrolled in this study were likely to be white, male, and of older age (56.1 ± 5.0 years). Prior donation intensity was negatively associated with oxidative hemolysis (p < 0.0001) in multivariate analyses correcting for age, sex, and race/ethnicity. Increased plasma ferritin concentration was associated with increased RBC susceptibility to each of the three measures of hemolysis (p < 0.0001 for all), whereas self-reported iron intake was associated with reduced susceptibility to osmotic and oxidative hemolysis (p < 0.0001 for both).
CONCLUSIONS
Frequent blood donations may alter the quality of blood components by modulating RBC predisposition to hemolysis. RBCs collected from frequent donors with low ferritin have altered susceptibility to hemolysis. Thus, frequent donation and associated iron loss may alter the quality of stored RBC components collected from iron-deficient donors. Further investigation is necessary to assess posttransfusion safety and efficacy in patients receiving these RBC products.

Identifiants

pubmed: 30474858
doi: 10.1111/trf.14998
pmc: PMC6347021
mid: NIHMS993156
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

67-78

Subventions

Organisme : NHLBI NIH HHS
ID : HHSN268201100001I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100004I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100008I
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL098032
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100005I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100007I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100002I
Pays : United States
Organisme : OLAO NIH HHS
ID : HHSN263201000009I
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2018 AABB.

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Auteurs

Tamir Kanias (T)

Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Mars Stone (M)

Blood Systems Research Institute, San Francisco, and Department of Laboratory Medicine, University of California, San Francisco, California.

Grier P Page (GP)

RTI International, Atlanta, Georgia.

Yuelong Guo (Y)

RTI International, Research Triangle Park, North Carolina.

Stacy M Endres-Dighe (SM)

RTI International, Rockville, Maryland.

Marion C Lanteri (MC)

Blood Systems Research Institute, San Francisco, and Department of Laboratory Medicine, University of California, San Francisco, California.

Bryan R Spencer (BR)

American Red Cross Blood Services, Dedham, Massachusetts.

Ritchard G Cable (RG)

American Red Cross, Farmington, Connecticut.

Darrell J Triulzi (DJ)

Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania.
The Institute for Transfusion Medicine, Pittsburgh, Pennsylvania.

Joseph E Kiss (JE)

The Institute for Transfusion Medicine, Pittsburgh, Pennsylvania.

Edward L Murphy (EL)

Blood Systems Research Institute, San Francisco, and Department of Laboratory Medicine, University of California, San Francisco, California.

Steve Kleinman (S)

University of British Columbia, Victoria, British Columbia, Canada.

Mark T Gladwin (MT)

Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, Pennsylvania.
Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

Michael P Busch (MP)

Blood Systems Research Institute, San Francisco, and Department of Laboratory Medicine, University of California, San Francisco, California.

Alan E Mast (AE)

Blood Research Institute, Blood Center of Wisconsin, and Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee.

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