Volume 59, Issue 1 pp. 79-88
THE NHLBI RECIPIENT EPIDEMIOLOGY AND DONOR EVALUATION STUDY (REDS-III) RED BLOOD CELL OMICS (RBC-OMICS) STUDY

Intradonor reproducibility and changes in hemolytic variables during red blood cell storage: results of recall phase of the REDS-III RBC-Omics study

Marion C. Lanteri

Marion C. Lanteri

Vitalant Research Institute (previously Blood Systems Research Institute), University of San Francisco, San Francisco, California

Department of Laboratory Medicine, University of San Francisco, San Francisco, California

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Tamir Kanias

Tamir Kanias

Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, Atlanta, Georgia

Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Atlanta, Georgia

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Sheila Keating

Sheila Keating

Vitalant Research Institute (previously Blood Systems Research Institute), University of San Francisco, San Francisco, California

Department of Laboratory Medicine, University of San Francisco, San Francisco, California

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Mars Stone

Mars Stone

Vitalant Research Institute (previously Blood Systems Research Institute), University of San Francisco, San Francisco, California

Department of Laboratory Medicine, University of San Francisco, San Francisco, California

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Yuelong Guo

Yuelong Guo

RTI International, Atlanta, Georgia

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Grier P. Page

Grier P. Page

RTI International, Atlanta, Georgia

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Donald J. Brambilla

Donald J. Brambilla

RTI International, Rockville, Maryland

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Stacy M. Endres-Dighe

Stacy M. Endres-Dighe

RTI International, Rockville, Maryland

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Alan E. Mast

Alan E. Mast

Blood Research and Medical Sciences Institutes, Blood Center of Wisconsin, Milwaukee, Wisconsin

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Walter Bialkowski

Walter Bialkowski

Blood Research and Medical Sciences Institutes, Blood Center of Wisconsin, Milwaukee, Wisconsin

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Pam D'Andrea

Pam D'Andrea

The Institute for Transfusion Medicine, Pittsburgh, Pennsylvania

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Ritchard G. Cable

Ritchard G. Cable

American Red Cross, Farmington, Connecticut

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Bryan R. Spencer

Bryan R. Spencer

American Red Cross, Farmington, Connecticut

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Darrell J. Triulzi

Darrell J. Triulzi

The Institute for Transfusion Medicine, Pittsburgh, Pennsylvania

Department of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania

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Edward L. Murphy

Edward L. Murphy

Vitalant Research Institute (previously Blood Systems Research Institute), University of San Francisco, San Francisco, California

Department of Laboratory Medicine, University of San Francisco, San Francisco, California

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Steven Kleinman

Steven Kleinman

University of British Columbia, Victoria, British Columbia, Canada

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Mark T. Gladwin

Mark T. Gladwin

Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute, Atlanta, Georgia

Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Atlanta, Georgia

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Michael P. Busch

Corresponding Author

Michael P. Busch

Vitalant Research Institute (previously Blood Systems Research Institute), University of San Francisco, San Francisco, California

Department of Laboratory Medicine, University of San Francisco, San Francisco, California

Address reprint requests to: Michael P. Busch, MD, PhD, Blood Systems Research Institute, 270 Masonic Avenue, San Francisco, CA 94118; e-mail: [email protected]Search for more papers by this author
for the NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III Program

for the NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III Program

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First published: 08 November 2018
Citations: 47
The authors acknowledge NHLBI Recipient Epidemiology and Donor Evaluation Study-III (REDS-III), which was supported by NHLBI Contracts NHLBI HHSN2682011-00001I, -00002I, -00003I, -00004I, -00005I, -00006I, -00007I, -00008I, and -00009I.

The copyright line for this article was changed on June 13th 2019 after original online publication.

Abstract

BACKGROUND

Genetic determinants may underlie the susceptibility of red blood cells (RBCs) to hemolyze in vivo and during routine storage. This study characterized the reproducibility and dynamics of in vitro hemolysis variables from a subset of the 13,403 blood donors enrolled in the RBC-Omics study.

STUDY DESIGN AND METHODS

RBC-Omics donors with either low or high hemolysis results on 4°C-stored leukoreduced (LR)-RBC samples from enrollment donations stored for 39 to 42 days were recalled 2 to 12 months later to donate LR-RBCs. Samples of stored LR-RBCs from the unit and from transfer bags were evaluated for spontaneous and stress-induced hemolysis at selected storage time points. Intradonor reproducibility of hemolysis variables was evaluated in transfer bags over two donations. Hemolysis data at serial storage time points were generated on LR-RBCs from parent bags and analyzed by site, sex, race/ethnicity, and donation frequency.

RESULTS

A total of 664 donors were successfully recalled. Analysis of intradonor reproducibility revealed that osmotic and oxidative hemolysis demonstrated good and moderate reproducibility (Pearson's r = 0.85 and r = 0.53, respectively), while spontaneous hemolysis reproducibility was poor (r = 0.40). Longitudinal hemolysis in parent bags showed large increases over time in spontaneous (508.6%) and oxidative hemolysis (399.8%) and smaller increases in osmotic (9.4%) and mechanical fragility (3.4%; all p < 0.0001).

CONCLUSION

Spontaneous hemolysis is poorly reproducible in donors over time and may depend on site processing methods, while oxidative and osmotic hemolysis were reproducible in donors and hence could reflect consistent heritable phenotypes attributable to genetic traits. Spontaneous and oxidative hemolysis increased over time of storage, whereas osmotic and mechanical hemolysis remained relatively stable.

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