Red Blood Cell Storage: From Genome to Exposome Towards Personalized Transfusion Medicine

被引:12
作者
D'Alessandro, Angelo [1 ]
Hod, Eldad A. [2 ]
机构
[1] Univ Colorado, Dept Biochem & Mol Genet, Anschutz Med Campus,12801 East 17th Ave L18-9118, Aurora, CO 80045 USA
[2] Columbia Univ, Irving Med Ctr, Dept Pathol & Cell Biol, New York, NY USA
关键词
Precision transfusion medicine; Omics; Big data; Erythrocyte; Storage lesion; METABOLISM; SEX; AGE; HERITABILITY; HEMOLYSIS; RECOVERY; STRESS; UPDATE; DONORS; TIME;
D O I
10.1016/j.tmrv.2023.150750
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the last decade, the introduction of omics technologies-especially high-throughput genomics and metabolomics-has contributed significantly to our understanding of the role of donor genetics and nongenetic determinants of red blood cell storage biology. Here we briefly review the main advances in these areas, to the extent these contributed to the appreciation of the impact of donor sex, age, ethnicity, but also processing strategies and donor environmental, dietary or other exposures - the so-called exposome-to the onset and severity of the storage lesion. We review recent advances on the role of genetically encoded polymorphisms on red cell storage biology, and relate these findings with parameters of storage quality and post-transfusion efficacy, such as hemolysis, post-transfusion intra- and extravascular hemolysis and hemoglobin increments. Finally, we suggest that the combination of these novel technologies have the potential to drive further developments towards personalized (or precision) transfusion medicine approaches.
引用
收藏
页数:5
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