AUTHOR=Reisz Julie A. , Tzounakas Vassilis L. , Nemkov Travis , Voulgaridou Artemis I. , Papassideri Issidora S. , Kriebardis Anastasios G. , D’Alessandro Angelo , Antonelou Marianna H. 

TITLE=Metabolic Linkage and Correlations to Storage Capacity in Erythrocytes from Glucose 6-Phosphate Dehydrogenase-Deficient Donors

JOURNAL=Frontiers in Medicine

VOLUME=Volume 4 - 2017

YEAR=2018

URL=https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2017.00248

DOI=10.3389/fmed.2017.00248

ISSN=2296-858X

ABSTRACT=Objective: In glucose 6-phosphate dehydrogenase (G6PD) deficiency, decreased NADPH regeneration in the pentose phosphate pathway and subnormal levels of reduced glutathione result in insufficient anti-oxidant defense, increased susceptibility of red blood cells (RBCs) to oxidative stress, and acute hemolysis following exposure to pro-oxidant drugs and infections. Despite the fact that redox disequilibrium is a prominent feature of RBC storage lesion it has been reported that the G6PD deficient RBCs store well, at least in respect to energy metabolism, but their overall metabolic phenotypes and molecular linkages to the storability profile are scarcely investigated.

Methods: We performed UHPLC-MS metabolomics analyses of weekly sampled RBC concentrates from G6PD sufficient and deficient donors, stored in CPD/SAGM from day 0 to storage day 42, followed by statistical and bioinformatics integration of the data.

Results: Other than previously reported alterations in glycolysis, metabolomics analyses revealed bioactive lipids, free fatty acids, bile acids, amino acids and purines as top variables discriminating RBC concentrates for G6PD deficient donors. Two-way ANOVA showed significant changes in the storage-dependent variation in fumarate, one carbon and sulfur metabolism, glutathione homeostasis and antioxidant defenses (including urate) components in G6PD deficient vs. sufficient donors. The levels of free fatty acids and their oxidized derivatives, as well as those of membrane-associated plasticizers were significantly lower in G6PD deficient units in comparison to controls. By using the strongest correlations between in vivo and ex vivo metabolic and physiological parameters, consecutively present throughout the storage period, several interactomes were produced that revealed an interesting interplay between redox, energy and hemolysis variables, that may be further associated with donor-specific differences in the post-transfusion performance of G6PD deficient RBCs. 

Conclusion: The metabolic phenotypes of G6PD deficient donors recapitulate the basic storage lesion profile that leads to loss of metabolic linkage and rewiring. Donor-related issues affect the storability of RBCs even in the narrow context of this donor subgroup in a way likely relevant to transfusion medicine.