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Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients.

Publication ,  Journal Article
Gehrke, S; Shah, N; Gamboni, F; Kamyszek, R; Srinivasan, AJ; Gray, A; Landrigan, M; Welsby, I; D'Alessandro, A
Published in: Transfusion
October 2019

BACKGROUND: Red blood cell exchange (RCE) transfusions are a mainstay in the treatment of sickle cell anemia (SCA), and allow a temporary restoration of physiological parameters with respect to erythrocyte oxygen carrying capacity and systems metabolism. Recently, we noted that 1) RCE significantly impacts recipients' metabolism in SCA; 2) fresh and end-of-storage red blood cell (RBC) units differently impact systems of metabolism in healthy autologous recipients; and 3) phosphate/inosine/pyruvate/adenine (PIPA) solution reverses the metabolic age of stored RBCs. Therefore, we hypothesized that RCE with PIPA-treated RBC units could further increase the metabolic benefits of RCE in SCA patients. STUDY DESIGN AND METHODS: Circulating plasma and erythrocytes were collected from patients with SCA before and after RCE, with either conventional or PIPA-treated RBC units, prior to metabolomics analyses. RESULTS: Consistent with prior work, RCE significantly decreased circulating levels of markers of systemic hypoxemia (lactate, succinate) and decreased plasma levels of acyl-carnitines and amino acids. However, PIPA-treated exchanges were superior to untreated RCEs, with a higher energy state and an increased capacity to activate the pentose phosphate pathway and glutamine metabolism. In addition, RBCs and plasma from recipients of PIPA-treated RBC units resulted in significantly decreased levels of post-transfusion plasticizers, though at the expense of higher circulating levels of oxidized purines (hypoxanthine, xanthine, and the antioxidant urate). CONCLUSION: Transfusion of PIPA-treated RBCs further increases the metabolic benefits of RCE to patients with SCA, significantly reducing the levels of post-transfusion plasticizers.

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Published In

Transfusion

DOI

EISSN

1537-2995

Publication Date

October 2019

Volume

59

Issue

10

Start / End Page

3102 / 3112

Location

United States

Related Subject Headings

  • Purines
  • Plasticizers
  • Pentose Phosphate Pathway
  • Metabolomics
  • Male
  • Humans
  • Exchange Transfusion, Whole Blood
  • Erythrocytes
  • Erythrocyte Transfusion
  • Cardiovascular System & Hematology
 

Citation

APA
Chicago
ICMJE
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Gehrke, S., Shah, N., Gamboni, F., Kamyszek, R., Srinivasan, A. J., Gray, A., … D’Alessandro, A. (2019). Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients. Transfusion, 59(10), 3102–3112. https://doi.org/10.1111/trf.15467
Gehrke, Sarah, Nirmish Shah, Fabia Gamboni, Reed Kamyszek, Amudan J. Srinivasan, Alan Gray, Matthew Landrigan, Ian Welsby, and Angelo D’Alessandro. “Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients.Transfusion 59, no. 10 (October 2019): 3102–12. https://doi.org/10.1111/trf.15467.
Gehrke S, Shah N, Gamboni F, Kamyszek R, Srinivasan AJ, Gray A, et al. Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients. Transfusion. 2019 Oct;59(10):3102–12.
Gehrke, Sarah, et al. “Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients.Transfusion, vol. 59, no. 10, Oct. 2019, pp. 3102–12. Pubmed, doi:10.1111/trf.15467.
Gehrke S, Shah N, Gamboni F, Kamyszek R, Srinivasan AJ, Gray A, Landrigan M, Welsby I, D’Alessandro A. Metabolic impact of red blood cell exchange with rejuvenated red blood cells in sickle cell patients. Transfusion. 2019 Oct;59(10):3102–3112.
Journal cover image

Published In

Transfusion

DOI

EISSN

1537-2995

Publication Date

October 2019

Volume

59

Issue

10

Start / End Page

3102 / 3112

Location

United States

Related Subject Headings

  • Purines
  • Plasticizers
  • Pentose Phosphate Pathway
  • Metabolomics
  • Male
  • Humans
  • Exchange Transfusion, Whole Blood
  • Erythrocytes
  • Erythrocyte Transfusion
  • Cardiovascular System & Hematology