Monitoring of RBC rheology after cryopreservation to detect autologous blood doping in vivo? A pilot study.


Journal

Clinical hemorheology and microcirculation
ISSN: 1875-8622
Titre abrégé: Clin Hemorheol Microcirc
Pays: Netherlands
ID NLM: 9709206

Informations de publication

Date de publication:
2020
Historique:
pubmed: 18 7 2020
medline: 9 2 2021
entrez: 18 7 2020
Statut: ppublish

Résumé

Autologous blood doping (ABD) is applied to improve performance capacity. ABD includes blood donation, red blood cell (RBC) storage at -80°C and re-infusion prior to or during competition. ABD is not directly detectable with current detection techniques. Since cryopreservation is known to affect RBC physiology in vitro, the aim of the study was to examine whether these alterations are detectable in vivo. Blood from six healthy male donors was transferred into conventional blood bags, cryopreserved, stored for 18 weeks at -80°C and re-infused with a RBC volume corresponding to ∼4% of total blood volume into respective donor. RBC physiology parameters were measured before blood donation/re-infusion, and 0/1/2/6/24/48/72 h and 1 w post re-infusion. RBC parameters and age markers were unaffected during intervention. RBC deformability increased from pre-blood-sampling to pre-re-infusion while deformability and viscosity values remained unaltered post re-infusion. RBC nitric oxide associated analytes, metabolic parameters and electrolyte concentrations remained unaffected. The data of this pilot study indicate that the increase in RBC deformability might be related to neoformation of RBC after blood donation. The lack of changes in tested parameters might be related to the low re-infused RBC volume which might explain differences to in vitro results.

Sections du résumé

BACKGROUND BACKGROUND
Autologous blood doping (ABD) is applied to improve performance capacity. ABD includes blood donation, red blood cell (RBC) storage at -80°C and re-infusion prior to or during competition. ABD is not directly detectable with current detection techniques.
OBJECTIVE OBJECTIVE
Since cryopreservation is known to affect RBC physiology in vitro, the aim of the study was to examine whether these alterations are detectable in vivo.
METHODS METHODS
Blood from six healthy male donors was transferred into conventional blood bags, cryopreserved, stored for 18 weeks at -80°C and re-infused with a RBC volume corresponding to ∼4% of total blood volume into respective donor. RBC physiology parameters were measured before blood donation/re-infusion, and 0/1/2/6/24/48/72 h and 1 w post re-infusion.
RESULTS RESULTS
RBC parameters and age markers were unaffected during intervention. RBC deformability increased from pre-blood-sampling to pre-re-infusion while deformability and viscosity values remained unaltered post re-infusion. RBC nitric oxide associated analytes, metabolic parameters and electrolyte concentrations remained unaffected.
CONCLUSIONS CONCLUSIONS
The data of this pilot study indicate that the increase in RBC deformability might be related to neoformation of RBC after blood donation. The lack of changes in tested parameters might be related to the low re-infused RBC volume which might explain differences to in vitro results.

Identifiants

pubmed: 32675400
pii: CH200887
doi: 10.3233/CH-200887
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

367-379

Auteurs

Daniel A Bizjak (DA)

German Sport University Cologne, Department of Molecular and Cellular Sports Medicine, Cologne, Germany.

Andreas Grolle (A)

German Red Cross Blood Donation Service West, Hagen, Germany.

Javier Antonio Noriega Urena (JAN)

German Red Cross Blood Donation Service West, Hagen, Germany.

Wilhelm Bloch (W)

German Sport University Cologne, Department of Molecular and Cellular Sports Medicine, Cologne, Germany.

Robert Deitenbeck (R)

German Red Cross Blood Donation Service West, Hagen, Germany.

Marijke Grau (M)

German Sport University Cologne, Department of Molecular and Cellular Sports Medicine, Cologne, Germany.

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Classifications MeSH