Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion

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Standard

Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion. / Andersen, Andreas Breenfeldt; Bejder, Jacob; Bonne, Thomas Christian; Sørensen, Henrik; Sørensen, Helle; Jung, Grace; Ganz, Tomas; Nemeth, Elizabeta; Secher, Niels H; Johansson, Pär I; Nordsborg, Nikolai Baastrup.

I: Medicine and Science in Sports and Exercise, Bind 54, Nr. 9, 2022, s. 1604-1616.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Andersen, AB, Bejder, J, Bonne, TC, Sørensen, H, Sørensen, H, Jung, G, Ganz, T, Nemeth, E, Secher, NH, Johansson, PI & Nordsborg, NB 2022, 'Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion', Medicine and Science in Sports and Exercise, bind 54, nr. 9, s. 1604-1616. https://doi.org/10.1249/MSS.0000000000002950

APA

Andersen, A. B., Bejder, J., Bonne, T. C., Sørensen, H., Sørensen, H., Jung, G., Ganz, T., Nemeth, E., Secher, N. H., Johansson, P. I., & Nordsborg, N. B. (2022). Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion. Medicine and Science in Sports and Exercise, 54(9), 1604-1616. https://doi.org/10.1249/MSS.0000000000002950

Vancouver

Andersen AB, Bejder J, Bonne TC, Sørensen H, Sørensen H, Jung G o.a. Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion. Medicine and Science in Sports and Exercise. 2022;54(9):1604-1616. https://doi.org/10.1249/MSS.0000000000002950

Author

Andersen, Andreas Breenfeldt ; Bejder, Jacob ; Bonne, Thomas Christian ; Sørensen, Henrik ; Sørensen, Helle ; Jung, Grace ; Ganz, Tomas ; Nemeth, Elizabeta ; Secher, Niels H ; Johansson, Pär I ; Nordsborg, Nikolai Baastrup. / Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion. I: Medicine and Science in Sports and Exercise. 2022 ; Bind 54, Nr. 9. s. 1604-1616.

Bibtex

@article{f7cc6b0eb45f4cc192a60dc101afa736,
title = "Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion",
abstract = "Purpose: We investigated whether hepcidin and erythroferrone (ERFE) could complement the Athlete Biological Passport (ABP) in indirectly detecting a 130 mL packed red blood cells (RBCs) autologous blood transfusion. Endurance performance was evaluated.Methods: Forty-eight healthy men (n = 24) and women (n = 24) participated. Baseline samples were collected weekly followed by randomization to a blood transfusion (BT, n = 24) or control group (CON, n = 24). Only the BT group donated 450 mL whole blood from which 130 mL RBCs was reinfused four weeks later. Blood samples were collected 3, 7, 14, 21 and 28 days after donation, and 3, 6, and 24 hours and 2, 3, and 6 days following reinfusion. In the CON group samples were collected with the same frequency. Endurance performance was evaluated by a 650-kCal time trial (n = 13) before and one and six days after reinfusion.Results: A time×treatment effect existed (P < 0.05) for hepcidin and ERFE. Hepcidin was increased (P < 0.01) ~110 and 89% six and 24 hours after reinfusion. Using an individual approach (99% specificity, e.g. allowing 1:100 false-positive), sensitivities, i.e. true positives, of 30% and 61% was found for hepcidin and ERFE, respectively. For the ABP, the most sensitive marker was Off-hr score ([Hb] (g·L-1) - 60 × √RET%) (P < 0.05) with a maximal sensitivity of ~58% and ~ 9% following donation and reinfusion, respectively. Combining the findings for hepcidin, ERFE and the ABP yielded a sensitivity across all time-points of 83% following reinfusion in BT. Endurance performance increased 24 hours (+6.4%, P < 0.01) and six days following reinfusion (+5.8%, P < 0.01).Conclusions: Hepcidin and ERFE may serve as biomarkers in an anti-doping context following an ergogenic, small-volume blood transfusion.",
keywords = "Faculty of Science, Transfusion, Biomarker, Anti-doping, Sex-specific, Micro-dosing, Hepcidin, Erythroferrone, Athlete Biological Passport",
author = "Andersen, {Andreas Breenfeldt} and Jacob Bejder and Bonne, {Thomas Christian} and Henrik S{\o}rensen and Helle S{\o}rensen and Grace Jung and Tomas Ganz and Elizabeta Nemeth and Secher, {Niels H} and Johansson, {P{\"a}r I} and Nordsborg, {Nikolai Baastrup}",
note = "Copyright {\textcopyright} 2022 by the American College of Sports Medicine.",
year = "2022",
doi = "10.1249/MSS.0000000000002950",
language = "English",
volume = "54",
pages = "1604--1616",
journal = "Medicine and Science in Sports and Exercise",
issn = "0195-9131",
publisher = "Lippincott Williams & Wilkins",
number = "9",

}

RIS

TY - JOUR

T1 - Hepcidin and erythroferrone complement the Athlete Biological Passport in the detection of autologous blood transfusion

AU - Andersen, Andreas Breenfeldt

AU - Bejder, Jacob

AU - Bonne, Thomas Christian

AU - Sørensen, Henrik

AU - Sørensen, Helle

AU - Jung, Grace

AU - Ganz, Tomas

AU - Nemeth, Elizabeta

AU - Secher, Niels H

AU - Johansson, Pär I

AU - Nordsborg, Nikolai Baastrup

N1 - Copyright © 2022 by the American College of Sports Medicine.

PY - 2022

Y1 - 2022

N2 - Purpose: We investigated whether hepcidin and erythroferrone (ERFE) could complement the Athlete Biological Passport (ABP) in indirectly detecting a 130 mL packed red blood cells (RBCs) autologous blood transfusion. Endurance performance was evaluated.Methods: Forty-eight healthy men (n = 24) and women (n = 24) participated. Baseline samples were collected weekly followed by randomization to a blood transfusion (BT, n = 24) or control group (CON, n = 24). Only the BT group donated 450 mL whole blood from which 130 mL RBCs was reinfused four weeks later. Blood samples were collected 3, 7, 14, 21 and 28 days after donation, and 3, 6, and 24 hours and 2, 3, and 6 days following reinfusion. In the CON group samples were collected with the same frequency. Endurance performance was evaluated by a 650-kCal time trial (n = 13) before and one and six days after reinfusion.Results: A time×treatment effect existed (P < 0.05) for hepcidin and ERFE. Hepcidin was increased (P < 0.01) ~110 and 89% six and 24 hours after reinfusion. Using an individual approach (99% specificity, e.g. allowing 1:100 false-positive), sensitivities, i.e. true positives, of 30% and 61% was found for hepcidin and ERFE, respectively. For the ABP, the most sensitive marker was Off-hr score ([Hb] (g·L-1) - 60 × √RET%) (P < 0.05) with a maximal sensitivity of ~58% and ~ 9% following donation and reinfusion, respectively. Combining the findings for hepcidin, ERFE and the ABP yielded a sensitivity across all time-points of 83% following reinfusion in BT. Endurance performance increased 24 hours (+6.4%, P < 0.01) and six days following reinfusion (+5.8%, P < 0.01).Conclusions: Hepcidin and ERFE may serve as biomarkers in an anti-doping context following an ergogenic, small-volume blood transfusion.

AB - Purpose: We investigated whether hepcidin and erythroferrone (ERFE) could complement the Athlete Biological Passport (ABP) in indirectly detecting a 130 mL packed red blood cells (RBCs) autologous blood transfusion. Endurance performance was evaluated.Methods: Forty-eight healthy men (n = 24) and women (n = 24) participated. Baseline samples were collected weekly followed by randomization to a blood transfusion (BT, n = 24) or control group (CON, n = 24). Only the BT group donated 450 mL whole blood from which 130 mL RBCs was reinfused four weeks later. Blood samples were collected 3, 7, 14, 21 and 28 days after donation, and 3, 6, and 24 hours and 2, 3, and 6 days following reinfusion. In the CON group samples were collected with the same frequency. Endurance performance was evaluated by a 650-kCal time trial (n = 13) before and one and six days after reinfusion.Results: A time×treatment effect existed (P < 0.05) for hepcidin and ERFE. Hepcidin was increased (P < 0.01) ~110 and 89% six and 24 hours after reinfusion. Using an individual approach (99% specificity, e.g. allowing 1:100 false-positive), sensitivities, i.e. true positives, of 30% and 61% was found for hepcidin and ERFE, respectively. For the ABP, the most sensitive marker was Off-hr score ([Hb] (g·L-1) - 60 × √RET%) (P < 0.05) with a maximal sensitivity of ~58% and ~ 9% following donation and reinfusion, respectively. Combining the findings for hepcidin, ERFE and the ABP yielded a sensitivity across all time-points of 83% following reinfusion in BT. Endurance performance increased 24 hours (+6.4%, P < 0.01) and six days following reinfusion (+5.8%, P < 0.01).Conclusions: Hepcidin and ERFE may serve as biomarkers in an anti-doping context following an ergogenic, small-volume blood transfusion.

KW - Faculty of Science

KW - Transfusion

KW - Biomarker

KW - Anti-doping

KW - Sex-specific

KW - Micro-dosing

KW - Hepcidin

KW - Erythroferrone

KW - Athlete Biological Passport

U2 - 10.1249/MSS.0000000000002950

DO - 10.1249/MSS.0000000000002950

M3 - Journal article

C2 - 35482790

VL - 54

SP - 1604

EP - 1616

JO - Medicine and Science in Sports and Exercise

JF - Medicine and Science in Sports and Exercise

SN - 0195-9131

IS - 9

ER -

ID: 304749145