Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men

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Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men. / Bejder, Jacob; Robach, Paul; Lundby, Anne-Kristine; Cornu, Catherine; Sallet, Pierre; Cairo, Gaetano; Lundby, Carsten.

I: Drug Testing and Analysis, Bind 12, Nr. 7, 2020, s. 975-979.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bejder, J, Robach, P, Lundby, A-K, Cornu, C, Sallet, P, Cairo, G & Lundby, C 2020, 'Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men', Drug Testing and Analysis, bind 12, nr. 7, s. 975-979. https://doi.org/10.1002/dta.2795

APA

Bejder, J., Robach, P., Lundby, A-K., Cornu, C., Sallet, P., Cairo, G., & Lundby, C. (2020). Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men. Drug Testing and Analysis, 12(7), 975-979. https://doi.org/10.1002/dta.2795

Vancouver

Bejder J, Robach P, Lundby A-K, Cornu C, Sallet P, Cairo G o.a. Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men. Drug Testing and Analysis. 2020;12(7):975-979. https://doi.org/10.1002/dta.2795

Author

Bejder, Jacob ; Robach, Paul ; Lundby, Anne-Kristine ; Cornu, Catherine ; Sallet, Pierre ; Cairo, Gaetano ; Lundby, Carsten. / Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men. I: Drug Testing and Analysis. 2020 ; Bind 12, Nr. 7. s. 975-979.

Bibtex

@article{66b300f5dabb4a648a96fec689eec3df,
title = "Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men",
abstract = "Recombinant human erythropoietin (rhEpo) can improve human performance, but misuse remains difficult to detect. C-terminal fibroblast growth factor 23 (cFGF23) was recently demonstrated to increase following injection of a single high dose rhEpo, but the effect of more frequent low doses is unknown. Using a randomized double-blind placebo-controlled design, we investigated whether 2 weeks of subcutaneous injections three times a week of 50 IU/kg Eprex (low-dose) or 20 IU/kg Eprex (micro-dose) increase cFGF23 levels compared with saline (placebo) injections in 24 healthy males. Venous blood was sampled at day -3, 0, 1, 3, 11, 14, 18, and 25 of the treatment and analyzed for cFGF23 and erythropoietin concentration ([EPO]). The level of cFGF23 was similar at days -3, 0, 1, 3, 11, 14, 18, and 25 with the low-dose (23 ± 4, 26 ± 5, 23 ± 7, 27 ± 6, 25 ± 8, 24 ± 10, 22 ± 5, and 24 ± 7 RU/mL, respectively), micro-dose (23 ± 6, 25 ± 5, 23 ± 8, 28 ± 9, 27 ± 7, 25 ± 9, 25 ± 5, and 23 ± 6 RU/mL, respectively) and placebo (23 ± 6, 24 ± 6, 26 ± 7, 26 ± 6, 31 ± 6, 31 ± 7, 24 ± 4, and 27 ± 8 RU/mL, respectively) treatment. The correlation coefficient between plasma [EPO] and plasma cFGF23 levels was R2 = 0.01 and insignificant. The results demonstrate that cFGF23 is not sensitive to low doses of subcutaneous rhEpo injections in healthy males.",
keywords = "Faculty of Science, Biomarker discovery, Doping, Erythropoiesis",
author = "Jacob Bejder and Paul Robach and Anne-Kristine Lundby and Catherine Cornu and Pierre Sallet and Gaetano Cairo and Carsten Lundby",
note = "{\textcopyright} 2020 John Wiley & Sons, Ltd.",
year = "2020",
doi = "10.1002/dta.2795",
language = "English",
volume = "12",
pages = "975--979",
journal = "Drug Testing and Analysis",
issn = "1942-7603",
publisher = "JohnWiley & Sons Ltd",
number = "7",

}

RIS

TY - JOUR

T1 - Low doses of recombinant human erythropoietin does not affect C-terminal FGF23 in healthy men

AU - Bejder, Jacob

AU - Robach, Paul

AU - Lundby, Anne-Kristine

AU - Cornu, Catherine

AU - Sallet, Pierre

AU - Cairo, Gaetano

AU - Lundby, Carsten

N1 - © 2020 John Wiley & Sons, Ltd.

PY - 2020

Y1 - 2020

N2 - Recombinant human erythropoietin (rhEpo) can improve human performance, but misuse remains difficult to detect. C-terminal fibroblast growth factor 23 (cFGF23) was recently demonstrated to increase following injection of a single high dose rhEpo, but the effect of more frequent low doses is unknown. Using a randomized double-blind placebo-controlled design, we investigated whether 2 weeks of subcutaneous injections three times a week of 50 IU/kg Eprex (low-dose) or 20 IU/kg Eprex (micro-dose) increase cFGF23 levels compared with saline (placebo) injections in 24 healthy males. Venous blood was sampled at day -3, 0, 1, 3, 11, 14, 18, and 25 of the treatment and analyzed for cFGF23 and erythropoietin concentration ([EPO]). The level of cFGF23 was similar at days -3, 0, 1, 3, 11, 14, 18, and 25 with the low-dose (23 ± 4, 26 ± 5, 23 ± 7, 27 ± 6, 25 ± 8, 24 ± 10, 22 ± 5, and 24 ± 7 RU/mL, respectively), micro-dose (23 ± 6, 25 ± 5, 23 ± 8, 28 ± 9, 27 ± 7, 25 ± 9, 25 ± 5, and 23 ± 6 RU/mL, respectively) and placebo (23 ± 6, 24 ± 6, 26 ± 7, 26 ± 6, 31 ± 6, 31 ± 7, 24 ± 4, and 27 ± 8 RU/mL, respectively) treatment. The correlation coefficient between plasma [EPO] and plasma cFGF23 levels was R2 = 0.01 and insignificant. The results demonstrate that cFGF23 is not sensitive to low doses of subcutaneous rhEpo injections in healthy males.

AB - Recombinant human erythropoietin (rhEpo) can improve human performance, but misuse remains difficult to detect. C-terminal fibroblast growth factor 23 (cFGF23) was recently demonstrated to increase following injection of a single high dose rhEpo, but the effect of more frequent low doses is unknown. Using a randomized double-blind placebo-controlled design, we investigated whether 2 weeks of subcutaneous injections three times a week of 50 IU/kg Eprex (low-dose) or 20 IU/kg Eprex (micro-dose) increase cFGF23 levels compared with saline (placebo) injections in 24 healthy males. Venous blood was sampled at day -3, 0, 1, 3, 11, 14, 18, and 25 of the treatment and analyzed for cFGF23 and erythropoietin concentration ([EPO]). The level of cFGF23 was similar at days -3, 0, 1, 3, 11, 14, 18, and 25 with the low-dose (23 ± 4, 26 ± 5, 23 ± 7, 27 ± 6, 25 ± 8, 24 ± 10, 22 ± 5, and 24 ± 7 RU/mL, respectively), micro-dose (23 ± 6, 25 ± 5, 23 ± 8, 28 ± 9, 27 ± 7, 25 ± 9, 25 ± 5, and 23 ± 6 RU/mL, respectively) and placebo (23 ± 6, 24 ± 6, 26 ± 7, 26 ± 6, 31 ± 6, 31 ± 7, 24 ± 4, and 27 ± 8 RU/mL, respectively) treatment. The correlation coefficient between plasma [EPO] and plasma cFGF23 levels was R2 = 0.01 and insignificant. The results demonstrate that cFGF23 is not sensitive to low doses of subcutaneous rhEpo injections in healthy males.

KW - Faculty of Science

KW - Biomarker discovery

KW - Doping

KW - Erythropoiesis

U2 - 10.1002/dta.2795

DO - 10.1002/dta.2795

M3 - Journal article

C2 - 32216032

VL - 12

SP - 975

EP - 979

JO - Drug Testing and Analysis

JF - Drug Testing and Analysis

SN - 1942-7603

IS - 7

ER -

ID: 240981770