TY - JOUR
T1 - Blood transcriptional signature of recombinant human erythropoietin administration and implications for antidoping strategies
AU - Durussel, Jérôme
AU - Haile, Diresibachew W.
AU - Mooses, Kerli
AU - Daskalaki, Evangelia
AU - Beattie, Wendy
AU - Mooses, Martin
AU - Mekonen, Wondyefraw
AU - Ongaro, Neford
AU - Anjila, Edwin
AU - Patel, Rajan K.
AU - Padmanabhan, Neal
AU - McBride, Martin W.
AU - McClure, John D.
AU - Pitsiladis, Yannis P.
N1 - Publisher Copyright:
© 2016 the American Physiological Society.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Recombinant human erythropoietin (rHuEPO) is frequently abused by athletes as a performance- enhancing drug, despite being prohibited by the World Anti- Doping Agency. Although the methods to detect blood doping, including rHuEPO injections, have improved in recent years, they remain imperfect. In a proof-of-principle study, we identified, replicated, and validated the whole blood transcriptional signature of rHuEPO in endurance-trained Caucasian males at sea level (n = 18) and Kenyan endurance runners at moderate altitude (n = 20), all of whom received rHuEPO injections for 4 wk. Transcriptional profiling shows that hundreds of transcripts were altered by rHuEPO in both cohorts. The main regulated expression pattern, observed in all participants, was characterized by a "rebound" effect with a profound upregulation during rHuEPO and a subsequent downregulation up to 4 wk postadministration. The functions of the identified genes were mainly related to the functional and structural properties of the red blood cell. Of the genes identified to be differentially expressed during and post-rHuEPO, we further confirmed a whole blood 34-transcript signature that can distinguish between samples collected pre-, during, and post-rHuEPO administration. By providing biomarkers that can reveal rHuEPO use, our findings represent an advance in the development of new methods for the detection of blood doping.
AB - Recombinant human erythropoietin (rHuEPO) is frequently abused by athletes as a performance- enhancing drug, despite being prohibited by the World Anti- Doping Agency. Although the methods to detect blood doping, including rHuEPO injections, have improved in recent years, they remain imperfect. In a proof-of-principle study, we identified, replicated, and validated the whole blood transcriptional signature of rHuEPO in endurance-trained Caucasian males at sea level (n = 18) and Kenyan endurance runners at moderate altitude (n = 20), all of whom received rHuEPO injections for 4 wk. Transcriptional profiling shows that hundreds of transcripts were altered by rHuEPO in both cohorts. The main regulated expression pattern, observed in all participants, was characterized by a "rebound" effect with a profound upregulation during rHuEPO and a subsequent downregulation up to 4 wk postadministration. The functions of the identified genes were mainly related to the functional and structural properties of the red blood cell. Of the genes identified to be differentially expressed during and post-rHuEPO, we further confirmed a whole blood 34-transcript signature that can distinguish between samples collected pre-, during, and post-rHuEPO administration. By providing biomarkers that can reveal rHuEPO use, our findings represent an advance in the development of new methods for the detection of blood doping.
KW - Blood doping
KW - Erythropoiesis
KW - MRNA
UR - http://www.scopus.com/inward/record.url?scp=84984843608&partnerID=8YFLogxK
U2 - 10.1152/physiolgenomics.00108.2015
DO - 10.1152/physiolgenomics.00108.2015
M3 - Journal article
C2 - 26757800
AN - SCOPUS:84984843608
SN - 1094-8341
VL - 48
SP - 202
EP - 209
JO - Physiological Genomics
JF - Physiological Genomics
IS - 3
ER -