Title

Longitudinal Profiling of Endogenous Steroids in Blood Using the Athlete Biological Passport Approach.

Authors

Equey, Tristan; Salamin, Olivier; Ponzetto, Federico; Nicoli, Raul; Kuuranne, Tiia; Saugy, Jonas; Saugy, Martial; Aikin, Reid; Baume, Norbert

Abstract

Context: Detection of endogenous anabolic androgenic steroids (EAAS), like testosterone (T), as doping agents has been improved with the launch of the Steroidal Module of the Athlete Biological Passport (ABP) in urine samples. Objective: To target doping practices with EAAS, particularly in individuals with low level of biomarkers excreted in urine, by including new target compounds measured in blood. Design: T and T/androstenedione (T/A4) distributions were obtained from 4 years of anti-doping data and applied as priors to analyze individual profiles from 2 T administration studies in female and male subjects. Setting: Anti-doping laboratory. Elite athletes (n = 823) and male and female clinical trials subjects (n = 19 and 14, respectively). Intervention(s): Two open-label administration studies were carried out. One involved a control phase period followed by patch and then oral T administration in male volunteers and the other followed female volunteers during 3 menstrual cycles with 28 days of daily transdermal T application during the second month. Main outcome measure(s): Serum samples were analyzed for T and A4 and the performance of a longitudinal ABP-based approach was evaluated for T and T/A4. Results: An ABP-based approach set at a 99% specificity flagged all female subjects during the transdermal T application period and 44% of subjects 3 days after the treatment. T showed the best sensitivity (74%) in response to transdermal T application in males. Conclusions: Inclusion of T and T/A4 as markers in the Steroidal Module can improve the performance of the ABP to identify T transdermal application, particularly in females.

Subjects

STEROIDS; ATHLETES

Publication

Journal of Clinical Endocrinology & Metabolism, 2023, Vol 108, Issue 8, p1937

ISSN

0021-972X

Publication type

Academic Journal

DOI

10.1210/clinem/dgad085