Interest of hair tests to discriminate a tail end of a doping regimen from a possible unpredictable source of a prohibited substance in case of challenging an anti-doping rule violation
Abstract
The presence of letrozole, an aromatase inhibitor, in an athlete’s sample constitutes one of the more frequent anti-doping rules violation. It is possible to challenge this violation but it is the athletes who have to demonstrate their innocence. The conditions to evidence/establish the absence of fault or negligence hinge on two points: 1. the athletes or their legal representatives have to present verified circumstances of contamination and the source of contamination has to be identified; and 2. there have to be verified claims by the athlete about the fact that the intake of the prohibited substance was not known, i.e. that the violation was not intentional. This corresponds to the suggested shift terminology from “contaminated product” to “unpredictable source of a prohibited substance”. In the recent years, several top athletes challenged their ADRV with a low urine letrozole concentration and requested a hair test. In three cases, letrozole concentration in segmented hair, particularly in the segment corresponding to the urine AAF was significantly lower than 1 pg/mg, which is the limit of quantification of the method. Considering that a ¼ of a 2.5 mg therapeutic dose of letrozole produces a hair concentration of approximately 30 pg/mg, it is easy to establish that the dose that entered in the body of these athletes was incidental. Nevertheless, all three athletes were sentenced a 2-years ban as the source of contamination was not identified. In that sense, the WADA dogma contradicts scientific evidence, and from a forensic perspective, this appears difficult to understand.
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Research ethics: Not applicable.
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Informed consent: Not applicable.
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Author contributions: The author has accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The author states no conflict of interest.
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Research funding: None declared.
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Data availability: Not applicable.
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Articles in the same Issue
- Frontmatter
- Editorials
- The Friedewald formula strikes back
- Liquid biopsy in oncology: navigating technical hurdles and future transition for precision medicine
- The neglected issue of pyridoxal- 5′ phosphate
- Reviews
- Health literacy: a new challenge for laboratory medicine
- Clinical applications of circulating tumor cell detection: challenges and strategies
- Opinion Papers
- Pleural effusion as a sample matrix for laboratory analyses in cancer management: a perspective
- Interest of hair tests to discriminate a tail end of a doping regimen from a possible unpredictable source of a prohibited substance in case of challenging an anti-doping rule violation
- Perspectives
- Sigma Metrics misconceptions and limitations
- EN ISO 15189 revision: EFLM Committee Accreditation and ISO/CEN standards (C: A/ISO) analysis and general remarks on the changes
- General Clinical Chemistry and Laboratory Medicine
- Evaluation of current indirect methods for measuring LDL-cholesterol
- Verification of automated review, release and reporting of results with assessment of the risk of harm for patients: the procedure algorithm proposal for clinical laboratories
- Progranulin measurement with a new automated method: a step forward in the diagnostic approach to neurodegenerative disorders
- A comparative analysis of current С-peptide assays compared to a reference method: can we overcome inertia to standardization?
- Blood samples for ammonia analysis do not require transport to the laboratory on ice: a study of ammonia stability and cause of in vitro ammonia increase in samples from patients with hyperammonaemia
- A physio-chemical mathematical model of the effects of blood analysis delay on acid-base, metabolite and electrolyte status: evaluation in blood from critical care patients
- Evolution of autoimmune diagnostics over the past 10 years: lessons learned from the UK NEQAS external quality assessment EQA programs
- Comparison between monotest and traditional batch-based ELISA assays for therapeutic drug monitoring of infliximab and adalimumab levels and anti-drug antibodies
- Evaluation of pre-analytical factors impacting urine test strip and chemistry results
- Evaluation of AUTION EYE AI-4510 flow cell morphology analyzer for counting particles in urine
- Reference Values and Biological Variations
- Estimation of the allowable total error of the absolute CD34+ cell count by flow cytometry using data from UK NEQAS exercises 2004–2024
- Establishment of gender– and age–related reference intervals for serum uric acid in adults based on big data from Zhejiang Province in China
- Cancer Diagnostics
- Tumor specific protein 70 targeted tumor cell isolation technology can improve the accuracy of cytopathological examination
- Cardiovascular Diseases
- Diagnostic performance of Mindray CL1200i high sensitivity cardiac troponin I assay compared to Abbott Alinity cardiac troponin I assay for the diagnosis of type 1 and 2 acute myocardial infarction in females and males: MERITnI study
- Infectious Diseases
- Evidence-based assessment of the application of Six Sigma to infectious disease serology quality control
- Letters to the Editor
- Evaluating the accuracy of ChatGPT in classifying normal and abnormal blood cell morphology
- Refining within-subject biological variation estimation using routine laboratory data: practical applications of the refineR algorithm
- Early rule-out high-sensitivity troponin protocols require continuous analytical robustness: a caution regarding the potential for troponin assay down-calibration
- Biochemical evidence of vitamin B12 deficiency: a crucial issue to address supplementation in pregnant women
- Plasmacytoid dendritic cell proliferation and acute myeloid leukemia with minimal differentiation (AML-M0)
- Failing methemoglobin blood gas analyses in a sodium nitrite intoxication