Article Text
Abstract
Introduction Athletes have attempted to glean the ergogenic benefits of recombinant human erythropoietin (rHuEPO) since it became available in the 1980s. However, there is limited consensus in the literature regarding its true performance-enhancing effects. In fact, some studies suggest there is no conclusive evidence; therefore, it is necessary to evaluate and quantify the strength of the evidence.
Objective To determine the effects of erythropoietin on enhancing athletic performance.
Design At least two independent reviewers conducted citation identification through abstract and full-text screening, and study selection, and extracted raw data on demographics, descriptions of interventions and all outcomes to predesigned abstraction forms. Outcomes were stratified by treatment periods and dosages. Study quality was assessed using the Cochrane Risk of Bias Tool and Cochrane Grading of Recommendations Assessment Development and Education (GRADE) scale. Where appropriate, quantitative analysis was performed.
Data sources EMBASE, MEDLINE and SPORTDiscus were searched from their inception to January 2020.
Eligibility criteria Trials that examined any enhancement in sport in healthy participants aged 18–65 using rHuEPO compared with placebo were included.
Results Overall, there is low-to-moderate quality evidence suggesting rHuEPO may be more beneficial than placebo in enhancing haematological parameters, pulmonary measures, maximal power output and time to exhaustion independent of dosage. However, these improvements are almost exclusively seen during maximal exercise intensities, which may be less relevant to athletic competition conditions.
Conclusion Due to heterogeneity among trials, more high-quality randomised controlled trials with larger sample sizes in conditions that mirror actual competition are needed to further elucidate these effects.
- EPO
- erythropoietin
- doping
- athletic performance
- systematic review
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Footnotes
Contributors KVT and DD contributed to design, data abstraction, study appraisal, data analysis, manuscript drafting and approval of the final manuscript. KJQC contributed to data abstraction, study appraisal, data analysis, manuscript drafting and approval of the final manuscript. LH contributed to study appraisal, data analysis, manuscript drafting and approval of the final manuscript. OG contributed to data abstraction, manuscript drafting and approval of the final manuscript.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval Research ethics approval was not obtained because this study did not directly involve human participants. There was no personal and/or medical information about an identifiable living individual in our study.
Provenance and peer review Not commissioned; externally peer reviewed.