Effects of Inhaled β <sub>2</sub> ‐ <scp>AR</scp> Agonists in Athletes According to the <scp>WADA</scp> 2025 List: New Insights From a Systematic Review and Meta‐Analysis

This systematic review and meta-analysis (CRD420251006746) investigated the impact of inhaled β<sub>2</sub>-adrenoceptor (AR) agonists (IBA) with exemption according to the World Anti-Doping Agency (WADA) 2025 list on athletic performance, respiratory, and cardiovascular outcomes. A key subgroup analysis focused on IBA administered within WADA 2025 permitted dose intervals. Findings indicate that IBA significantly improved sprint time by 0.30 s (95% CI 0.52-0.07) overall, and by 0.27 s (95% CI 0.50-0.05) in healthy subjects, with long-acting β<sub>2</sub>-AR agonists yielding a 0.49 s (95% CI 0.81-0.17) improvement. These sprint time enhancements persisted even at WADA-permitted doses. Blood lactate levels significantly increased by 0.67 mmol/L (95% CI 0.19-1.14) overall and by 0.65 mmol/L (95% CI 0.17-1.14) in healthy subjects, though this effect was not significant at WADA-permitted doses. IBA significantly improved forced expiratory volume in 1 s by 0.19 L (95% CI 0.14-0.23) and forced expiratory flow between 25% and 75% by 0.40 L/s (95% CI 0.24-0.56), with lung function improvements confirmed at WADA-permitted doses. Heart rate significantly increased by 1.40 bpm (95% CI 0.32-2.48). IBA did not influence aerobic performance. When administered within WADA 2025 permitted doses, IBA can provide small but relevant gains in anaerobic performance in healthy individuals, while simultaneously offering therapeutic bronchodilation for athletes with asthma or exercise-induced bronchoconstriction. Dose restrictions are critical to minimize the risk of performance enhancement that exceeds therapeutic intent and to mitigate adverse effects. Further research is pivotal to ensure that anti-doping policies align with health standards and ethical considerations for all athletes.

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Journal
Scandinavian Journal of Medicine and Science in Sports
Published
2025-12-31
DOI
https://doi.org/10.1111/sms.70197
Primary Topic
Pharmacological Effects and Assays
Type
article
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article

Effects of Inhaled β 2 ‐ AR Agonists in Athletes According to the WADA 2025 List: New Insights From a Systematic Review and Meta‐Analysis

Saverio Muscoli, Paola Paola Rogliani, Gian Marco Manzetti, Josuel Ora et al.
Scandinavian Journal of Medicine and Science in Sports
Pharmacological Effects and Assays
article

Effects of Inhaled β 2 ‐ AR Agonists in Athletes According to the WADA 2025 List: New Insights From a Systematic Review and Meta‐Analysis

Saverio Muscoli, Paola Paola Rogliani, Gian Marco Manzetti, Josuel Ora, LUIGINO CALZETTA, Shima Gholamalishahi, Elena Pistocchini, Miriana Cammarata
article en

Abstract

This systematic review and meta-analysis (CRD420251006746) investigated the impact of inhaled β<sub>2</sub>-adrenoceptor (AR) agonists (IBA) with exemption according to the World Anti-Doping Agency (WADA) 2025 list on athletic performance, respiratory, and cardiovascular outcomes. A key subgroup analysis focused on IBA administered within WADA 2025 permitted dose intervals. Findings indicate that IBA significantly improved sprint time by 0.30 s (95% CI 0.52-0.07) overall, and by 0.27 s (95% CI 0.50-0.05) in healthy subjects, with long-acting β<sub>2</sub>-AR agonists yielding a 0.49 s (95% CI 0.81-0.17) improvement. These sprint time enhancements persisted even at WADA-permitted doses. Blood lactate levels significantly increased by 0.67 mmol/L (95% CI 0.19-1.14) overall and by 0.65 mmol/L (95% CI 0.17-1.14) in healthy subjects, though this effect was not significant at WADA-permitted doses. IBA significantly improved forced expiratory volume in 1 s by 0.19 L (95% CI 0.14-0.23) and forced expiratory flow between 25% and 75% by 0.40 L/s (95% CI 0.24-0.56), with lung function improvements confirmed at WADA-permitted doses. Heart rate significantly increased by 1.40 bpm (95% CI 0.32-2.48). IBA did not influence aerobic performance. When administered within WADA 2025 permitted doses, IBA can provide small but relevant gains in anaerobic performance in healthy individuals, while simultaneously offering therapeutic bronchodilation for athletes with asthma or exercise-induced bronchoconstriction. Dose restrictions are critical to minimize the risk of performance enhancement that exceeds therapeutic intent and to mitigate adverse effects. Further research is pivotal to ensure that anti-doping policies align with health standards and ethical considerations for all athletes.

Scandinavian Journal of Medicine and Science in SportsVol. 36(1)
University of Rome Tor Vergata (IT), University of Parma (IT), Policlinico Tor Vergata (IT)
Good health and well-being
Openalex Percentile: Top 35%
Pharmacological Effects and Assays
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