The ELSA trial: single versus combinatory effects of non-prohibited beta-2 agonists on skeletal muscle metabolism, cardio-pulmonary function and endurance performance-study protocol for a randomized 4-way balanced cross-over trial.

Anti-doping Asthma Asthma sprays Beta-2 agonists Cardiopulmonary function Endurance performance Ergogenic effects Exercise Randomized controlled trial Skeletal muscle/blood biomarkers WADA

Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
11 Dec 2021
Historique:
received: 06 07 2021
accepted: 22 11 2021
entrez: 13 12 2021
pubmed: 14 12 2021
medline: 15 12 2021
Statut: epublish

Résumé

Asthma and/or airway hyper-responsiveness (AHR) are common in elite endurance athletes with a high prevalence rate of beta-2 adrenoreceptor (beta-2) agonists use. Nevertheless, there are data on dose-dependent ergogenic effects of beta-2 agonists suggesting increased muscle strength, endurance and neuromuscular performance. Therefore, most beta-2 agonists belong to the World Anti Doping Agency (WADA) list of prohibited substances and it is tempting to speculate that illegitimate use of beta-2 agonists might be a common practice to boost performance in competitive sports. It is currently unknown whether or not inhaled beta-2 agonists enhance performance by stimulatory effects in skeletal and cardiac muscle. The ELSA trial is a double-blinded, placebo-controlled, randomized, balanced, four-way cross-over study. Study participants (n=24, 12 ♀, 12 ♂) complete four study arms (i.e. periods with treatment A, placebo; B, salbutamol; C, formoterol; D, formoterol + salbutamol) in random order after an initial preliminary testing session. Participants inhale the study medication 20 min before the 10-min time trial (TT; exercise performance test), where participants cycle 10 min at the highest possible workload. Cardiac output is measured continuously. A skeletal muscle biopsy is collected 3 h after the TT. Study endpoints include measures of skeletal muscle expression of nuclear receptors, hormones and cytokine levels, urinary and plasma concentrations of salbutamol and formoterol, circulating cardiac markers, cardiopulmonary function and exercise performance (average power and peak power during the TT). Blood and urine are collected and respiratory testing is performed 24 h post TT. This clinical trial evaluates the potential performance-enhancing effects of non-prohibited, not medically indicated inhaled short- and long-acting beta-2 agonists on skeletal muscle gene expression, endocrine regulation, cardiac biomarkers, cardiopulmonary function and acute endurance exercise performance. These data will be used by WADA to adapt the annually published list of prohibited substances (WADA 2021) and will be published in scientific journals. The trial is registered at the European Clinical Trials Database (Eudra CT) with the number: 2015-005598-19 as well as at the German register for clinical studies (DRKS number 00010574 ).

Sections du résumé

BACKGROUND BACKGROUND
Asthma and/or airway hyper-responsiveness (AHR) are common in elite endurance athletes with a high prevalence rate of beta-2 adrenoreceptor (beta-2) agonists use. Nevertheless, there are data on dose-dependent ergogenic effects of beta-2 agonists suggesting increased muscle strength, endurance and neuromuscular performance. Therefore, most beta-2 agonists belong to the World Anti Doping Agency (WADA) list of prohibited substances and it is tempting to speculate that illegitimate use of beta-2 agonists might be a common practice to boost performance in competitive sports. It is currently unknown whether or not inhaled beta-2 agonists enhance performance by stimulatory effects in skeletal and cardiac muscle.
METHODS METHODS
The ELSA trial is a double-blinded, placebo-controlled, randomized, balanced, four-way cross-over study. Study participants (n=24, 12 ♀, 12 ♂) complete four study arms (i.e. periods with treatment A, placebo; B, salbutamol; C, formoterol; D, formoterol + salbutamol) in random order after an initial preliminary testing session. Participants inhale the study medication 20 min before the 10-min time trial (TT; exercise performance test), where participants cycle 10 min at the highest possible workload. Cardiac output is measured continuously. A skeletal muscle biopsy is collected 3 h after the TT. Study endpoints include measures of skeletal muscle expression of nuclear receptors, hormones and cytokine levels, urinary and plasma concentrations of salbutamol and formoterol, circulating cardiac markers, cardiopulmonary function and exercise performance (average power and peak power during the TT). Blood and urine are collected and respiratory testing is performed 24 h post TT. This clinical trial evaluates the potential performance-enhancing effects of non-prohibited, not medically indicated inhaled short- and long-acting beta-2 agonists on skeletal muscle gene expression, endocrine regulation, cardiac biomarkers, cardiopulmonary function and acute endurance exercise performance. These data will be used by WADA to adapt the annually published list of prohibited substances (WADA 2021) and will be published in scientific journals.
TRIAL REGISTRATION BACKGROUND
The trial is registered at the European Clinical Trials Database (Eudra CT) with the number: 2015-005598-19 as well as at the German register for clinical studies (DRKS number 00010574 ).

Identifiants

pubmed: 34895300
doi: 10.1186/s13063-021-05862-w
pii: 10.1186/s13063-021-05862-w
pmc: PMC8665595
doi:

Substances chimiques

Albuterol QF8SVZ843E

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

903

Subventions

Organisme : world anti-doping agency - research grant
ID : 15C13MZ

Informations de copyright

© 2021. The Author(s).

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Auteurs

Martina Zügel (M)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Daniel A Bizjak (DA)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Dorle Nussbaumer (D)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Kay Winkert (K)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Kensuke Takabayashi (K)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.
Hirakata Kohsai Hospital, Hirakata, Osaka, Japan.

Johannes Kirsten (J)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Mickel Washington (M)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Gunnar Treff (G)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Jens Dreyhaupt (J)

Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.

Luise Steeb (L)

Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.

Patrick Diel (P)

Institute for Cardiovascular Research and Sports Medicine, Department of Molecular and Cellular Sports Medicine, German Sports University Cologne, Cologne, Germany.

Maria Kristina Parr (MK)

Institute of Pharmacy, Pharmaceutical and Medicinal Chemistry, Freie Universität Berlin, Berlin, Germany.

Jürgen M Steinacker (JM)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany.

Hasema Persch (H)

Division of Sports and Rehabilitation Medicine, Department of Internal Medicine II, University Hospital Ulm, Ulm, Germany. hasema.persch@uniklinik-ulm.de.

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Classifications MeSH