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
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
903Subventions
Organisme : world anti-doping agency - research grant
ID : 15C13MZ
Informations de copyright
© 2021. The Author(s).
Références
Br J Sports Med. 2006 Jul;40 Suppl 1:i43-7
pubmed: 16799103
Clin J Sport Med. 2011 Jan;21(1):46-50
pubmed: 21200170
Eur J Appl Physiol. 2013 Feb;113(2):411-8
pubmed: 22767151
Sports Med. 2021 Jul;51(7):1353-1376
pubmed: 33811295
J Asthma. 2012 Sep;49(7):744-9
pubmed: 22873287
Clin Sci (Lond). 1992 Nov;83(5):615-21
pubmed: 1335400
Eur J Appl Physiol Occup Physiol. 1987;56(6):679-85
pubmed: 3678222
J Appl Physiol (1985). 2017 Apr 1;122(4):997-1002
pubmed: 28153947
Int J Sports Med. 2004 Oct;25(7):533-8
pubmed: 15459835
Med Sci Sports Exerc. 2013 Oct;45(10):1925-32
pubmed: 23559124
Int J Pharm. 2009 May 8;372(1-2):91-6
pubmed: 19429271
Med Sci Sports Exerc. 2010 Feb;42(2):244-9
pubmed: 19927035
Eur J Clin Pharmacol. 1999 Apr;55(2):131-8
pubmed: 10335908
Br J Pharmacol. 2006 Mar;147(6):587-95
pubmed: 16432501
Eur Respir J. 1997 Aug;10(8):1820-3
pubmed: 9272925
Allergy Asthma Clin Immunol. 2010 Nov 30;6(1):31
pubmed: 21118543
Drug Test Anal. 2009 Nov;1(11-12):554-67
pubmed: 20355172
J Int Med Res. 2016 Aug;44(4):832-43
pubmed: 27142436
Arzneimittelforschung. 1992 Feb;42(2):163-72
pubmed: 1610429
BMJ. 2013 Jan 08;346:e7586
pubmed: 23303884
Drug Test Anal. 2012 Jun;4(6):449-54
pubmed: 22447497
Respiration. 2000;67(5):510-3
pubmed: 11070454
Scand J Med Sci Sports. 2014 Oct;24(5):814-22
pubmed: 23834392
Pharmacotherapy. 2011 Aug;31(8):748-56
pubmed: 21923601
Scand J Med Sci Sports. 2015 Feb;25(1):e20-7
pubmed: 24646113
Bioanalysis. 2009 May;1(2):437-50
pubmed: 21083176
Sports Med. 2002;32(9):583-600
pubmed: 12096931
Scand J Med Sci Sports. 2012 Apr;22(2):232-9
pubmed: 21083771
Br J Sports Med. 2012 May;46(6):413-6
pubmed: 22228581