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ELSA 试验:非禁用β2 激动剂对骨骼肌代谢、心肺功能和耐力表现的单一与联合作用——一项随机 4 向平衡交叉试验的研究方案。

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.

机构信息

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

Hirakata Kohsai Hospital, Hirakata, Osaka, Japan.

出版信息

Trials. 2021 Dec 11;22(1):903. doi: 10.1186/s13063-021-05862-w.

Abstract

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

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

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 ).

摘要

背景

哮喘和/或气道高反应性(AHR)在精英耐力运动员中很常见,β-2 肾上腺素能受体(β-2)激动剂的使用率也很高。然而,有数据表明β-2 激动剂具有剂量依赖性的促效作用,可增加肌肉力量、耐力和神经肌肉表现。因此,大多数β-2 激动剂都被世界反兴奋剂机构(WADA)列入违禁物质清单,人们不禁猜测,非法使用β-2 激动剂可能是提高竞技体育成绩的常见做法。目前尚不清楚吸入β-2 激动剂是否通过对骨骼肌和心肌的刺激作用来提高运动表现。

方法

ELSA 试验是一项双盲、安慰剂对照、随机、平衡、四交叉研究。研究参与者(n=24,12 名女性,12 名男性)在初始预测试阶段后,以随机顺序完成四项研究臂(即 A 臂治疗药物 A、安慰剂;B 臂沙丁胺醇;C 臂福莫特罗;D 臂福莫特罗+沙丁胺醇)。参与者在 10 分钟时间试验(TT;运动表现测试)前 20 分钟吸入研究药物,在此期间,参与者以最高可能的工作量骑自行车 10 分钟。心输出量连续测量。TT 后 3 小时采集骨骼肌活检。研究终点包括骨骼肌核受体、激素和细胞因子水平的表达、沙丁胺醇和福莫特罗的尿和血浆浓度、循环心脏标志物、心肺功能和运动表现(TT 期间的平均功率和峰值功率)。TT 后 24 小时采集血液和尿液,并进行呼吸测试。这项临床试验评估了非禁用、非医学指征的吸入短效和长效β-2 激动剂对骨骼肌基因表达、内分泌调节、心脏标志物、心肺功能和急性耐力运动表现的潜在增强作用。这些数据将由 WADA 用于调整每年公布的违禁物质清单(WADA 2021),并在科学期刊上发表。

试验注册

该试验在欧洲临床试验数据库(Eudra CT)注册,编号为:2015-005598-19,并在德国临床研究注册处(DRKS 编号 00010574)注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f024/8665595/6db18e20ac34/13063_2021_5862_Fig1_HTML.jpg

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