Heuberger Jules A A C, Rotmans Joris I, Gal Pim, Stuurman Frederik E, van 't Westende Juliëtte, Post Titiaan E, Daniels Johannes M A, Moerland Matthijs, van Veldhoven Peter L J, de Kam Marieke L, Ram Herman, de Hon Olivier, Posthuma Jelle J, Burggraaf Jacobus, Cohen Adam F
Centre for Human Drug Research, Leiden, Netherlands.
Department of Internal Medicine, Leiden University Medical Centre, Leiden, Netherlands.
Lancet Haematol. 2017 Aug;4(8):e374-e386. doi: 10.1016/S2352-3026(17)30105-9. Epub 2017 Jun 29.
Substances that potentially enhance performance (eg, recombinant human erythropoietin [rHuEPO]) are considered doping and are therefore forbidden in sports; however, the scientific evidence behind doping is frequently weak. We aimed to determine the effects of rHuEPO treatment in well trained cyclists on maximal, submaximal, and race performance and on safety, and to present a model clinical study for doping research on other substances.
We did this double-blind, randomised, placebo-controlled trial at the Centre for Human Drug Research in Leiden (Netherlands). We enrolled healthy, well trained but non-professional male cyclists aged 18-50 years and randomly allocated (1:1) them to receive abdominal subcutaneous injections of rHuEPO (epoetin β; mean dose 6000 IU per week) or placebo (0·9% NaCl) for 8 weeks. Randomisation was stratified by age groups (18-34 years and 35-50 years), with a code generated by a statistician who was not masked to the study. The primary outcome was exercise performance, measured as maximal power output (Pmax), maximal oxygen consumption VO max, and gross efficiency in maximal exercise tests with 25 W increments per 5 min, as lactate threshold and ventilatory threshold 1 (VT1) and 2 (VT2) at submaximal levels during the maximal exercise test, and as mean power, VO, and heart rate in the submaximal exercise tests at the highest mean power output for 45 min in a laboratory setting and in a race to the Mont Ventoux (France) summit, using intention-to-treat analyses. The trial is registered with the Dutch Trial Registry (Nederlands Trial Register), number NTR5643.
Between March 7, 2016, and April 13, 2016, we randomly assigned 48 participants to the rHuEPO group (n=24) or the placebo group (n=24). Mean haemoglobin concentration (9·6 mmol/L vs 9·0 mmol/L [estimated difference 0·6, 95% CI 0·4 to 0·8]) and maximal power output (351·55 W vs 341·23 W [10·32, 3·47 to 17·17]), and VO max (60·121 mL/min per kg vs 57·415 mL/min per kg [2·707, 0·911 to 4·503]) in a maximal exercise test were higher in the rHuEPO group compared with the placebo group. Submaximal exercise test parameters mean power output (283·18 W vs 277·28 W [5·90, -0·87 to 12·67]) and VO (50·288 mL/min per kg vs 49·642 mL/min per kg [0·646, -1·307 to 2·600]) at day 46, and Mont Ventoux race times (1 h 40 min 32 s vs 1 h 40 min 15 s [0·3%, -8·3 to 9·6]) did not differ between groups. All adverse events were grade 1-2 and were similar between both groups. No events of grade 3 or worse were observed.
Although rHuEPO treatment improved a laboratory test of maximal exercise, the more clinically relevant submaximal exercise test performance and road race performance were not affected. This study shows that clinical studies with doping substances can be done adequately and safely and are relevant in determining effects of alleged performance-enhancing drugs.
Centre for Human Drug Research, Leiden.
具有潜在提高运动成绩作用的物质(如重组人促红细胞生成素[rHuEPO])被视为兴奋剂,因此在体育赛事中被禁用;然而,支持使用兴奋剂的科学证据往往不足。我们旨在确定rHuEPO治疗对训练有素的自行车运动员最大、次最大运动能力和比赛成绩以及安全性的影响,并为其他物质的兴奋剂研究提供一个典型的临床研究范例。
我们在荷兰莱顿的人类药物研究中心进行了这项双盲、随机、安慰剂对照试验。我们招募了年龄在18 - 50岁、健康、训练有素但非专业的男性自行车运动员,并将他们随机(1:1)分配接受腹部皮下注射rHuEPO(促红细胞生成素β;平均剂量为每周6000 IU)或安慰剂(0.9%氯化钠),为期8周。随机分组按年龄组(18 - 34岁和35 - 50岁)分层,由一位不了解研究情况的统计学家生成编码。主要结局是运动表现,通过最大运动测试中的最大功率输出(Pmax)、最大耗氧量VO₂max以及每5分钟增加25 W的最大运动测试中的总效率来衡量,还包括最大运动测试中次最大运动水平时的乳酸阈值和通气阈值1(VT1)和2(VT2),以及在实验室环境中以最高平均功率输出进行45分钟的次最大运动测试和法国旺图山比赛中的平均功率、VO₂和心率,采用意向性分析。该试验已在荷兰试验注册中心(荷兰试验注册)注册,注册号为NTR5643。
在2016年3月7日至2016年4月13日期间,我们将48名参与者随机分配至rHuEPO组(n = 24)或安慰剂组(n = 24)。与安慰剂组相比,rHuEPO组在最大运动测试中的平均血红蛋白浓度(9.6 mmol/L对9.0 mmol/L[估计差值0.6,95%CI 0.4至0.8])、最大功率输出(351.55 W对341.23 W[10.32,3.47至17.17])和VO₂max(60.121 mL/min per kg对57.415 mL/min per kg[2.707,0.911至4.503])更高。两组在第46天的次最大运动测试参数平均功率输出(283.18 W对277.28 W[5.90, -0.87至12.67])和VO₂(50.288 mL/min per kg对49.642 mL/min per kg[0.646, -1.307至2.600])以及旺图山比赛时间(1小时40分32秒对1小时40分15秒[0.3%, -8.3至9.6])方面无差异。所有不良事件均为1 - 2级,两组相似。未观察到3级或更严重的事件。
尽管rHuEPO治疗改善了最大运动的实验室测试结果,但与临床相关性更强的次最大运动测试表现和公路赛成绩并未受到影响。这项研究表明,关于兴奋剂物质的临床研究可以充分且安全地进行,并且对于确定所谓的提高成绩药物的效果具有重要意义。
莱顿人类药物研究中心。