Stalmans Myrthe, Tominec Domen, Robberechts Ruben, Lauriks Wout, Ramaekers Monique, Debevec Tadej, Poffé Chiel
Exercise Physiology Research Group, Department of Movement Sciences, KU Leuven, Leuven, BELGIUM.
Faculty of Sport, University of Ljubljana, Ljubljana, SLOVENIA.
Med Sci Sports Exerc. 2025 Apr 1;57(4):807-819. doi: 10.1249/MSS.0000000000003604. Epub 2024 Nov 18.
Sleeping at altitude is highly common in athletes as an integral part of altitude training camps or sport competitions. However, concerns have been raised because of expected negative effects on sleep quality, thereby potentially hampering exercise recovery and next-day exercise performance. We recently showed that ketone ester (KE) ingestion beneficially impacted sleep after strenuous, late evening exercise in normoxia, and alleviated hypoxemia. Therefore, we hypothesized that KE ingestion may be an effective strategy to attenuate hypox(em)ia-induced sleep dysregulations.
Eleven healthy male participants completed three experimental sessions including normoxic training and subsequent sleep in normoxia or at a simulated altitude of 3000 m while receiving either KE or placebo postexercise and presleep. Sleep was evaluated using polysomnography, whereas next-day exercise performance was assessed through a 30-min all-out time trial (TT 30' ). Physiological measurements included oxygen status, heart rate variability, ventilatory parameters, blood acid-base balance, and capillary blood gases.
Hypoxia caused a ~3% drop in sleep efficiency, established through a doubled wakefulness after sleep onset and a ~22% reduction in slow wave sleep. KE ingestion alleviated the gradual drop in SpO 2 throughout the first part of the night, but did not alter hypoxia-induced sleep dysregulations. Neither KE nor nocturnal hypoxia affected TT 30' performance, but nocturnal hypoxia hampered heart rate recovery after TT 30' .
We observed that sleeping at a 3000 m altitude impairs sleep efficiency. Although this hypoxia-induced sleep disruption was too subtle to limit exercise performance, we for the first time indicate that sleeping at altitude might impair next-day exercise recovery. KE alleviated nocturnal hypoxemia only when SpO 2 values dropped below ~85%, but this did not translate into improved sleep or next-day exercise performance.
在高海拔地区睡眠在运动员中非常普遍,是高原训练营或体育比赛的一个组成部分。然而,由于预计会对睡眠质量产生负面影响,人们对此表示担忧,这可能会妨碍运动恢复和次日的运动表现。我们最近发现,摄入酮酯(KE)对常氧环境下深夜剧烈运动后的睡眠有有益影响,并减轻了低氧血症。因此,我们假设摄入KE可能是减轻低氧(血症)引起的睡眠失调的有效策略。
11名健康男性参与者完成了三个实验阶段,包括常氧训练以及随后在常氧环境或模拟海拔3000米的环境中睡眠,运动后和睡前分别接受KE或安慰剂。使用多导睡眠图评估睡眠,而次日的运动表现则通过30分钟全力计时赛(TT 30')进行评估。生理测量包括氧状态、心率变异性、通气参数、血液酸碱平衡和毛细血管血气。
低氧导致睡眠效率下降约3%,表现为入睡后清醒时间翻倍以及慢波睡眠减少约22%。摄入KE减轻了夜间第一阶段SpO₂的逐渐下降,但并未改变低氧引起的睡眠失调。KE和夜间低氧均未影响TT 30'的表现,但夜间低氧妨碍了TT 30'后心率的恢复。
我们观察到在海拔3000米的高度睡眠会损害睡眠效率。尽管这种由低氧引起的睡眠干扰过于轻微,不足以限制运动表现,但我们首次表明在高海拔地区睡眠可能会损害次日的运动恢复。只有当SpO₂值降至约85%以下时,KE才能减轻夜间低氧血症,但这并未转化为改善睡眠或次日的运动表现。