Inter-University Laboratory of Human Movement Sciences (LIBM) EA7424, Team "Vascular Biology and Red Blood Cell", University Claude Bernard Lyon 1, Villeurbanne, France.
Laboratory of Excellence "GR-Ex", Paris, France.
Eur J Appl Physiol. 2021 Sep;121(9):2459-2470. doi: 10.1007/s00421-021-04716-2. Epub 2021 May 22.
Sickle cell disease (SCD) patients exhibit a limited exercise tolerance commonly attributed to anaemia, as well as hemorheological and cardio-respiratory abnormalities, but the functional status of skeletal muscle at exercise is unknown. Moreover, the effect of SCD genotype on exercise tolerance and skeletal muscle function has been poorly investigated. The aim of this study was to investigate skeletal muscle function and fatigue during a submaximal exercise in SCD patients.
Nineteen healthy individuals (AA), 28 patients with sickle cell anaemia (SS) and 18 with sickle cell-haemoglobin C disease (SC) performed repeated knee extensions exercise (FAT). Maximal isometric torque (Tmax) was measured before and after the FAT to quantify muscle fatigability. Electromyographic activity and oxygenation by near-infrared spectroscopy of the Vastus Lateralis were recorded.
FAT caused a reduction in Tmax in SS (- 17.0 ± 12.1%, p < 0.001) and SC (- 21.5 ± 14.5%, p < 0.05) but not in AA (+ 0.58 ± 29.9%). Root-mean-squared value of EMG signal (RMS) decreased only in SS after FAT, while the median power frequency (MPF) was unchanged in all groups. Oxygenation kinetics were determined in SS and AA and were not different.
These results show skeletal muscle dysfunction during exercise in SCD patients, and suggest different fatigue aetiology between SS and SC. The changes in EMG signal and oxygenation kinetics during exercise suggest that the greater skeletal muscle fatigue occurring in SCD patients would be rather due to intramuscular alterations modifications than decreased tissue oxygenation. Moreover, SS patients exhibit greater muscle fatigability than SC.
镰状细胞病(SCD)患者表现出运动耐量有限,通常归因于贫血以及血液流变学和心肺异常,但运动时骨骼肌的功能状态尚不清楚。此外,SCD 基因型对运动耐力和骨骼肌功能的影响尚未得到充分研究。本研究旨在研究 SCD 患者在亚最大运动期间的骨骼肌功能和疲劳。
19 名健康个体(AA)、28 名镰状细胞贫血(SS)患者和 18 名镰状细胞-血红蛋白 C 病(SC)患者进行了重复膝关节伸展运动(FAT)。在 FAT 前后测量最大等长扭矩(Tmax),以量化肌肉疲劳性。记录股外侧肌的肌电图活动和近红外光谱的氧合作用。
FAT 导致 SS(-17.0±12.1%,p<0.001)和 SC(-21.5±14.5%,p<0.05)的 Tmax 降低,但 AA 没有(+0.58±29.9%)。在 FAT 后,仅 SS 的肌电图信号均方根值(RMS)降低,而所有组的中值功率频率(MPF)均未改变。在 SS 和 AA 中确定了氧合动力学,它们没有差异。
这些结果表明 SCD 患者在运动时骨骼肌功能障碍,并表明 SS 和 SC 之间的疲劳病因不同。运动过程中肌电图信号和氧合动力学的变化表明,SCD 患者发生的更大骨骼肌疲劳主要是由于肌肉内变化修饰,而不是组织氧合降低所致。此外,SS 患者的肌肉疲劳性比 SC 更大。