Multiple sclerosis-related fatigue: the role of impaired corticospinal responses and heightened exercise fatigability

• Published in: Journal of neurophysiology Vol. 124; no. 4; pp. 1131 - 1143
• Main Authors: Coates, Kyla D., Aboodarda, Saied Jalal, Krüger, Renata L., Martin, Tristan, Metz, Luanne M., Jarvis, Scott E., Millet, Guillaume Y.
• Format: Journal Article
• Language: English
• Published: American Physiological Society 01.10.2020
• Subjects: Cancer; Life Sciences; Neurons and Cognition; Other; Multiple Sclerosis; Transcranial Magnetic Stimulation; Fatigue; Motor Evoked Potentials; Neuromuscular Fatigue
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00165.2020

The etiology of fatigability from whole body exercise was examined for the first time to accurately elucidate the relationship between fatigue and fatigability in multiple sclerosis (MS). Compromised corticospinal responsiveness predicted fatigue severity, providing a novel, objective indicator of fatigue in MS. Although the impaired corticomotor transmission did not aggravate muscle activation in this group of people with multiple sclerosis (PwMS) of lower disability, heightened muscle fatigability was seen to contribute to perceptions of fatigue in PwMS. It is unclear whether motor fatigability and perceived fatigue share a common pathophysiology in people with multiple sclerosis (PwMS). This cross-sectional investigation explored the relationship between the mechanisms of motor fatigability from cycling and fatigue severity in PwMS. Thirteen highly fatigued (HF) and thirteen nonfatigued (LF) PwMS and thirteen healthy controls (CON) completed a step test until volitional exhaustion on an innovative cycle ergometer. Neuromuscular evaluations involving femoral nerve electrical stimulation and transcranial magnetic stimulation were performed every 3 min throughout cycling. One-way ANOVA at baseline and exhaustion uncovered evidence of consistently smaller motor evoked potential (MEP) amplitudes ( P = 0.011) and prolonged MEP latencies ( P = 0.041) in HF as well as a greater decline in maximal voluntary contraction force (HF: 63 ± 13%; LF: 75 ± 13%; CON: 73 ± 11% of pre; P = 0.037) and potentiated twitch force (HF: 35 ± 13%; LF: 50 ± 16%; CON: 47 ± 17% of pre; P = 0.049) in HF at volitional exhaustion. Hierarchical regression determined that fatigue severity on the Fatigue Severity Scale was predicted by prolonged MEP latencies (change in r 2  = 0.389), elevated peripheral muscle fatigability (change in r 2  = 0.183), and depressive symptoms (change in r 2  = 0.213). These findings indicate that MS-related fatigue is distinguished by disrupted corticospinal responsiveness, which could suggest progressive pathology, but fatigability from whole body exercise and depressive symptoms also influence perceptions of fatigue in PwMS. NEW & NOTEWORTHY The etiology of fatigability from whole body exercise was examined for the first time to accurately elucidate the relationship between fatigue and fatigability in multiple sclerosis (MS). Compromised corticospinal responsiveness predicted fatigue severity, providing a novel, objective indicator of fatigue in MS. Although the impaired corticomotor transmission did not aggravate muscle activation in this group of people with multiple sclerosis (PwMS) of lower disability, heightened muscle fatigability was seen to contribute to perceptions of fatigue in PwMS.