Surface EMG of proximal leg muscles in neuromuscular patients and in healthy controls. Relations to force and fatigue.

In an effort to find parameters to evaluate patients with neuromuscular disorders, surface electromyography (SEMG) of proximal leg muscles was performed in 33 patients with myotonic dystrophy (MyD), 29 patients with Charcot-Marie-Tooth (CMT) disease and 20 healthy controls. The root mean square (RMS) of the SEMG amplitude (microV) was calculated at different torque levels. Endurance (seconds) and median frequency (Fmed) of the SEMG power spectrum, used as parameters of fatigue, were determined at 80% of MVC. Maximum voluntary contraction (MVC) was found to be decreased in patients; the ratio between RMS values of antagonists and agonists was increased and torque-EMG ratios (Nm/microV) were decreased. These differences with respect to controls were more pronounced in MyD than in CMT. The initial Fmed value was lowest in CMT. The greatest decrease in Fmed was found in MyD. SEMG data in relation to force have not been determined before in groups of MyD or CMT patients. In both disorders, parameters differed from controls, which means that adding SEMG to strength measurements could be useful in studying the progress of the disorder and the effects of interventions.

[1]  R. Stein,et al.  Contractile and electrical properties of human motor units in neuropathies and motor neurone disease , 1974, Journal of neurology, neurosurgery, and psychiatry.

[2]  A. Emery Population frequencies of inherited neuromuscular diseases—A world survey , 1991, Neuromuscular Disorders.

[3]  Y. Jammes,et al.  EMG power spectrum of respiratory and skeletal muscles during static contraction in healthy man , 1993, Muscle & nerve.

[4]  In vivo quantification of muscle contractility in humans: healthy subjects and patients with myotonic muscular dystrophy. , 1992, Archives of physical medicine and rehabilitation.

[5]  M. McCrory,et al.  Moderate resistance exercise program: its effect in slowly progressive neuromuscular disease. , 1993, Archives of physical medicine and rehabilitation.

[6]  J Drukker,et al.  Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: a randomized clinical trial. , 1995, Archives of physical medicine and rehabilitation.

[7]  Anders Fuglsang-Frederiksen,et al.  EMG power spectrum, turns-amplitude analysis and motor unit potential duration in neuromuscular disorders , 1990, Journal of the Neurological Sciences.

[8]  T. Mulder,et al.  The effects of fatigue and task repetition on the surface electromyographic signal. , 1984, Psychophysiology.

[9]  H. Milner-Brown,et al.  Quantifying human muscle strength, endurance and fatigue. , 1986, Archives of physical medicine and rehabilitation.

[10]  J Drukker,et al.  Quadriceps strength and timed motor performances in myotonic dystrophy, Charcot–Marie–Tooth disease, and healthy subjects , 1998, Clinical rehabilitation.

[11]  H J Hermens,et al.  The clinical use of surface EMG. , 1984, Electromyography and clinical neurophysiology.

[12]  T. Housh,et al.  LINEARITY AND RELIABILITY OF THE IEMG V TORQUE RELATIONSHIP FOR THE FOREARM FLEXORS AND LEG EXTENSORS , 1992, American journal of physical medicine & rehabilitation.

[13]  D. Stegeman,et al.  Fatigue in type I fiber predominance: A muscle force and surface EMG study on the relative role of type I and type II muscle fibers , 1991, Muscle & nerve.

[14]  Miller Rg,et al.  Muscle strengthening through electric stimulation combined with low-resistance weights in patients with neuromuscular disorders. , 1988 .

[15]  A. McComas,et al.  The effects of strength training in patients with selected neuromuscular disorders. , 1988, Medicine and science in sports and exercise.

[16]  I Yaar,et al.  Muscle fiber conduction velocity and mean power spectrum frequency in neuromuscular disorders and in fatigue , 1992, Muscle & nerve.

[17]  A. McComas,et al.  Contractile properties of muscles in myotonic dystrophy. , 1983, Journal of neurology, neurosurgery, and psychiatry.

[18]  J. Lenman QUANTITATIVE ELECTROMYOGRAPHIC CHANGES ASSOCIATED WITH MUSCULAR WEAKNESS , 1959, Journal of neurology, neurosurgery, and psychiatry.

[19]  M. Zwarts,et al.  Transient paresis in myotonic syndromes. A surface EMG study. , 1989, Brain : a journal of neurology.

[20]  H. Milner-Brown,et al.  Muscle strengthening through high-resistance weight training in patients with neuromuscular disorders. , 1988, Archives of physical medicine and rehabilitation.

[21]  B. Bigland-ritchie,et al.  Linear and non-linear surface EMG/force relationships in human muscles. An anatomical/functional argument for the existence of both. , 1983, American journal of physical medicine.

[22]  M. McCrory,et al.  The effect of a high resistance exercise program in slowly progressive neuromuscular disease. , 1994, Archives of physical medicine and rehabilitation.

[23]  W Herzog,et al.  Assessment of muscular fatigue using vibromyography , 1994, Muscle & nerve.

[24]  T Moritani,et al.  Surface EMG power spectral analysis of neuromuscular disorders during isometric and isotonic contractions. , 1982, American journal of physical medicine.

[25]  T. Moritani,et al.  Neural factors versus hypertrophy in the time course of muscle strength gain. , 1979, American journal of physical medicine.