Investigation of hand muscle atrophy in stroke survivors.

BACKGROUND Weakness is often profound in the contralesional hand after stroke. Relative contributions of various neural and mechanical mechanisms to this impairment, however, have not been quantified. In this study, the extent of one potential contributor, muscle atrophy, was noninvasively assessed in index finger musculature using ultrasonographic techniques. METHODS Twenty-five stroke survivors (45-65 years old) with severe hand impairment resulting from a stroke occurring 2-4 years prior participated, along with 10 age-matched control subjects. Muscle cross sectional area and thickness were geometrically measured from ultrasound images on both limbs of participants. FINDINGS Muscle size on the paretic limb of stroke survivors was smaller for all 7 hand muscles investigated. An average difference of 15% (SD 4) was seen for muscle cross sectional area and 11% (SD 2) for muscle thickness, while the difference between the dominant and non-dominant limbs for control subjects (6% (SD 2) and 1% (SD 4) for the muscle cross sectional area and muscle thickness, respectively) was not significant. INTERPRETATION Although muscle atrophy was detected in the paretic limb following stroke, it is not explanatory of the marked impairment in strength seen in this stroke population. However, other alterations in muscle morphology, such as fatty infiltrations and changes in fiber structure, may contribute to the emergent muscle weakness post-stroke.

[1]  U. Slager,et al.  Fiber composition and morphometry of the quadriceps femoris muscle in athletes and non-athletic individuals after knee injury. , 1985, Journal of Sports Medicine and Physical Fitness.

[2]  R. Lieber,et al.  Architecture of selected wrist flexor and extensor muscles. , 1990, The Journal of hand surgery.

[3]  Dina Brooks,et al.  Voluntary activation failure contributes more to plantar flexor weakness than antagonist coactivation and muscle atrophy in chronic stroke survivors. , 2010, Journal of applied physiology.

[4]  J. Fleg,et al.  Muscle quality. I. Age-associated differences between arm and leg muscle groups. , 1999, Journal of applied physiology.

[5]  Takashi Abe,et al.  Prediction and validation of total and regional skeletal muscle mass by ultrasound in Japanese adults , 2005, European Journal of Applied Physiology.

[6]  Kai-yu Tong,et al.  The mechanomyography of persons after stroke during isometric voluntary contractions. , 2007, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

[7]  M. Johnson,et al.  Data on the distribution of fibre types in thirty-six human muscles. An autopsy study. , 1973, Journal of the neurological sciences.

[8]  D G Kamper,et al.  Kinetic and kinematic workspaces of the index finger following stroke. , 2005, Brain : a journal of neurology.

[9]  R. Lieber,et al.  Architectural design of the human intrinsic hand muscles. , 1992, The Journal of hand surgery.

[10]  R. Macko,et al.  Skeletal muscle changes after hemiparetic stroke and potential beneficial effects of exercise intervention strategies. , 2008, Journal of rehabilitation research and development.

[11]  Constantinos N. Maganaris,et al.  Ultrasonographic assessment of human skeletal muscle size , 2003, European Journal of Applied Physiology.

[12]  P Girlanda,et al.  Muscle rearrangement in patients with hemiparesis after stroke: an electrophysiological and morphological study. , 1993, European neurology.

[13]  A. Macaluso,et al.  Muscle strength, power and adaptations to resistance training in older people , 2004, European Journal of Applied Physiology.

[14]  B. Clark,et al.  Evaluation of spastic muscle in stroke survivors using magnetic resonance imaging and resistance to passive motion. , 2006, Archives of physical medicine and rehabilitation.

[15]  K. J. Lutz,et al.  A cross-sectional study of muscle strength and mass in 45- to 78-yr-old men and women. , 1991, Journal of applied physiology.

[16]  F. Zajac Muscle and tendon: properties, models, scaling, and application to biomechanics and motor control. , 1989, Critical reviews in biomedical engineering.

[17]  D F Stegeman,et al.  Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders. , 2006, Journal of applied physiology.

[18]  E. G. Cruz,et al.  Weakness is the primary contributor to finger impairment in chronic stroke. , 2006, Archives of physical medicine and rehabilitation.

[19]  W. Evans,et al.  Sarcopenia and age-related changes in body composition and functional capacity. , 1993, The Journal of nutrition.

[20]  R. Lieber,et al.  Architecture of selected muscles of the arm and forearm: anatomy and implications for tendon transfer. , 1992, The Journal of hand surgery.

[21]  Richard L Lieber,et al.  Spasticity causes a fundamental rearrangement of muscle–joint interaction , 2002, Muscle & nerve.

[22]  B. Saltin,et al.  Muscle metabolism during exercise in hemiparetic patients. , 1977, Clinical science and molecular medicine.

[23]  C. D. De Luca,et al.  Effects of muscle fiber type and size on EMG median frequency and conduction velocity. , 1995, Journal of applied physiology.

[24]  Fan Gao,et al.  Altered contractile properties of the gastrocnemius muscle poststroke. , 2008, Journal of applied physiology.

[25]  C. Reimers,et al.  Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in 350 patients and review of the literature , 1996, Journal of the Neurological Sciences.

[26]  R. Parry Chedoke-McMaster Stroke Assessment — Development, Validation and Administration Manual , 1996 .

[27]  C. Reimers,et al.  Age-related muscle atrophy does not affect all muscles and can partly be compensated by physical activity: An ultrasound study 1 Presented in part at the 34th German Congress of Sports Medicine in Saarbrücken/Germany, October 19–22, 1995 [8]. 1 , 1998, Journal of the Neurological Sciences.