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This pilot study will evaluate for the presence of neuromuscular junction (NMJ) defect in women with motor fatigue in multiple sclerosis by Single Fiber Electromyography (SFEMG) using the concentric needle electrode.
Full description
The investigators will recruit 20 women with multiple sclerosis (MS) and fatigue and 10 normal controls with no identified causes of fatigue (no history of thyroid disease, anemia, liver disease, kidney disease, myasthenia gravis, and no major fatigue inducing medications). We will include MS patients with fatigue severity scale of ≥5. Patients with sleep disorders or significant depression will be excluded based on history, Epworth Sleepiness scale, and Beck's Inventory of Depression Scale. The study will include two clinic visits and a one-study visit. After informed consent is obtained (English and Spanish forms will be available), the following will be done during the study visit 1:
Neurological examination: Using handgrip dynamometer of the dominant hand.
Expanded Disability Status Scale (EDSS
Fatigue severity scale (FSS) and modified fatigue impact scale (MFIS)
Epworth Sleepiness scale for screening for sleep disorders.
Beck's Inventory of Depression Scale for screening for depression. Clinic visit 2: The clinic visit 2 will be conducted 5-30 days after the clinic visit 1
Neurological examination: Using handgrip dynamometer of the dominant hand.
Fatigue severity scale (FSS) and modified fatigue impact scale (MFIS)
Study Visit 3:
Electromyography (EMG) and SFEMG (Single Fiber Electromyography) of the extensor digitorum communis muscle (forearm muscle) will be performed on all women with fatigue and healthy controls at the TTUHSC electrophysiology lab to evaluate for NMJ abnormalities. The mean consecutive difference (MCD) of 20 pairs of single muscle fiber potentials will be collected using SFEMG from each of the 20 women with multiple sclerosis and fatigue and will be compared to MCD of 200 pair potentials from our recruited 10 normal control subjects and also to the previously published normative data.
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Inclusion criteria
Inclusion Criteria for MS Group (20 women)
Inclusion Criteria for Control Group (10 women)
Exclusion criteria
Patients with MS exacerbation or corticosteroid treatment within one month before the study.
Patients with history or current diagnosis of:
Taking major fatigue inducing medications. (e.g. Narcotics, and Sedatives)
Taking anticoagulation therapy. (e.g. warfarin and heparin)
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Data sourced from clinicaltrials.gov
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