Electrodiagnostic findings in amyotrophic lateral sclerosis: Variation with region of onset and utility of thoracic paraspinal muscle examination
Nirav Sanghani, Benjamin Claytor, Yuebing Li- Physiology (medical)
- Cellular and Molecular Neuroscience
- Neurology (clinical)
- Physiology
Abstract
Introduction/Aims
Limited data exist regarding variation of electrodiagnostic (EDX) findings in amyotrophic lateral sclerosis (ALS) patients with different onset regions and specificity of thoracic paraspinal muscle (TPSP) examination for confirming a diagnosis of ALS. We aimed to demonstrate the variation of EDX features and characterize the utility of TPSP muscle examination in the electrodiagnosis of ALS.
Methods
This is a retrospective study of a large cohort of ALS patients who had a comprehensive EDX evaluation.
Results
The study included 448 patients; all fulfilled the Gold Coast criteria for ALS. The average age at the time of EDX study was 64 years, and 41.1% were women. The onset region was identified as follows: bulbar (N = 149), cervical (N = 127), lumbosacral (N = 162), and other (N = 10). In contrast to limb onset, bulbar‐onset patients more frequently demonstrated a pattern of normal or near normal needle electromyography (EMG) (p < .0001) and less frequently had abnormalities on EMG of TPSP (p = .002). Clinical or EDX diagnosis of sensory polyneuropathy was present in 12.6% patients, more frequently in the lumbosacral onset subgroup (p < .03). EMG showed active denervation in 9.6% and chronic denervation in 59% of craniobulbar muscles examined, without observed difference among different onset regions. TPSP showed higher frequencies of active and chronic denervation in ALS than a group of patients with non‐ALS neuromuscular disorders.
Discussion
EDX features may differ among ALS patients of different onset regions. TPSP EMG is highly useful in differentiating ALS from non‐ALS neuromuscular disorders while the yield of craniobulbar muscles, especially for active denervation, is low.