4.7 Article

Association of Cortical Hyperexcitability and Cognitive Impairment in Patients With Amyotrophic Lateral Sclerosis

Journal

NEUROLOGY
Volume 96, Issue 16, Pages E2090-E2097

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000011798

Keywords

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Funding

  1. Motor Neuron Disease Research Institute of Australia
  2. Stanford Family MND Research Grant [GIA 1726]
  3. Innovator Grant [IG1960]
  4. National Health and Medical Research Council of Australia (NHMRC) [GNT1123026, 037746, 1153439, 1156093, MRF1154676]

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This study found that cortical hyperexcitability was more pronounced in cognitively impaired patients with ALS, indicating a potential association between cognitive impairment and TDP-43 accumulation. Reduced SICI was evident in ALS patients, especially in those with decreased executive function scores.
Objective To determine whether cortical hyperexcitability was more prominent in cognitively impaired patients with amyotrophic lateral sclerosis (ALS). Methods Threshold tracking transcranial magnetic stimulation (TMS) was used to assess cortical excitability and cognitive function was determined by the Edinburgh Cognitive and Behavioural ALS Screen (ECAS). Cognitive impairment was defined by ECAS < 105. Patients with ALS, defined by the Awaji criteria, were prospectively recruited. Patients unable to undergo TMS, or in whom TMS indices were compromised by coexistent medical conditions, were excluded. Cortical hyperexcitability was defined by reduced short interval intracortical inhibition (SICI) and increased short interval intracortical facilitation (SICF), index of excitability (IE), and motor evoked potential (MEP) amplitude. Student t test determined differences between groups and multivariable regression modeling was used to assess association among cognitive, clinical, and TMS measures. TMS results were compared with those of 42 controls. Results Cognitive impairment was evident in 36% of the 40 patients with ALS (23 male, mean age 62.1 years). Cortical hyperexcitability was more prominent in cognitively impaired patients as indicated by an increase in SICF (ECAS(>= 105) -15.3 +/- 1.7%, ECAS(<105) -20.6 +/- 1.2%; p < 0.01), IE (ECAS(>= 105) 80.9 +/- 7.8, ECAS(<105) 95.0 +/- 4.5; p < 0.01), and MEP amplitude (ECAS(>= 105) 28.7 +/- 3.3%, ECAS(<105) 43.1 +/- 5.9%; p < 0.05). SICF was independently associated with the ECAS score (beta = 2.410; p < 0.05). Reduced SICI was evident in ALS, being more prominent in patients with reduced executive score (ECAS(executive score>33) 6.2 +/- 1.3%, ECAS(executive score<33) 1.5 +/- 2.1%; p < 0.01). Conclusion Cortical hyperexcitability was more prominent in cognitively impaired patients with ALS than in controls. Given that ECAS is a valid predictor of TDP-43 pathology, the increase in cortical hyperexcitability may be associated with TDP-43 accumulation.

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