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DOI 10.1080/21678421.2017.1321676

Медицинская библиотека · Amyotrophic lateral sclerosis & frontotemporal degeneration · 2017

Impairment of triad conditioned facilitation in amyotrophic lateral sclerosis.

Groiss Stefan J, Mochizuki Hitoshi, Hanajima Ritsuko, Trenado Carlos, Nakatani-Enomoto Setsu, Otani Koji, Ugawa Yoshikazu

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

The triad conditioned facilitation (TCF) technique has been shown to detect motor cortical intrinsic rhythms depending on the functioning of specific cortical layers by measuring motor evoked potential (MEP) enhancement after a triad of conditioning TMS pulses at a certain interval. However, the influence of cortical degeneration on TCF is still undetermined. We therefore studied TCF in patients with amyotrophic lateral sclerosis (ALS), a neurodegenerative disorder characterised by degeneration of the motor cortex.

METHODS

Thirteen patients with ALS and 11 age-matched disease control patients with cervical myelopathy (CM) or radiculopathy (CR) participated in the study. We studied short-interval intracortical inhibition (SICI), intracortical facilitation (ICF) and TCF using the paired-pulse and triad conditioned TMS paradigm.

RESULTS

TCF was significantly reduced in ALS patients compared to CM/CR patients, who had normal TCF. SICI and ICF did not differ between groups.

CONCLUSION

The absence of TCF with preserved SICI and ICF suggests changes in the intrinsic rhythm generation within the motor cortex due to cortical neurodegeneration in ALS patients. In contrast, TCF was normal in patents with CM/CR in whom the motor cortical intrinsic circuits are not involved. This technique may be valuable to differentiate patients with ALS from those with CM/CR.

Для цитирования: Groiss Stefan J, Mochizuki Hitoshi, Hanajima Ritsuko, Trenado Carlos, Nakatani-Enomoto Setsu, Otani Koji, Ugawa Yoshikazu. Impairment of triad conditioned facilitation in amyotrophic lateral sclerosis.. Amyotrophic lateral sclerosis & frontotemporal degeneration. 2017. DOI: 10.1080/21678421.2017.1321676.

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