Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis

Kazuaki Kanai, Kazumoto Shibuya, Yasunori Sato, Sonoko Misawa, Saiko Nasu, Yukari Sekiguchi, Satsuki Mitsuma, Sagiri Isose, Yumi Fujimaki, Shigeki Ohmori, Shunsuke Koga, Satoshi Kuwabara

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

Objective: The aim of this study was to investigate whether axonal excitability indices are associated with survival in patients with amyotrophic lateral sclerosis (ALS). Previous nerve excitability studies suggested increased persistent sodium currents in motor axons of patients with ALS, which lead to axonal hyperexcitability and potentially enhance neuronal death. Methods: 112 patients with sporadic ALS were followed up until endpoint (death or tracheostomy). Multivariate analyses were performed using the Cox proportional hazard model. Threshold tracking was used to measure multiple axonal excitability indices in median motor axons, such as strengtheduration time constant (SDTC; a measure of nodal persistent sodium current). Latent addition was also used to estimate the magnitude of persistent sodium currents. Results: The overall median tracheostomy-free survival from onset was 37 months. Prolonged SDTC was strongly associated with shorter survival (adjusted HR 4.07; 95% CI 1.7 to 9.8; p=0.0018) compared with older onset age (>60 years; HR=1.80) and bulbar onset (HR=1.80). Estimated median survival was 34 months in the longer SDTC group and 51 months in the shorter SDTC group. This index was highly statistically significant even after multiple testing adjustments with age and site of onset (bulbar or limb). Latent addition study results were consistent with these findings. Conclusions: Axonal persistent sodium currents, estimated by SDTC and latent addition, are strong and independent predictors for shorter survival in patients with ALS. Membrane hyperexcitability is possibly associated with motor neuronal death, and modulation of excessive sodium currents could be a novel therapeutic option for ALS.

Original languageEnglish
Pages (from-to)734-738
Number of pages5
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume83
Issue number7
DOIs
Publication statusPublished - 2012 Jul 1
Externally publishedYes

Fingerprint

Amyotrophic Lateral Sclerosis
Sodium
Survival
Tracheostomy
Age of Onset
Axons
Proportional Hazards Models
Multivariate Analysis
Extremities
sarcosine dithiocarbamate
Membranes

ASJC Scopus subject areas

  • Surgery
  • Clinical Neurology
  • Psychiatry and Mental health

Cite this

Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis. / Kanai, Kazuaki; Shibuya, Kazumoto; Sato, Yasunori; Misawa, Sonoko; Nasu, Saiko; Sekiguchi, Yukari; Mitsuma, Satsuki; Isose, Sagiri; Fujimaki, Yumi; Ohmori, Shigeki; Koga, Shunsuke; Kuwabara, Satoshi.

In: Journal of Neurology, Neurosurgery and Psychiatry, Vol. 83, No. 7, 01.07.2012, p. 734-738.

Research output: Contribution to journalArticle

Kanai, K, Shibuya, K, Sato, Y, Misawa, S, Nasu, S, Sekiguchi, Y, Mitsuma, S, Isose, S, Fujimaki, Y, Ohmori, S, Koga, S & Kuwabara, S 2012, 'Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis', Journal of Neurology, Neurosurgery and Psychiatry, vol. 83, no. 7, pp. 734-738. https://doi.org/10.1136/jnnp-2011-301782
Kanai, Kazuaki ; Shibuya, Kazumoto ; Sato, Yasunori ; Misawa, Sonoko ; Nasu, Saiko ; Sekiguchi, Yukari ; Mitsuma, Satsuki ; Isose, Sagiri ; Fujimaki, Yumi ; Ohmori, Shigeki ; Koga, Shunsuke ; Kuwabara, Satoshi. / Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis. In: Journal of Neurology, Neurosurgery and Psychiatry. 2012 ; Vol. 83, No. 7. pp. 734-738.
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AU - Nasu, Saiko

AU - Sekiguchi, Yukari

AU - Mitsuma, Satsuki

AU - Isose, Sagiri

AU - Fujimaki, Yumi

AU - Ohmori, Shigeki

AU - Koga, Shunsuke

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