論文

査読有り 国際誌
2022年3月2日

Ultrasonographic evaluation reveals thinning of cervical nerve roots and peripheral nerves in spinal and bulbar muscular atrophy.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
  • Daisuke Watanabe
  • Hiroshi Tsukamoto
  • Tatsuya Abe
  • Ruriko Kitao
  • Aya Okuma
  • Masatoshi Mihara
  • Atsuko Katsumoto
  • Yukiko Iwahashi
  • Yuichi Higashiyama
  • Yosuke Miyaji
  • Hideto Joki
  • Hiroshi Doi
  • Tetsuo Komori
  • Fumiaki Tanaka
  • 全て表示

43
7
開始ページ
4267
終了ページ
4274
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s10072-022-05969-1

BACKGROUND: Ultrasonography (US) is a noninvasive and patient-friendly tool for the evaluation of peripheral nerves. In motor neuron diseases, amyotrophic lateral sclerosis (ALS) has been reported to show the atrophy of peripheral nerves on US. However, the US findings are still unclear in spinal and bulbar muscular atrophy (SBMA), an adult-onset lower motor neuron disease caused by an abnormal CAG repeat expansion in the androgen receptor gene. METHODS: We prospectively recruited and evaluated 11 patients with genetically confirmed SBMA and 9 patients with ALS diagnosed according to the revised El Escorial ALS criteria or the Awaji electrodiagnostic criteria. The C5-C7 cervical nerve roots and the median and ulnar nerves were evaluated ultrasonographically. RESULTS: The cross-sectional areas (CSAs) of the C6 and C7 nerve roots, the median nerve in the upper arm and forearm, and the ulnar nerve in the upper arm were smaller in patients with SBMA than those in patients with ALS (p < 0.05), whereas the CSAs of the C5 nerve root and the ulnar nerve in the forearm were not smaller. CONCLUSIONS: US showed that the peripheral nerves in patients with SBMA were thinner than those in patients with ALS despite similar degrees of weakness and motor neuron loss. Possible causes include additional sensory nerve involvement and longer disease duration in patients with SBMA than those in patients with ALS.

リンク情報
DOI
https://doi.org/10.1007/s10072-022-05969-1
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/35237894
ID情報
  • DOI : 10.1007/s10072-022-05969-1
  • PubMed ID : 35237894

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