Non-motor multiple system atrophy associated with sudden death: pathological observations of autonomic nuclei

Yuichi Riku, Hirohisa Watanabe, Maya Mimuro, Yasushi Iwasaki, Mizuki Ito, Masahisa Katsuno, Gen Sobue, Mari Yoshida

研究成果: ジャーナルへの寄稿学術論文査読

15 被引用数 (Scopus)

抄録

Multiple system atrophy (MSA) manifests as a combination of dysautonomia and motor symptoms/signs. However, rare cases presenting with autonomic failures in absence of motor symptoms/signs until their deaths have been reported and are referred to as non-motor MSA. To clarify pathological findings underlying non-motor MSA patients, we analyzed consecutively autopsied 161 patients with MSA. In results, four patients were identified as having non-motor MSA, who showed isolated autonomic disorders throughout their lives and had minimal pathological changes in the motor systems. We also identified two patients with pathologically minimal MSA, who had minimal pathological involvement in the motor systems and presented with definite parkinsonism and dysautonomia. Survival durations of the non-motor MSA patients were much shorter (1.3–2.0 years) than those of the classical MSA patients (3.0–7.0 years), and the causes of death were all sudden death. The medullary serotonergic neurons were severely involved in the non-motor MSA patients in comparison with the classical MSA patients. Also, one of the pathologically minimal MSA patients had died suddenly and exhibited marked involvement of the medullary serotonergic neurons. The involvement of the medullary catecholaminergic or cholinergic neurons did not differ in severities among the groups. We conclude that non-motor MSA may be a pathological variant of MSA that preferentially involves the medullary serotonergic neurons and autonomic systems in association with poor prognosis.

本文言語英語
ページ(範囲)2249-2257
ページ数9
ジャーナルJournal of Neurology
264
11
DOI
出版ステータス出版済み - 01-11-2017
外部発表はい

All Science Journal Classification (ASJC) codes

  • 神経学
  • 臨床神経学

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