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Research on spinocerebellar ataxia caused by mutations in elongases

Research Project

Project/Area Number 18K15441
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 52020:Neurology-related
Research InstitutionInstitute of Physical and Chemical Research (2020-2021)
Juntendo University (2019)
Tokyo Medical and Dental University (2018)

Principal Investigator

Ozaki Kokoro  国立研究開発法人理化学研究所, 生命医科学研究センター, 副チームリーダー (10754765)

Project Period (FY) 2018-04-01 – 2022-03-31
Project Status Completed (Fiscal Year 2021)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2021: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2020: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2019: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2018: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Keywords脊髄小脳変性症 / 脂質代謝異常 / 神経変性疾患 / 神経病理 / 遺伝性疾患 / 遺伝学 / 神経内科学 / 疫学 / 脂質代謝 / 小脳失調症 / 神経学 / 代謝性疾患
Outline of Final Research Achievements

We studied the neuropathological basis of spinocerebellar ataxia typ34, which is caused by ELOVL4, coding a very-long fatty acid elongating enzyme for the first time. We revealed the distinctive neuropathological features including marked neuronal loss in specific brain regions, which are very important not only in this disease but also general neurodegenerative disorders. We published this work in [Ozaki et al., Acta Neuropathologica Commun 2021].
We also revealed disease frequency of SCA34 in an ataxia cohort in Japan. We described the clinical features in the pedigree and published in [Ozaki et al., Parkinsonism. Relat. Disord. 2019].

Academic Significance and Societal Importance of the Research Achievements

本研究ではSCA34という稀ながら非常に特徴のある神経変性疾患の患者さんを対象とした病理学的解析や、日本国内における患者さんの頻度調査を実施し、それぞれ一定の成果を挙げ、いずれも論文として国際誌に発表し。解析の結果では、非常に示唆に富んだ発見があり、脂質代謝異常に基づく本疾患の病態解明に資するのみならず、比較的頻度の高い疾患である進行性核上性麻痺という別の疾患に似た病理学的な特徴もあり、今後さらに本研究を深めることでこれまで知られていなかった一般的な神経変性疾患(例えばアルツハイマー病やパーキンソン病など)の知見に繋がっていく可能性もある。

Report

(5 results)
  • 2021 Annual Research Report   Final Research Report ( PDF )
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (7 results)

All 2022 2021 2019 2018

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 1 results) Presentation (5 results)

  • [Journal Article] Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study2021

    • Author(s)
      Ozaki Kokoro、Irioka Takashi、Uchihara Toshiki、Yamada Akane、Nakamura Ayako、Majima Takamasa、Igarashi Susumu、Shintaku Hiroshi、Yakeishi Mayumi、Tsuura Yukio、Okazaki Yasushi、Ishikawa Kinya、Yokota Takanori
    • Journal Title

      Acta Neuropathologica Communications

      Volume: 9 Issue: 1 Pages: 172-172

    • DOI

      10.1186/s40478-021-01272-w

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort2019

    • Author(s)
      Kokoro Ozaki, Ayaka Ansai, Kouji Nobuhara, Toshihiko Araki, Takayuki Kubodera, Takashi Ishii, Miwa Higashi, Nozomu Sato, Kazumasa Soga, Hidehiro Mizusawa, Kinya Ishikawa, Takanori Yokota
    • Journal Title

      Parkinsonism & Related Disorders

      Volume: - Pages: 238-242

    • DOI

      10.1016/j.parkreldis.2019.05.019

    • Related Report
      2018 Research-status Report
    • Peer Reviewed
  • [Presentation] The neuropathology of SCA34: widespread vacuolar white matter degeneration w ith oligodendrogliopathy2022

    • Author(s)
      尾崎心、入岡隆、内原俊記、山田茜、中村綾子、馬嶋貴正、五十嵐奨、新宅洋、矢毛石真由美、津浦幸夫、岡﨑康司、石川欽也、横田隆徳
    • Organizer
      第63回日本神経病理学会総会学術研究会
    • Related Report
      2021 Annual Research Report
  • [Presentation] SCA34の病理報告:オリゴデンドロサイト異常と空胞性白質変性、PSP様タウ病理2022

    • Author(s)
      尾崎心、入岡隆、内原俊記、山田茜、中村綾子、延原幸嗣、馬嶋貴正、五十嵐奨、新宅洋、矢毛石真由美、津浦幸夫、岡﨑康司、石川欽也、横田隆徳
    • Organizer
      第63回日本神経学会学術大会
    • Related Report
      2021 Annual Research Report
  • [Presentation] 脂肪酸伸長酵素ELOVL4の変異による脊髄小脳失調症34型2019

    • Author(s)
      尾崎心, 安斉綾香, 延原幸嗣, 荒木俊彦, 久保寺隆行, 石井俊, 東美和, 曽我一将, 入岡隆,三井純,石浦浩之,辻省次,馬嶋貴正,土井宏,岡﨑康司,田中章景,水澤英洋, 石川欽也, 横田隆徳
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Research-status Report
  • [Presentation] SCA34の遺伝疫学2019

    • Author(s)
      尾崎心,安斉綾香,延原幸嗣,荒木俊彦,久保寺隆行,石井俊,東美和,佐藤望,曽我一将,水澤英洋,石川欽也,横田隆徳
    • Organizer
      第60回日本神経学会学術大会
    • Related Report
      2018 Research-status Report
  • [Presentation] 本邦におけるSCA34の遺伝疫学的調査2018

    • Author(s)
      尾崎心,安斉綾香,石井俊,東美和,佐藤望,大北倫,曽我一将,水澤英洋,石川欽也,横田隆徳
    • Organizer
      第59回日本神経学会学術大会
    • Related Report
      2018 Research-status Report

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Published: 2018-04-23   Modified: 2023-12-25  

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