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Establishment of a new treatment for dural arteriovenous fistula based on angiogenic factors

Research Project

Project/Area Number 16K19994
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Neurosurgery
Research InstitutionUniversity of Tsukuba (2017-2018)
National Cardiovascular Center Research Institute (2016)

Principal Investigator

Ito Yoshiro  筑波大学, 附属病院, 病院講師 (90733014)

Research Collaborator Watanabe Daisuke  
Takigawa Tomoji  
Sato Masayuki  
Marushima Aiki  
Tsuruta Wataro  
Hayakawa Mikito  
Takano Shingo  
Ishikawa Eiichi  
Matsumaru Yuji  
Matsumura Akira  
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Keywords血管新生因子 / 硬膜動静脈瘻 / 血管新生抑制療法
Outline of Final Research Achievements

Although the animal model was constructed by anastomizing the jugular vein and the internal carotid artery and occluding the sinus, it was difficult to find out the possibility of medical treatment in animal experiments. The blood of the lesion in the case of dural arteriovenous fistula was collected to verify the expression of angiogenic factors. The expression of angiogenic factors in the lesion was comprehensively measured using the antibody array kit. In the cavernous sinus lesions, the expression of VEGF-R3, IL1β, MMP9, and uPAR was suppressed in Aggressive type compared to Benign type. No factor was found to be upregulated in either Aggressive type or Benign type.

Academic Significance and Societal Importance of the Research Achievements

硬膜動静脈瘻の疾患発生と病態進行には従来考えられていた血管新生因子の高発現だけが関与するのではなく、血管新生因子の発現抑制や抑制系因子の発現が関与することを明らかにした。
関連した血管新生因子を定量的解析することで、硬膜動静脈瘻の発生や進行に関与している血管新生因子を同定することができる。さらには関与している血管新生因子に対する治療を行うことでこれまでは血管内治療では難治であった症例に対しても内科治療が奏功する可能性がある。

Report

(4 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (2 results)

All 2017 2016

All Presentation (2 results)

  • [Presentation] 海綿静脈洞部硬膜動静脈瘻における血管新生関連因子の解析2017

    • Author(s)
      渡部大輔、伊藤嘉朗、滝川知司、丸島愛樹、鶴田和太郎、早川幹人、高野晋吾、石川栄一、松丸祐司、松村明
    • Organizer
      第33回NPO法人脳神経血管内治療学会学術総会
    • Related Report
      2017 Research-status Report
  • [Presentation] 罹患静脈洞の血管新生因子の解析による硬膜動静脈瘻の病態解明2016

    • Author(s)
      伊藤嘉朗
    • Organizer
      軽井沢セミナー
    • Place of Presentation
      軽井沢プリンス
    • Year and Date
      2016-07-17
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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