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Basic study on the relationship between Kawasaki Disease and oral microbiota

Research Project

Project/Area Number 16K11865
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Social dentistry
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

Kita Masakazu  京都府立医科大学, 医学(系)研究科(研究院), 特任教授 (60153087)

Co-Investigator(Kenkyū-buntansha) 山本 俊郎  京都府立医科大学, 医学(系)研究科(研究院), 講師 (40347472)
金村 成智  京都府立医科大学, 医学(系)研究科(研究院), 准教授 (70204542)
池田 和幸  京都府立医科大学, 医学(系)研究科(研究院), 助教 (30507786)
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords川崎病 / 口腔細菌 / 免疫学 / 社会医学 / 口腔由来細胞 / トランスレーショナルリサーチ / 口腔由来細菌 / 細菌
Outline of Final Research Achievements

Kawasaki disease (KD) is a childhood vasculitis often associated with cardiovascular complications, including coronary artery aneurysms. Although its etiologic mechanisms are unknown, several studies indicate that dysregulated innate immune responses to external and internal microorganisms may be involved in the pathogenesis. The purpose of this study is to analyze dental microbiota of KD patients by metagenomic analysis, and identify specific microbiota in relation to the pathogenesis of acute-phase KD. In random forest analysis, Haemophilus spp. and TM7 were detected as bacterial species which could distinguish KD patients from healthy controls. Our studies revealed that a few microbiota was significantly decreased in KD patients, and this phenomenon is seems to be microbial dysbiosis. It has been speculated that dysbiosis would disrupt the balance of immune system, and trigger the onset of various immune diseases. Similar mechanism could be involved in the pathogenesis of KD.

Academic Significance and Societal Importance of the Research Achievements

川崎病は現在でも小児の 後天性心疾患の原因としてトップに位置しており、第24回川崎病全国調査では、2015年に患者数が過去最高を更新している。また、川崎病は心筋梗塞等の合併症を引き起こし、死に至ることもあるため、我が国の少子高齢化現象のなかで大きな問題となっている。本研究により川崎病の起炎菌が明らかになれば、それに有効な予防法・治療法の開発へとつながるため社会的意義は大きいと考えられる。

Report

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

    (5 results)

All 2019 2018 2017

All Presentation (5 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] メタゲノム解析を用いた川崎病患者口腔内バイオフィルム研究2019

    • Author(s)
      池田和幸・濱岡秀樹・岡本亜希子・足立哲也・鈴木千夏・八幡倫代・中村明宏・山本俊郎・金村成智・濵岡建城
    • Organizer
      第55回(特非)日本小児循環器学会総会・学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Characterization of the dental microbiota of Kawasaki disease by metagenomics analysis.2018

    • Author(s)
      Ikeda K, Okamoto-Hamaoka A, Hamaoka H, Tetsuya A, Yahata T, Suzuki C, Taniguchi M, Yamamoto T, Kanamura N, Hamaoka K
    • Organizer
      The 12th international Kawasaki disease symposium
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 川崎病発症原因菌としての口腔内バイオフィルム細菌に関するメタゲノム解析2018

    • Author(s)
      濵岡秀樹・池田和幸・足立哲也・山本俊郎・谷口誠・岡本亜希子・濵岡建城・金村成智
    • Organizer
      第148回(特非)日本歯科保存学会2018年度春季大会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 川崎病患者歯垢検体を用いた口腔内バイオフィルム研究2018

    • Author(s)
      池田和幸・濱岡秀樹・岡本亜希子・足立哲也・鈴木千夏・八幡倫代・中村明宏・山本俊郎・金村成智・濵岡建城
    • Organizer
      第38回(公社)日本川崎病学会・学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] 川崎病患者歯垢検体を用いた急性期病態におけるdysbiosisに関する研究2017

    • Author(s)
      池田和幸、岡本亜希子、濱岡秀樹、足立哲也、鈴木千夏、八幡倫代、中村明宏、谷口誠、山本俊郎、喜多正和、金村成智、濱岡建城
    • Organizer
      第37回日本川崎病学会
    • Related Report
      2017 Research-status Report

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

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