• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Molecular biological analysis of emphysema heterogeniety and treatment response in patients with chronic obstructive pulmonary disease

Research Project

Project/Area Number 16K09593
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Respiratory organ internal medicine
Research InstitutionKanazawa Medical University

Principal Investigator

MIZUNO Shiro  金沢医科大学, 医学部, 教授 (80397281)

Co-Investigator(Kenkyū-buntansha) 石崎 武志  金沢医科大学, 医学部, 教授 (80151364)
Research Collaborator ANZAI Masaki  
KADOWAKI Maiko  
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords気腫多様性 / 気道可逆性 / ADRB2遺伝子 / ADR2遺伝子変異 / ADRB2遺伝子変異 / p53 / 血管内皮前駆細胞 / エクソソーム
Outline of Final Research Achievements

Our data demonstrated that the emphysema distribution and heterogeneity between the upper and lower lung could affect the BDR. ADRB2 Arg16Gly genotypes in COPD patients may predict the BDR to a short-acting β2-agonist in patients with upper lung dominant emphysema. Individualized therapeutic strategies based on the heterogeneity of emphysema distribution and genetic analysis of ADRB2 Arg16Gly polymorphism may play a key role in the treatment of COPD with β-adrenergic agonists. However, additional study to assess treatment of COPD patients classified by ADRB2 genotype with long acting β-adrenergic agonists will be necessary to confirm the clinical value of the utility of measurement of EHI% and ADRB2 Arg16Gly polymorphism in the treatment of COPD patients.

Academic Significance and Societal Importance of the Research Achievements

COPDの治療の中心である気管支拡張剤は、気腫病変の構造的違いやCOPDのフェノタイプの違いにより気管支拡張剤の効果が異なる群が混在し、COPD患者群の病態解析には形態学的異常と遺伝的素因の両者をカテゴライズし分析する必要があると考えられる。また気管支拡張剤による気道可逆性が診断根拠の一つに用いられる気管支喘息とCOPDの合併(Asthma COPD overlap syndrome: ACOS)にも、同病態が深く関与していることが想定される。

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

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (1 results)

  • [Journal Article] ADRB2 gene polymorphism and emphysema heterogeneity can modulate bronchodilator response in patients with emphysema2017

    • Author(s)
      Nojiri M, Mizuno S, Nishiki K, Kato R, Nakagawa K, Oikawa T, Iguchi M, Osanai, K, Ishizaki T, Toga H.
    • Journal Title

      Pulm Pharmacol Ther

      Volume: 48 Pages: 80-87

    • DOI

      10.1016/j.pupt.2017.09.004

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Presentation] COPDにおけるADRB2遺伝子多型と気腫性病変の分布の検討2017

    • Author(s)
      野尻正史、水野史朗、佐久間貴士、西木一哲、中瀬啓介、加藤諒、四宮祥平、高原豊、齋藤雅俊、小島好司、及川卓、中川研、長内和弘、栂博久
    • Organizer
      第57回日本呼吸器学会学術講演会
    • Place of Presentation
      東京国際フォーラム(東京都千代田区)
    • Year and Date
      2017-04-22
    • Related Report
      2016 Research-status Report

URL: 

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

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi