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Assesment of auistic tarit in patients with muscular dystrophy and clinical psychological supports

Research Project

Project/Area Number 25380926
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Clinical psychology
Research InstitutionOsaka University

Principal Investigator

IMURA OSAMU  大阪大学, 人間科学研究科, 教授 (20176506)

Co-Investigator(Renkei-kenkyūsha) SAITO TOSHIO  国立病院機構刀根山病院, 臨床研究部, 医師 (60538776)
MATSMURA TSUYOSHI  国立病院機構刀根山病院, 臨床研究部, 医師 (30549366)
FUJIMURA HARUTOSHI  国立病院機構刀根山病院, 臨床研究部, 医師 (20263246)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords筋ジストロフィー / 自閉スペクトラム症(ASD) / PARS-SF / SRS / エクソン / アイソフォーム / ジストロフィン遺伝子 / 自閉傾向 / ジストロフィン異常 / 心理的支援 / 自閉的傾向 / 発達障害 / PARS / CNS障害
Outline of Final Research Achievements

The aim of this study was to investigate the association between the location of mutations in the dystrophin gene and autistic characteristics.Patients with dystrophinopathies (n = 56; mean age = 12.9, SD = 5.2) participated in this study. Autistic characteristics were assessed using PARS-SF and SRS.Eighteen patients (32.1%) showed autistic characteristics by the PARS-SF infantile rating, while 11 patients (19.6%) also scored above the cut-off value on the PARS-SF current rating. Two of seven patients (29%) with mutations in exon 30-44 and five of 25 patients (20%) with mutations in exon 45-55 exceeded the cut-off value in both the infantile and current ratings of PARS-SF, whereas none of the patients with mutations in the exons upstream of exon 30 did so.
We found significantly higher ASD characteristics in patients with mutations in exon 45-55 compared to patients with mutations upstream of exon 30.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (10 results)

All 2016 2015 2014 2013 Other

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Acknowledgement Compliant: 1 results) Presentation (7 results)

  • [Journal Article] A preliminary study on the evaluation of ADHD tendancy in children with DMD/BMD2015

    • Author(s)
      新垣ほのか、榎本聖香、井村修、藤野陽生、松村剛、齋藤利雄、藤村晴俊
    • Journal Title

      脳と発達

      Volume: 47 Pages: 306-306

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Characteristics of autistic behavior in patients with dystrophinopaties.2015

    • Author(s)
      Fujino, H., Saito, T., Matsumura, T., Shibata, S., Iwata, Y., Fujimura, H., Imura, O.
    • Journal Title

      脳と発達

      Volume: 47 Pages: 345-345

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed
  • [Journal Article] How Physicians Support Mothers of Children with Duchenne Muscular Dystrophy2015

    • Author(s)
      Fujino, H., Saito, T., Matsumura, T., Shibata, S., Iwata, Y., Fujimura, H., Shinno. S. & Imura, O.
    • Journal Title

      Journal of Child Neurology

      Volume: - Pages: 1-8

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] 筋強直性ジストロフィー患者における認知機能とQoLの関連の探索的検討2016

    • Author(s)
      藤野陽生、新垣ほのか、榎本聖香、井村修他13名
    • Organizer
      第2回筋ジストロフィーのCNS障害研究会
    • Place of Presentation
      東京大学弥生講堂
    • Year and Date
      2016-01-09
    • Related Report
      2015 Annual Research Report
  • [Presentation] 筋強直性ジストロフィー患者における注意機能、視空間認知機能の特徴2016

    • Author(s)
      上田幸彦、諏訪園秀吾、奥間めぐみ、井村修他13名
    • Organizer
      第2回筋ジストロフィーのCNS障害研究会
    • Place of Presentation
      東京大学弥生講堂
    • Year and Date
      2016-01-06
    • Related Report
      2015 Annual Research Report
  • [Presentation] 筋ジストロフィーにおける発達障害についての心理学的検討2015

    • Author(s)
      井村修
    • Organizer
      第57回日本小児神経学会
    • Place of Presentation
      大阪帝国ホテル
    • Year and Date
      2015-05-28
    • Related Report
      2015 Annual Research Report
  • [Presentation] DMD/BMD患児における社会的認知に関する研究2014

    • Author(s)
      松井美也子、藤野陽生、前田直子、船越愛絵、上野紘子、阪上由衣、齋藤利雄、松村剛、井村修
    • Organizer
      第56回日本小児神経学会学術集会
    • Place of Presentation
      アクトシティ浜松
    • Year and Date
      2014-05-30
    • Related Report
      2014 Research-status Report
  • [Presentation] DMD/BMD患者の広汎性発達障害傾向に関する調査研究―SRSを用いて2013

    • Author(s)
      前田直子,柴田早紀,岩田優子,藤野陽生,船越愛絵,齋藤利雄,松村剛,井村修
    • Organizer
      第55回日本小児神経学会
    • Place of Presentation
      大分市
    • Related Report
      2013 Research-status Report
  • [Presentation] DMD/BMD外来患者の広汎性発達障害傾向に関する調査研究―PARSを用いて2013

    • Author(s)
      船越愛絵,柴田早紀,岩田優子,藤野陽生,前田直子,齋藤利雄,松村剛,井村修
    • Organizer
      第55回日本小児神経学会
    • Place of Presentation
      大分市
    • Related Report
      2013 Research-status Report
  • [Presentation] 筋ジストロフィーにおける発達障害傾向の測定とその課題

    • Author(s)
      井村修,藤野陽生
    • Organizer
      第2回DystrophinopathyのCNS障害研究会
    • Place of Presentation
      東京都
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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