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Evaluation for genetic predisposition and clinical pathological stratification in cardiac sarcoidosis

Research Project

Project/Area Number 18K08071
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 53020:Cardiology-related
Research InstitutionOsaka University

Principal Investigator

Minamiguchi Hitoshi  大阪大学, 医学系研究科, 招へい教員 (90648495)

Co-Investigator(Kenkyū-buntansha) 坂田 泰史  大阪大学, 医学系研究科, 教授 (00397671)
朝野 仁裕  大阪大学, 医学系研究科, 講師 (60527670)
木岡 秀隆  大阪大学, 医学系研究科, 助教 (70642099)
Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2020: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2019: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywordsサルコイドーシス / 心臓サルコイドーシス / HLA / ゲノム
Outline of Final Research Achievements

Cardiac sarcoidosis defines the prognosis for sarcoidosis. In addition to the immunological genetic factors known for the development of cardiac sarcoidosis, we hypothesized that mutations in cardiomyopathy-related genes might be involved, and examined 78 cases of cardiac sarcoidosis in terms of both clinical information and genomic information. HLA typing was performed in 74 cases and cardiomyopathy-related genes in 73 cases. HLA-DQB1*06:01 possession was observed in 39 cases, but no association with cardiac dysfunction or conduction disorder was observed. On the other hand, cardiomyopathy-related genes were found in 8 cases, and there is a possibility that the genes are significantly retained in patients with decreased cardiac function. We plan to reexamine them by accumulating more cases in the near future.

Academic Significance and Societal Importance of the Research Achievements

サルコイドーシスは原因不明の肉芽腫性疾患である。サルコイドーシスの症状発現部位は、目、肺、心臓、消化管などが知られており、臨床像は多彩である。中でも心臓サルコイドーシスはサルコイドーシスの予後を規定する。重症化した心臓サルコイドーシスは特発性拡張型心筋症と病態が類似し、心臓移植以外の有効な治療法が存在しない。サルコイドーシスが重症化するメカニズムに関して、既知の免疫学的な遺伝要素に加え、心筋症関連遺伝子の変異が関与しているのではないかとの仮説をたて、その仮説を検証することで、重症化する症例の早期発見、介入に関する新たな手法の確立につながるものと考えられる。

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report

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Published: 2018-04-23   Modified: 2022-01-27  

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