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Mlecular analysis of epigenetic disorders including pseudohypoparathyroidism

Research Project

Project/Area Number 26461392
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Endocrinology
Research InstitutionDepartment of Clinical Research, National Hospital Organization Kyoto Medical Center

Principal Investigator

Usui Takeshi  独立行政法人国立病院機構(京都医療センター臨床研究センター), 内分泌代謝高血圧研究部, 客員室長 (20271512)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords偽性副甲状腺機能低下症 / メチル化 / GNAS
Outline of Final Research Achievements

To clarify the usefulness of methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA), we evaluated genetic and epigenetic changes of the GNAS locus in Japanese PHP-Ib patients.
We studied 13 subjects with PHP-Ib (three families with eight affected members and one unaffected member and four sporadic cases). The methylation status of GNAS differentially methylated regions (DMRs) was evaluated using MS-MLPA. The main outcome measure was the presence of deletion mutations in the GNAS locus and STX16, which were assessed using MLPA. In all familial PHP-Ib cases, a 3kb deletion of STX16 and demethylation of the A/B domain were identified. In contrast, no deletion was detected throughout the entire GNAS locus region in the sporadic cases. Broad methylation abnormalities were observed in the GNAS DMRs.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (12 results)

All 2017 2016 2015 2014

All Journal Article (8 results) (of which Int'l Joint Research: 2 results,  Peer Reviewed: 8 results,  Open Access: 4 results) Presentation (4 results) (of which Invited: 1 results)

  • [Journal Article] Determinants of Glycated Hemoglobin in Subjects With Impaired Glucose Tolerance: Subanalysis of the Japan Diabetes Prevention Program.2017

    • Author(s)
      Sakane N, Sato J, Tsushita K, Tsujii S, Kotani K, Tominaga M, Kawazu S, Sato Y, Usui T, Kamae I, Yoshida T, Kiyohara Y, Sato S, Tsuzaki K, Nirengi S, Takahashi K, Kuzuya H, Group JR.
    • Journal Title

      J Clin Med Res.

      Volume: 7 Issue: 4 Pages: 360-365

    • DOI

      10.14740/jocmr2928w

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.2016

    • Author(s)
      Imashuku S, Muramatsu H, Sugihara T, Okuno Y, Wang X, Yoshida K, Kato A, Tatsumi Y, Hattori A, Kita S, Oe K, Sueyoshi A, Usui T, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Kanno H
    • Journal Title

      Int J Hematol

      Volume: 印刷中 Issue: 1 Pages: 125-129

    • DOI

      10.1007/s12185-016-1970-x

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] The impact of equol-producing status in modifying the effect of soya isoflavones on risk factors for CHD: a systematic review of randomised controlled trials.2016

    • Author(s)
      Birru RL, Ahuja V, Vishnu A, Evans RW, Miyamoto Y, Miura K, Usui T, Sekikawa A
    • Journal Title

      J Nutr Sci.

      Volume: 5 Pages: 1-21

    • DOI

      10.1017/jns.2016.18

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] ELEVATED LEVELS OF PLASMA IMMUNOASSAYABLE ALDOSTERONE IN A MILD FORM OF 17 ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY DIAGNOSED AT THE AGE OF 50.2015

    • Author(s)
      Yohei Ueda,Takeshi Usui,Tomokazu Watanabe,Keiichi Kaneko,Rieko Nakatani,Maiko-Kakita Kobayashi,Kanako Tanase-Nakao,Kazutaka Nanba,Mika Tsuiki,Tetsuya Tagami,Mitsuhide Naruse,Yuko Toyoda,KeikoHomma,Tomonobu Hasegawa,Akira Shimatsu
    • Journal Title

      AACE Clinical Case Reports

      Volume: 未定

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Journal Article] DENOSUMAB FOR THE TREATMENT OF REFRACTORY HYPERCALCEMIA IN METASTATIC PARATHYROID CARCINOMA2015

    • Author(s)
      Saori Itoshima,Akiko Yuno,Tomomi Kato,Hidetoshi Kamada,Akemi Ikota,Takeshi Usui,Akira Shimatsu,Shigeki Koizumi
    • Journal Title

      AACE Clinical Case Reports

      Volume: 1(No.1) Issue: 4 Pages: e65-e68

    • DOI

      10.4158/ep13424.cr

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Journal Article] A CASE OF C CELL HYPERPLASIA IN AN ASYMPTOMATIC V804M RET MUTATION CARRIER; CAN THE CALCIUM INFUSION TEST PREDICT C CELL HYPERPLASIA?2015

    • Author(s)
      Maiko-Kakita Kobayashi,Yohei Ueda,Kanako Tanase-Nakao,Takeshi Usui,Yoshiki Watanabe,Tetsuro Yamamoto,Kazutaka Nanba,Tetsuya Tagami,Mitsuhide Naruse,Ryo Asato,Akira Shimatsu
    • Journal Title

      AACE Clinical Case Reports

      Volume: 1(No.2)

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Journal Article] 18F-FDG-PET-positive adrenal tumour2015

    • Author(s)
      Maiko Kakita-Kobayashi,Takeshi Usui,Hironobu Sasano,Akira Shimatsu
    • Journal Title

      BMJ Case Reports

      Volume: 2015 Pages: 1-1

    • DOI

      10.1136/bcr-2015-209379

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] A 22-year-old Woman with Hypocalcemia and Clinical Features of Albright Hereditary Osteodystrophy Diagnosed with Sporadic Pseudohypoparathyroidism Type Ib Using a Methylation-specific Multiplex Ligation-dependent Probe Amplification Assay2014

    • Author(s)
      Satoshi Zeniya,Akiko Yuno,Takayuki Watanabe,Takeshi Usui,Yurie Moriki,Yoshitaka Uno,Hirotomo Miake
    • Journal Title

      INTERNAL MEDICINE

      Volume: 53 Pages: 979-986

    • NAID

      130004902965

    • Related Report
      2014 Research-status Report
    • Peer Reviewed
  • [Presentation] 21水酸化酵素欠損症の出生前診断、出生前治療の現状と問題点2016

    • Author(s)
      臼井 健
    • Organizer
      日本内分泌学会学術総会
    • Place of Presentation
      国立京都国際会館
    • Year and Date
      2016-04-20
    • Related Report
      2016 Annual Research Report
    • Invited
  • [Presentation] 偽性副甲状腺機能低下症の分子病態とエピゲノム2015

    • Author(s)
      臼井 健
    • Organizer
      日本内分泌学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2015-04-23
    • Related Report
      2015 Research-status Report
  • [Presentation] GNAS遺伝子上流のメチル化異常のみを認めた偽性副甲状腺機能低下症Iaの1例2015

    • Author(s)
      佐々木 介,宮崎 卓,山下 剛央,富田 明夫,河村 真実,河村 信利,中島 弘幸,河村 保男,臼井 健
    • Organizer
      第225回日本内科学会東海地方会
    • Place of Presentation
      津
    • Year and Date
      2015-02-22
    • Related Report
      2014 Research-status Report
  • [Presentation] 本邦における偽性副甲状腺機能低下症(PHP)-Ⅰのgenetic,epigenetic解析2014

    • Author(s)
      臼井健、湯野暁子、島津章
    • Organizer
      第59回日本人類遺伝学会 第21回日本遺伝子診療学会 合同大会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2018-03-22  

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