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

Establishment of genetic diagnosis and medical treatment in patients with inborn errors of bile acid metabolism: Aiming to prevent liver transplantation

Research Project

Project/Area Number 22791008
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Pediatrics
Research InstitutionKurume University

Principal Investigator

MIZUOCHI Tatsuki  久留米大学, 医学部, 助教 (20368921)

Project Period (FY) 2010 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2012: ¥390,000 (Direct Cost: ¥300,000、Indirect Cost: ¥90,000)
Fiscal Year 2011: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords遺伝学 / 酵素 / 内科 / 移植・再生医療
Research Abstract

Inborn errors of bile acid metabolism (IEBAM) have symptoms of cholestasis in children and the prognosis is poor due to cirrhosis unless diagnosis is made and treatment is initiated at an early stage of cholestasis. It is important to diagnose and treat patients with IEBAM at an early stage of cholestasis because we can treat them with medical therapy if early. We diagnose patients with IEBAM by bile acid analysis using Gas Chromatography - Mass Spectrometry and genetic analysis using direct sequence. We diagnosed and have been treating 6 patients with IEBAM during this study period. We have been studying clinical course, liver function test, and bile acid analysis in all of them. Our study demonstrates that the early diagnosis and treatment in patients with IEBAS are useful because all of them have had good clinical course. We can treat the patients with IEBAS with oral chenodeoxycholic acid if we diagnose them at an early stage. It is necessary that pediatrician know IEBAM becuse IEBAM are very rare disease and the diagnosis need special examinations such as bile acid analysis and genetic analysis. Distinctive findings of IEBAM are normal serum concentration of γ-GTP and total bile acid; however children present with cholestasis. We presented this study at the meeting and congress associated with pediatric liver disease. Moreover, we reported this study as the articles in Japanese and English, and investigated the pathophysiology and treatment of IEBAM. Currently, we are writing a paper summarizing the study of IEBAM over the past few years.

Report

(4 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • Research Products

    (29 results)

All 2013 2012 2011 2010

All Journal Article (16 results) (of which Peer Reviewed: 16 results) Presentation (13 results)

  • [Journal Article] Two neonatal cholestsis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment.2013

    • Author(s)
      Seki, Y., Mizuochi, T., Kimura, A., Takahashi T., Ohtake, A., Hayashi, S., Morimura, T., Ohno, Y., Hoshina, T., Ihara, K., Takei, H., Nittono H., Kurosawa T., Homma K., Hasegawa T., Matsuishi T.
    • Journal Title

      J Inherit Metab Dis

      Volume: 36(3) Issue: 3 Pages: 565-573

    • DOI

      10.1007/s10545-012-9526-6

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Oxysterol changes along with cholesterol and vitamin D changes in adult phenylketonuric patients diagnosed by newborn mass-screening.2013

    • Author(s)
      Nagasaka H, Okano Y, Kimura A, Mizuochi T, Sanayama Y, Takatani T, Nakagawa S, Hasegawa E, Hirano K, Mochizuki H, Ohura T, Ishige-Wada M, Usui H, Yorifuji T, Tsukahara H, Hirayama S, Ohtake A, Yamato S, Miida T.
    • Journal Title

      Clin Chim Acta.

      Volume: 416 Pages: 54-9

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Two neonatal cholestasis patients with mutations in the SRD5B1 (AKR1D1) gene: diagnosis and bile acid profiles during chenodeoxycholic acid treatment2013

    • Author(s)
      Seki Yoshitaka, et al.
    • Journal Title

      Journal of Inherited Metabolic Disease

      Volume: in press

    • Related Report
      2012 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Detection of Δ4-3-oxo-steroid 5β-reductase deficiency by LC-ESI-MS/MS measurement of urinary bile acids.2012

    • Author(s)
      Muto A, Takei H, Unno A, Murai T, Kurosawa T, Ogawa S, Iida T, Ikegawa S, Mori J, Ohtake A, Hoshina T, Mizuochi T, Kimura A, Hofmann AF, Hagey LR, Nittono H.
    • Journal Title

      J Chromatogr B Analyt Technol Biomed Life Sci.

      Volume: 900 Pages: 24-31

    • DOI

      10.1016/j.jchromb.2012.05.023

    • Related Report
      2012 Annual Research Report 2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Neonatal cholestasis with increased3β-monohydroxy-Δ bile acids inserum and urine: not necessarilyprimary oxysterol7α hydroxylase deficiency.2012

    • Author(s)
      Kimura A, Nittono H, Mizuochi T,Ueki I, Kurosawa T, Muto A, Takei H.
    • Journal Title

      Clin Chim Acta.

      Volume: 413(19-20) Issue: 19-20 Pages: 1700-4

    • DOI

      10.1016/j.cca.2012.05.016

    • Related Report
      2012 Annual Research Report 2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Characterization of urinary bile acids in a pediatric BRIC-1 patient: Effectof rifampicin treatment.2012

    • Author(s)
      Mizuochi T., Kimura A., Tanaka A., Muto A., Nittono H., Seki Y., Takahashi T., Kurosawa T., Kage M., Takikawa H., Matsuishi T.
    • Journal Title

      Clin Chim Acta

      Volume: 413(15-16) Issue: 15-16 Pages: 1301-1304

    • DOI

      10.1016/j.cca.2012.04.011

    • Related Report
      2012 Annual Research Report 2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Oxysterol changes along with cholesterol and vitamin D changes in adult phenylketonuric patients diagnosed by newborn mass-screening2012

    • Author(s)
      Nagasaka Hironori, et al.
    • Journal Title

      Clinica Chimica Acta

      Volume: 416 Pages: 54-59

    • DOI

      10.1016/j.cca.2012.10.011

    • Related Report
      2012 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Successful heterozygous living donor liver transplantation for an oxysterol 7α-hydroxylase deficiency in a Japanese patient.2011

    • Author(s)
      Mizuochi T, Kimura A, Suzuki M, Ueki I, Takei H, Nittono H, Kakiuchi T, Shigeta T, Sakamoto S, Fukuda A, Nakazawa A, Shimizu T, Kurosawa T, Kasahara M.
    • Journal Title

      Liver Transpl

      Volume: 17(9) Issue: 9 Pages: 1059-65

    • DOI

      10.1002/lt.22331

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] 先天性胆汁酸代謝異常.2011

    • Author(s)
      水落建輝,木村昭彦
    • Journal Title

      小児内科

      Volume: 43 Pages: 1042-1045

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Zinc Monotherapy From Time of Diagnosis for Young Pediatric Patients With Presymptomatic Wilson Disease2011

    • Author(s)
      Mizuochi Tatsuki, et al
    • Journal Title

      J Pediatric Gastroenterology and Nutrition

      Volume: 53 Pages: 365-367

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Successful Heterozygous Living Donor Liver Transplantation for an Oxysterol7α-Hydroxylase Deficiency in a Japanese Patient2011

    • Author(s)
      Mizuochi Tatsuki, et al
    • Journal Title

      Liver Transplantation

      Volume: 17 Pages: 1059-1065

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 先天性胆汁酸代謝異常2011

    • Author(s)
      水落建輝, 他
    • Journal Title

      小児内科2011;43:1042-1045

      Volume: 43 Pages: 1042-1045

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Molecular genetics and bile acid profiles of 3beta-hydroxy-delta5-C27-steroid dehydrogenase/isomerase deficiency in 2 Japanise patients.2010

    • Author(s)
      Mizuochi T., Kimura A., Ueki I., Takahashi T., Hashimoto T., Takao A., Seki Y., Takei H., Nittono H., Kurosawa T., Matsuishi T.
    • Journal Title

      Pediatr Res

      Volume: 68(3) Pages: 258-263

    • DOI

      10.1203/00006450-201011001-00505

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] 胆汁酸代謝異常症-診断へのアプローチと1次胆汁酸療法-.2010

    • Author(s)
      水落建輝,木村昭彦
    • Journal Title

      小児科臨床

      Volume: 63 Pages: 2081-2087

    • Related Report
      2012 Final Research Report
    • Peer Reviewed
  • [Journal Article] Molecular Genetic and Bile Acid Profiles in Two Japanese Patients With 3β -Hydroxy-Δ^5-C_27-Steroid Dehydrogenase/Isomerase Deficiency.2010

    • Author(s)
      Mizuochi Tatsuki
    • Journal Title

      Pediatric Research

      Volume: 68巻 Pages: 258-263

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 胆汁酸代謝異常症-診断へのアプローチと1次胆汁酸療法-2010

    • Author(s)
      水落建輝
    • Journal Title

      小児科臨床

      Volume: 63巻 Pages: 2081-2087

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Presentation] Molecular genetics in Asian patients with inborn errors of bile acid synthesis.2012

    • Author(s)
      Tatsuki Mizuochi.
    • Organizer
      The 4th World Congress of Pediatric Gastroenterology, Hepatology and Nutrition. Oral Presentation.
    • Place of Presentation
      Taipei, Taiwan
    • Related Report
      2012 Final Research Report
  • [Presentation] 3β-HSD欠損症の邦人2例に対する分子遺伝学的解析と胆汁酸プロファイル.第39回日本小児栄養消化器肝臓学会・2012

    • Author(s)
      水落建輝
    • Organizer
      第29回日本小児肝臓研究会
    • Place of Presentation
      大阪
    • Related Report
      2012 Final Research Report
  • [Presentation] 胆汁酸代謝異常症.2012

    • Author(s)
      水落建輝
    • Organizer
      第115回日本小児科学会学術集会分野別シンポジウム「代謝性肝疾患の最前線」.
    • Place of Presentation
      福岡
    • Related Report
      2012 Final Research Report
  • [Presentation] 分野別シンポジウム「代謝性肝疾患の最前線」 胆汁酸代謝異常症2012

    • Author(s)
      水落建輝
    • Organizer
      第115回日本小児科学会学術集会
    • Place of Presentation
      福岡
    • Related Report
      2012 Annual Research Report
  • [Presentation] 3β-HSD欠損症の邦人2例に対する分子遺伝学的解析と胆汁酸プロファイル2012

    • Author(s)
      水落建輝
    • Organizer
      第39回日本小児栄養消化器肝臓学会・第29回日本小児肝臓研究会
    • Place of Presentation
      大阪
    • Related Report
      2012 Annual Research Report
  • [Presentation] Molecular genetics in Asian patients with inborn errors of bile acid synthesis2012

    • Author(s)
      Mizuochi Tatsuki
    • Organizer
      The 4th World Congress of Pediatric Gastroenterology, Hepatology and Nutrition
    • Place of Presentation
      Taipei, Taiwan
    • Related Report
      2012 Annual Research Report
  • [Presentation] 肝内胆汁うっ滞に対するリファンピシン作用機序の解析2011

    • Author(s)
      水落建輝
    • Organizer
      第28回日本小児肝臓研究会
    • Place of Presentation
      つくば国際会議場(茨城)
    • Year and Date
      2011-07-16
    • Related Report
      2011 Annual Research Report
  • [Presentation] 胆汁酸代謝異常症.2011

    • Author(s)
      水落建輝.
    • Organizer
      第53回日本先天代謝異常学会
    • Place of Presentation
      千葉
    • Related Report
      2012 Final Research Report
  • [Presentation] Oxysterol7α欠損症に対する遺伝子解析と生体肝移植-世界初の肝移植救命例の報告-.2011

    • Author(s)
      水落建輝
    • Organizer
      第114回日本小児科学会学術集会.
    • Place of Presentation
      東京
    • Related Report
      2012 Final Research Report
  • [Presentation] Oxysterol 7α欠損症に対する遺伝子解析と生体肝移植-世界初の肝移植救命例の報告-2011

    • Author(s)
      水落建輝
    • Organizer
      第114回日本小児科学会学術集会
    • Place of Presentation
      グランドプリンス新高輪(東京)
    • Related Report
      2011 Annual Research Report
  • [Presentation] 胆汁酸代謝異常症2011

    • Author(s)
      水落建輝
    • Organizer
      第53回日本先天代謝異常学会
    • Place of Presentation
      幕張メッセ(千葉)
    • Related Report
      2011 Annual Research Report
  • [Presentation] 新生児肝炎の鑑別疾患としての胆汁酸代謝異常症-本邦における診断法の確立-.2010

    • Author(s)
      水落建輝
    • Organizer
      第113回日本小児科学会学術集会.
    • Place of Presentation
      岩手
    • Related Report
      2012 Final Research Report
  • [Presentation] 新生児肝炎の鑑別疾患としての胆汁酸代謝異常症-本邦における診断法の確立-2010

    • Author(s)
      水落建輝
    • Organizer
      第113回日本小児科学会学術集会
    • Place of Presentation
      岩手
    • Related Report
      2010 Annual Research Report

URL: 

Published: 2010-08-23   Modified: 2019-07-29  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi