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2001 Fiscal Year Final Research Report Summary

Urease-pretreatment, stable isotope dilution and gas chromatographic mass spectrometrie application for the chemical diagnosis of inborn errors of metabolism

Research Project

Project/Area Number 11672312
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Laboratory medicine
Research InstitutionKanazawa Medical University

Principal Investigator

KUHARA Tomiko  Kanazawa Medical University, Div. of Human Genetics, Medical Research Institute, Professor, 総合医学研究所, 教授 (30080568)

Co-Investigator(Kenkyū-buntansha) INOUE Yoshito  Kanazawa Medical University, Div. of Human Genetics, Medical Research Institute, Associate Professor, 総合医学研究所, 講師 (20080616)
SHINKA Toshihiro  Kanazawa Medical University, Div. of Human Genetics, Medical Research Institute, Associate Professor, 総合医学研究所, 助教授 (10098858)
Project Period (FY) 1999 – 2000
KeywordsGC / MS / Inborn error of metabolism / chemical diagnosis / pyrimidine degradation / homocystinuria / Pilot study of neonatal screening / folate deficiency / Propionic acidemia
Research Abstract

1. In pyrimidine degradation three enzymes, PDH, DHP and UPase, are involved. In these enzyme deficiecies, pyrimidine analogues used for cancer chemotherapy cause serious side-effects. To prevent such severe side-effects, we developed a method by which specific, rapid and sensitive chemical diagnosis can made In "Modern Drug Discovery" published by American Chemical Society evaluated our method in "News in Brief".
2. Using urease-pretreatment, stable isotope dilution and GC/MS, we established a method to make differential chemical diagnosis of homocystinuria. We also confirmed that this method also detect folate deficiency secondarily caused by homocystinuria type I.
3. In the pilot study of neonatal screening, propionic acidemia )PCCD) and α-ketoadipic aciduria were found to occure 1 to 10,000〜20,000 babies. To detect mild type PCCD was supposed to be rather difficult in MS/MS using blood spots (J. Inher. Metab. Dis., (in press)).

  • Research Products

    (33 results)

All Other

All Publications (33 results)

  • [Publications] 浦澤林太郎: "急激な意識障害で発症したβ-ケトチオラーゼ欠損症の1乳児例"日小誌. 103・8. 849-852 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Peng: "Asymptomatic a -ketoadipic aciduria detected during a pilot study of neonatal urine screening"Acta Paediatr. 88. 911-914 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara: "Pilot study of gaschromatography-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease"J.Chromatogr.B. 731. 141-147 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Shinka: "Urine screening of five-day-old newborns: metabolic profiling of neonatal galactosuria"J.Chromatogr.B. 732. 469-477 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 井上義人: "GC/MSを用いた栄養性ピオチン欠乏症の化学診断"金医大総合医学研究所年報. 10. 137-146 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 久原とみ子: "尿GC/MS分析による代謝異常症例の化学診断および追跡調査"厚生科学研究(子ども家庭総合研究事業)(効果的なマススクリーニングの施策に関する研究)平成10年度研究報告書. 369-370 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara: "Differential Diagnosis of Homocystinuria by Urease-treatment, isotope-dilution and gas chromatography-mass spectrometry"J.Chromatogr.B. 742. 59-70 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 久原とみ子: "質量分析-新しい臨床検査への展開有機酸の代謝異常"臨床検査. 44・1. 57-67 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 石田志門: "巨赤芽球性貧血を合併したホモシスチン尿症の1例"日内誌. 89・12. 2528-2530 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 久原とみ子: "簡易尿ウレアーゼ法による有機酸血症のスクリーニング-プロピオン酸血症、メチルマロン酸血症を中心に-"厚生科学研究(子ども家庭総合研究事業)(効果的なマススクリーニングの実施に関する研究)平成11年度研究報告書. 386-388 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara: "Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography-mass spectrometry"J.Chromatogr.B. 758. 3-25 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara: "Simple gas chromatographic-mass spectrometric procedure for diagnosing Dyrimidine degradation defects for prevention of severe anticancer side effects"I.Chromatogr.B. 758. 61-74 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Miyamoto: "Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X"J.Hum.Genet.. 45. 260-262 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] S.Ishida: "Homocystinuria due to cystathionine β-synthase deficiency associated with megaloblastic anaemia"J.Int.Med.. 250. 453-456 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 加藤繁夫: "大脳皮質の萎縮を認めた Hyperornithinemia-Hyperammonemia-Homocitrullinuria(HHH)Syndromeの中年女性例"東邦医学会雑誌. 48・3. 271-278 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara: "Gas chromatographic-mass spectrometric newborn screening and diagnosis of propionic acidemia by Iargeting methylcitrate in dried filter-paper urine samples"J.Inher.Metab.Dis. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Shinka: "Rapid and sensitive detection of urinary 4-hydroxybutyric acid and it related compounds by GC(MS in a patient with succinic semialdehyde dehydrogenase deficiency"J.Chromatogr.B.. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Shinka: "Two cases of benign methylmalonic aciduria detected during a pilot study of neonatal urine screening"J.Chromatogr.B.. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Y.Inoue: "A Rapid and Sensitive Method for Prenatal Diagnosis of Propionic Acidemia Using Stable Isotope DilutionGC-MS and Urease Pretreatment"J.Chromatogr.B.. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] T.Kuhara et al.guest editors: "J.Chromatogr.B.Proceedings of 23rd Annual Meeting of the Japanese Society of Biomedical Mass Spectrometry, Kanazawa, Japan,24-26 September 1998"ELSEVIER. 114 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Peng.H.: "Asymptomatic α-ketoadipic aciduria detected during pilot study of neonatal urine screening"Acta Paediatr.. 88. 911-914 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuhara,T.: "Pilot study of gas chromatography-mass spectrometric screening of newborn urine for inborn errors of metabolism after treatment with urease."J. Chromatogr. B.. 731. 141-147 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shinka,T.: "Urine screening of five-day-old newborns: metabolic profiling of neonatal galactosuria"J. Chromatogr. B.. 732. 469-477 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuhara,T.: "Differential Diagnosis of Homocystinuria by Urease-treatment, isotope-dilution and gas chromatography-mass spectrometry"J. Chromatogr. B.. 742. 59-70 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuhara,T.: "Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas phromatography-mass spectrometry."J. Chromatogr. B.. 758. 3-25 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuhara,T.: "Simple gas chromatographic-mass spectrometric procedure for diagnosing pyrimidine degradation defects for prevention of severe anticancer side effects"J. Chromatogr. B.. 758. 61-74 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Miyamoto,T.: "Diagnosis of Japanese patients with HHH syndnome by molecular genetic analysis: a common mutation, R179X"J. Hum. Genet.. 46. 260-262 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishida,S.: "Homocystinuria due to cystathionine β-synthase deficiency associated with megaloblastic anaemia"J. Int. Med.. 250. 453-456 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuhara,T.: "Gas chromatographic-mass spectrometric newborn screening and diagnosis of propionic acidemia by targeting methylcitrate in dried filter-paper urine samples"J. Inher. Metab. Dis.. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shinka,T.: "Rapid and sensitive detection of urinary 4-hydroxybutyric acid and it related compounds by GC/MS in a patient with succinic semialdehyde dehydrogenase deficiency"J. Chromatogr. B.. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shinka,T.: "Two cases of benign methylmalonic aciduria detected during a pilot study of neonatal urine screening"J. Chromatogr. B.. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Inoue,Y.: "A Rapid and Sensitive Method for Prenatal Diagnosis of Propionic Acidemia Using Stable Isotope Dilution GC-MS and Urease Pretreatment"J. Chromatogr. B.. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Guest Editors: Kuhara,T.: "Proceedings of 23rd Annual Meeting of the Japanese Society of Biomedical Mass Spectrometry, Kanazawa, Japan, 24-26 September 1998"J. Chromatogr. B. 1-165, 1999 ELSEVIER, Amsterdam.

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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