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Relationship between Steroid-induced Osteoporosis and the Polymorphisms of Glucocorticoid Receptor Gene

Research Project

Project/Area Number 12670749
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionOsaka University

Principal Investigator

NAKAJIMA Shigeo  Osaka University, Graduate School of Medicine, Assistant Professor, 医学系研究科, 助手 (30270771)

Co-Investigator(Kenkyū-buntansha) SHIMA Masaaki  Osaka University, Graduate School of Medicine, Lecturer, 医学系研究科, 講師 (10252660)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2001: ¥1,200,000 (Direct Cost: ¥1,200,000)
Keywordssteroid hormone / osteoporosis / glucocorticoid receptor / 11β-HSD / gene polymorphism / グルココルチコイド
Research Abstract

In order to investigate the genetic factors associated with the steroid-induced osteoporosis, we examined the polymorphisms of several genes, such as glucocorticoid receptor (GR) and 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2). DNA fragments containing polymorphic sites were amplified by PCR method using the putative priomer sets, and the DNA sequences were analyzed by the direct sequence method. Previously reported polymorphisms of GR gene (N363S) and 11β-HSD2 (G534A) were not found in 50 normal Japanese subjects nor 7 steroid-treated patients. We next searched SNPs in Japanese SNP data base. Three SNPs of GR gene and 2 of CYP3A4 gene, but none of 11β-HSD2 gene, were registered in the data base. Among them, we examined the SNPs of the GR gene (JST006606, 032069, 057143). Steroid-treated patient with C/T of JST006606 demonstrated the smaller decline of the bone mineral density than those in the patients with T/T.
JST032069 did not affect the extents of the decrease in the bone mineral density. In conclusion, the GR gene polymorphism may possibly affect the sensitivity to the steroid hormone in the Japanese population.

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report
  • Research Products

    (18 results)

All Other

All Publications (18 results)

  • [Publications] M.Akagi, K.Inui, S.Nakajima, et al.: "Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome"Journal of Human Genetics. 45. 60-62 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] A.Onda, M.Shima, S.Onoe, M.Hanada, T.Nagai, S Nakajima, et al.: "Botryoid Wilms tumor : case report and review of literature"Pediatric Nephrology. 14. 59-61 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] S.Nakajima, et al.: "Effect of cyclic adenosine 3',5'-monophosphate and protein kinase A on ligand-dependent transactivation via the vitamin D receptor"Molecular and Cellular Endocrinology. 159. 45-51 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] S.Matsumoto, S.Nakajima, et al.: "Interferon treatment on glomerulonephritis associated with hepatitis C virus"Pediatric Nephrology. 15. 271-273 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] H.Hirai, S.Nakajima, et al.: "A novel activating mutatiol (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia"Journal of Human Genetics. 46. 41-44 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] T.Kubota, H.Hirai, N.Shimizu, A.Sawada, H.Kondou, S.Nakajima, et al.: "Development of hyperthyroidism in a patient with idiopathic nephrotic syndrome"Pediatric Nephrology. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] M. Akagi, K. Inui, S. Nakajima. et al: "Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome"Journal of Human Genetics. 45. 60-62 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] A. Honda, M. Shima, S. Onoe, M. Hanada, T. Nagai, S Nakajima. S. Okada: "Botryoid Wilms tumor : case report and review of literature"Pediatric Nephrology. 14. 59-61 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] S. Nakajima, et al: "Effect of cyclic adenosine 3',5'-monophosphate and protein kinase A on ligand-dependent transactivation via the vitamin D receptor"Molecular and Cellular Endocrinology. 159. 45-51 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] S. Matsumoto, S. Nakajima. et al: "Interferon treatment on glomerulonephritis associated with hepatitis C virus"Pediatric Nephrology. 15. 271-273 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] H. Hirai, S. Nakajima. et al: "A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia"Journal of Human Genetics. 46. 41-44 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] T. Kubota, H. Hirai, N. Shimizu, A. Sawada, H. Kondou, S. Nakajima, et al: "Development of hyperthyroidism in a patient with idiopathic nephrotic syndrome"Pediatric Nephrology. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] H.Hirai, S.Nakajima, et al.: "A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia"Journal of Human Genetics. 46. 41-44 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] T.Kubota, H.Hirai, N.Shimizu, A.Sawada, H.Kondou, S.Nakajima, et al.: "Development of hyperthyroidism in a patient with idiopathic nephrotic syndrome"Pediatric Nephrology. (in press).

    • Related Report
      2001 Annual Research Report
  • [Publications] M.Akagi,K.Inui,S.Nakajima, et al.: "Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome."Journal of Human Genetics. 45. 60-62 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] S.Nakajima, et al.: "Effect of cyclic adenosine 3',5'-monophosphate and protein kinase A on ligand-dependent transactivation via the vitamin D receptor."Molecular and Cellular Endocrinology. 159. 45-51 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] S.Matsumoto,S.Nakajima, et al.: "Interferon treatment glomerulonephritis associated with hepatitis C virus."Pediatric Nephrology. 15. 271-273 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] H.Hirai,S.Nakajima, et al.: "A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia."Journal of Human Genetics. 46. 41-44 (2000)

    • Related Report
      2000 Annual Research Report

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Published: 2001-04-01   Modified: 2016-04-21  

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