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A study for establishment of diagnostic markers in sudden infant death syndrome by imaging mass spectrometry.

Research Project

Project/Area Number 22790603
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Legal medicine
Research InstitutionOsaka Medical College

Principal Investigator

SATO Takako  大阪医科大学, 医学部, 助教 (10530420)

Project Period (FY) 2010 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords法医病理学 / 乳幼児突然死症候群 / 質量顕微鏡 / ミエリン塩基性蛋白
Research Abstract

Sudden infant death syndrome(SIDS) is one of the major causes of infant mortality. However, the causes of SIDS are still unknown. It is pointed out that developmental delays in the central cardiovascular and respiratory regulation may be involved. Our research intended to examine whether myelin structural proteins, such as myelin basic protein(MBP), are useful as diagnostic markers of SIDS by direct analysis of brain tissue using imaging mass spectrometry. Paraffin-embedded sections seemed to be ideal because the cases have been accumulated, but they were found to be unsuitable for the analysis. Though frozen sections are suitable, the number of cases is insufficient. It is necessary to accumulate the number of samples for further study.

Report

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

    (7 results)

All 2012 2011 2010

All Journal Article (7 results) (of which Peer Reviewed: 7 results)

  • [Journal Article] Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect2012

    • Author(s)
      Sato T, Abe S, Tsuboi K, Iwata M, Tamura A, Tsuchihashi H, Nishio H, Suzuki K
    • Journal Title

      Leg Med

      Volume: 14(3) Pages: 157-9

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect2012

    • Author(s)
      Sato T, et.al
    • Journal Title

      Leg Med (Tokyo)

      Volume: 14(3) Issue: 3 Pages: 157-9

    • DOI

      10.1016/j.legalmed.2012.01.010

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution : a case report2011

    • Author(s)
      Sato T, Nishio H, Suzuki K
    • Journal Title

      Leg Med

      Volume: 13(6) Pages: 298-30

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Recently abused β-keto derivatives of 3, 4-methylenedioxyphenylalkylamines : a review of their metabolisms and toxicological analysis2011

    • Author(s)
      Zaitsu K, Katagi M, Tatsuno M, Sato T, Tsuchihashi H, Suzuki K
    • Journal Title

      FORENSIC TOXICOLOGY

      Volume: Volume 29 Pages: 73-84

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution : a case report2011

    • Author(s)
      Sato T, et.al
    • Journal Title

      Leg Med (Tokyo)

      Volume: 13(6) Issue: 6 Pages: 298-300

    • DOI

      10.1016/j.legalmed.2011.08.004

    • Related Report
      2011 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome2010

    • Author(s)
      Takahashi M, Sato T, Nishiguchi M, Suzuki K, Nishio H
    • Journal Title

      Leg Med

      Volume: 12(6) Pages: 305-7

    • NAID

      10029883452

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Postmortem molecular screening for mutations in ryanodine receptor type 1(RYR1) gene in psychiatric patients suspected of having died of neuroleptic malignant syndrome2010

    • Author(s)
      Sato T, Nishio H, Iwata M, Kentotsuboi, Tamura A, Miyazaki T, Suzuki K
    • Journal Title

      Forensic Sci Int

      Volume: 194(1-3) Pages: 77-9

    • Related Report
      2011 Final Research Report
    • Peer Reviewed

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Published: 2010-11-30   Modified: 2016-04-21  

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