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      KCI등재 SCIE SCOPUS

      Real-Time Quaking-Induced Conversion Analysis for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Korea

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      https://www.riss.kr/link?id=A105872293

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      다국어 초록 (Multilingual Abstract)

      Background and Purpose Te level of 14-3-3 protein in the cerebrospinal fuid (CSF) is increased in Creutzfeldt-Jakob disease (CJD) patients, which has led to it being used as a clinical biomarker for the ante-mortem diagnosis of human prion diseases. However, the specifcity of the 14-3-3 protein is less reliable for CJD diagnosis. Newly developed assays including real-time quaking-induced conversion (RT-QuIC) have made it possible to detect the PrPSc-like abnormal prion isoform with a high sensitivity in animal and human specimens that might contain a minute amount of PrPScdue to in vitro prion replication.
      MethodszzTis study applied a highly sensitive RT-QuIC assay using recombinant human PrP to detect PrPScin the CSF of 81 patients with sporadic CJD (sCJD) in Korea.
      ResultszzRT-QuIC analysis of the CSF samples based on the expression levels of 14-3-3 and total tau proteins revealed positivity in 62 of 81 sCJD patients (sensitivity of 76.5%) but no positive results in the 100 non-CJD patients.
      Conclusions Te sensitivity of the RT-QuIC in this study was similar to that in some previous reports, and the specifcity of RT-QuIC was higher than that of 14-3-3 in CSF, suggesting that RT-QuIC analysis can complement the weakness of the specifcity of 14-3-3 for the diagnosis of sCJD. Tese results indicate that RT-QuIC might be very useful for the rapid and specifc diagnosis of sCJD and provide a practical novel method for the ante-mortem diagnosis of human prion diseases.
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      Background and Purpose Te level of 14-3-3 protein in the cerebrospinal fuid (CSF) is increased in Creutzfeldt-Jakob disease (CJD) patients, which has led to it being used as a clinical biomarker for the ante-mortem diagnosis of human prion diseases. H...

      Background and Purpose Te level of 14-3-3 protein in the cerebrospinal fuid (CSF) is increased in Creutzfeldt-Jakob disease (CJD) patients, which has led to it being used as a clinical biomarker for the ante-mortem diagnosis of human prion diseases. However, the specifcity of the 14-3-3 protein is less reliable for CJD diagnosis. Newly developed assays including real-time quaking-induced conversion (RT-QuIC) have made it possible to detect the PrPSc-like abnormal prion isoform with a high sensitivity in animal and human specimens that might contain a minute amount of PrPScdue to in vitro prion replication.
      MethodszzTis study applied a highly sensitive RT-QuIC assay using recombinant human PrP to detect PrPScin the CSF of 81 patients with sporadic CJD (sCJD) in Korea.
      ResultszzRT-QuIC analysis of the CSF samples based on the expression levels of 14-3-3 and total tau proteins revealed positivity in 62 of 81 sCJD patients (sensitivity of 76.5%) but no positive results in the 100 non-CJD patients.
      Conclusions Te sensitivity of the RT-QuIC in this study was similar to that in some previous reports, and the specifcity of RT-QuIC was higher than that of 14-3-3 in CSF, suggesting that RT-QuIC analysis can complement the weakness of the specifcity of 14-3-3 for the diagnosis of sCJD. Tese results indicate that RT-QuIC might be very useful for the rapid and specifc diagnosis of sCJD and provide a practical novel method for the ante-mortem diagnosis of human prion diseases.

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      참고문헌 (Reference)

      1 Atarashi R, "Ultrasensitive human prion detection in cerebrospinal fluid by realtime quaking-induced conversion" 17 : 175-178, 2011

      2 Peden AH, "Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion" 93 (93): 438-449, 2012

      3 Atarashi R, "Real-time quaking-induced conversion: a highly sensitive assay for prion detection" 5 : 150-153, 2011

      4 Orrú CD, "Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid" 6 (6): e02451-02414, 2015

      5 Tschampa HJ, "Radiological assessment of Creutzfeldt-Jakob disease" 17 : 1200-1211, 2007

      6 LeVine H 3rd, "Quantification of beta-sheet amyloid fibril structures with thioflavin T" 309 : 274-284, 1999

      7 Aguzzi A, "Progress and problems in the biology, diagnostics, and therapeutics of prion diseases" 114 : 153-160, 2004

      8 Jeong BH, "Polymorphisms of the prion protein gene (PRNP) in a Korean population" 49 : 319-324, 2004

      9 Orrù CD, "New generation QuIC assays for prion seeding activity" 6 : 147-152, 2012

      10 Shimada T, "Neuroprotective function of 14-3-3 proteins in neurodegeneration" 2013 : 564534-, 2013

      1 Atarashi R, "Ultrasensitive human prion detection in cerebrospinal fluid by realtime quaking-induced conversion" 17 : 175-178, 2011

      2 Peden AH, "Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion" 93 (93): 438-449, 2012

      3 Atarashi R, "Real-time quaking-induced conversion: a highly sensitive assay for prion detection" 5 : 150-153, 2011

      4 Orrú CD, "Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid" 6 (6): e02451-02414, 2015

      5 Tschampa HJ, "Radiological assessment of Creutzfeldt-Jakob disease" 17 : 1200-1211, 2007

      6 LeVine H 3rd, "Quantification of beta-sheet amyloid fibril structures with thioflavin T" 309 : 274-284, 1999

      7 Aguzzi A, "Progress and problems in the biology, diagnostics, and therapeutics of prion diseases" 114 : 153-160, 2004

      8 Jeong BH, "Polymorphisms of the prion protein gene (PRNP) in a Korean population" 49 : 319-324, 2004

      9 Orrù CD, "New generation QuIC assays for prion seeding activity" 6 : 147-152, 2012

      10 Shimada T, "Neuroprotective function of 14-3-3 proteins in neurodegeneration" 2013 : 564534-, 2013

      11 양태일, "Familial Creutzfeldt-Jakob Disease with V180I Mutation" 대한의학회 25 (25): 1097-1100, 2010

      12 Sano K, "Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay" 8 : e54915-, 2013

      13 Skillbäck T, "Diagnostic performance of cerebrospinal fluid total tau and phosphorylated tau in Creutzfeldt-Jakob disease: results from the Swedish Mortality Registry" 71 : 476-483, 2014

      14 Kübler E, "Diagnosis of prion diseases" 66 : 267-279, 2003

      15 Cramm M, "Characteristic CSF prion seeding efficiency in humans with prion diseases" 51 : 396-405, 2015

      16 Stoeck K, "Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years" 135 (135): 3051-3061, 2012

      17 Orrú CD, "A test for Creutzfeldt-Jakob disease using nasal brushings" 371 : 519-529, 2014

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2012-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2011-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2008-01-01 평가 SCIE 등재 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 2.07 0.25 1.55
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.25 1.08 0.497 0.02
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