Literature DB >> 11983294

14-3-3 in the cerebrospinal fluid of patients with variant and sporadic Creutzfeldt-Jakob disease measured using capture assay able to detect low levels of 14-3-3 protein.

Alison J E Green1, Sanja Ramljak, Werner E G Müller, Richard S G Knight, Heinz C Schröder.   

Abstract

A protein capture assay was used to measure 14-3-3 (-isoform) in the cerebrospinal fluid (CSF) of patients with either variant or sporadic Creutzfeldt-Jakob disease (CJD). The results were compared with those obtained using Western blotting. Elevated levels of 14-3-3 were found in 58% of variant CJD (vCJD) patients and 82% of sporadic CJD (spCJD) patients using the protein capture assay. Using a Western blotting technique, the presence of CSF 14-3-3 was detected in 58% of vCJD patients and in 89% of spCJD patients. When the results from the protein capture assay and the Western blot were combined, 14-3-3 was detected in 77% of vCJD patients and in 91% of spCJD patients. These results suggest that although analysis of CSF 14-3-3 is not as useful in vCJD as it is in the sporadic form of the disease, a combination of these two techniques results in increased sensitivity of 14-3-3 for the diagnosis of vCJD.

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Year:  2002        PMID: 11983294     DOI: 10.1016/s0304-3940(02)00172-6

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  7 in total

1.  Characteristics of Korean patients with suspected Creutzfeldt-Jakob disease with 14-3-3 protein in cerebrospinal fluid: Preliminary study of the Korean Creutzfeldt-Jakob disease active surveillance program.

Authors:  Jae-Sung Lim; Hyung-Min Kwon; Jae-Won Jang; Young-Ran Ju; SuYeon Kim; Young Ho Park; So Young Park; SangYun Kim
Journal:  Prion       Date:  2015       Impact factor: 3.931

2.  CSF Tau proteins reduce misdiagnosis of sporadic Creutzfeldt-Jakob disease suspected cases with inconclusive 14-3-3 result.

Authors:  M J Leitão; I Baldeiras; M R Almeida; M H Ribeiro; A C Santos; M Ribeiro; J Tomás; S Rocha; I Santana; C R Oliveira
Journal:  J Neurol       Date:  2016-06-29       Impact factor: 4.849

3.  Tau and 14-3-3 of genetic and sporadic Creutzfeldt-Jakob disease patients in Israel.

Authors:  Zeev Meiner; Esther Kahana; Fanny Baitcher; Amos D Korczyn; Joab Chapman; Oren S Cohen; Ron Milo; Judith Aharon-Perez; Oded Abramsky; Ruth Gabizon; Hanna Rosenmann
Journal:  J Neurol       Date:  2010-09-09       Impact factor: 4.849

4.  Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients.

Authors:  Inês Esteves Baldeiras; Maria Helena Ribeiro; Paula Pacheco; Alvaro Machado; Isabel Santana; Luís Cunha; Catarina Resende Oliveira
Journal:  J Neurol       Date:  2009-05-06       Impact factor: 4.849

5.  Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD.

Authors:  Natividad Cuadrado-Corrales; Adolfo Jiménez-Huete; Carmen Albo; Rafael Hortigüela; Luz Vega; Laura Cerrato; Maríajosé Sierra-Moros; Alberto Rábano; Jesús de Pedro-Cuesta; Miguel Calero
Journal:  BMC Neurol       Date:  2006-07-26       Impact factor: 2.474

Review 6.  Role of Biomarkers for the Diagnosis of Prion Diseases: A Narrative Review.

Authors:  Miren Altuna; Iñigo Ruiz; María Victoria Zelaya; Maite Mendioroz
Journal:  Medicina (Kaunas)       Date:  2022-03-25       Impact factor: 2.948

Review 7.  Challenges and Advances in Antemortem Diagnosis of Human Transmissible Spongiform Encephalopathies.

Authors:  Lucas M Ascari; Stephanie C Rocha; Priscila B Gonçalves; Tuane C R G Vieira; Yraima Cordeiro
Journal:  Front Bioeng Biotechnol       Date:  2020-10-20
  7 in total

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