Literature DB >> 22843257

A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease.

Clive Hamlin1, Gianfranco Puoti, Sally Berri, Elliott Sting, Carrie Harris, Mark Cohen, Charles Spear, Alberto Bizzi, Sara M Debanne, Douglas Y Rowland.   

Abstract

OBJECTIVE: To compare the respective efficiency of CSF tau (quantitative) and CSF 14-3-3 protein (qualitative) in the diagnosis of prion disease.
METHODS: We made measurements on 420 live subjects, who subsequently underwent a postmortem neuropathology examination, including protein chemistry, immunohistochemistry, and histology. We performed tau by ELISA. We detected 14-3-3 protein by Western blot. Both assays were optimized for maximum efficiency (accuracy).
RESULTS: We found tau and 14-3-3 proteins to be closely correlated, but tau had a significantly better ability to predict disease status than 14-3-3 protein. Also, tau distinguished disease status at least as well as when both assays' results are combined in a variety of ways. Importantly, the area under the receiver operating characteristic curve for tau (0.82) was significantly larger than that for 14-3-3 protein (0.68) (p < 0.001). Diagnostic test statistics are provided for the study subjects with 58.3% prevalence, and for a more typical, nonselected, 7.5% prevalence as received by our center.
CONCLUSION: In this study, tau is superior to 14-3-3 protein as a marker in the diagnosis of Creutzfeldt-Jakob disease, and is as efficient singly compared to a variety of combinations with 14-3-3 protein. This is the first study of this magnitude to examine prion disease diagnostic tests in a carefully characterized patient population with detailed statistical evaluation.

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Year:  2012        PMID: 22843257      PMCID: PMC4098812          DOI: 10.1212/WNL.0b013e318263565f

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  26 in total

1.  14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes.

Authors:  K Gmitterová; U Heinemann; M Bodemer; A Krasnianski; B Meissner; H A Kretzschmar; I Zerr
Journal:  Neurobiol Aging       Date:  2008-03-06       Impact factor: 4.673

2.  The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies.

Authors:  G Hsich; K Kenney; C J Gibbs; K H Lee; M G Harrington
Journal:  N Engl J Med       Date:  1996-09-26       Impact factor: 91.245

3.  Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob disease.

Authors:  S Kropp; I Zerr; W J Schulz-Schaeffer; C Riedemann; M Bodemer; C Laske; H A Kretzschmar; S Poser
Journal:  Neurosci Lett       Date:  1999-02-12       Impact factor: 3.046

4.  CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.

Authors:  P Sanchez-Juan; A Green; A Ladogana; N Cuadrado-Corrales; R Sáanchez-Valle; E Mitrováa; K Stoeck; T Sklaviadis; J Kulczycki; K Hess; M Bodemer; D Slivarichová; A Saiz; M Calero; L Ingrosso; R Knight; A C J W Janssens; C M van Duijn; I Zerr
Journal:  Neurology       Date:  2006-08-22       Impact factor: 9.910

Review 5.  Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease.

Authors:  B Van Everbroeck; J Boons; P Cras
Journal:  Clin Neurol Neurosurg       Date:  2005-01-12       Impact factor: 1.876

6.  14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

Authors:  P Beaudry; P Cohen; J P Brandel; N Delasnerie-Lauprêtre; S Richard; J M Launay; J L Laplanche
Journal:  Dement Geriatr Cogn Disord       Date:  1999 Jan-Feb       Impact factor: 2.959

7.  A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease.

Authors:  B Van Everbroeck; S Quoilin; J Boons; J J Martin; P Cras
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-09       Impact factor: 10.154

8.  Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis.

Authors:  Pascual Sanchez-Juan; Raquel Sánchez-Valle; Alison Green; Anna Ladogana; Natividad Cuadrado-Corrales; Eva Mitrová; Kathrina Stoeck; Theodoros Sklaviadis; Jerzy Kulczycki; Klaus Hess; Anna Krasnianski; Michele Equestre; Danka Slivarichová; Albert Saiz; Miguel Calero; Maurizio Pocchiari; Richard Knight; Cornelia M van Duijn; Inga Zerr
Journal:  J Neurol       Date:  2007-03-25       Impact factor: 4.849

Review 9.  Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.

Authors:  J W Ironside; M W Head
Journal:  Curr Top Microbiol Immunol       Date:  2004       Impact factor: 4.291

10.  Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease.

Authors:  Michael D Geschwind; Jennifer Martindale; Deborah Miller; Stephen J DeArmond; Jane Uyehara-Lock; David Gaskin; Joel H Kramer; Nicholas M Barbaro; Bruce L Miller
Journal:  Arch Neurol       Date:  2003-06
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  47 in total

Review 1.  Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease.

Authors:  Allyson Connor; Han Wang; Brian S Appleby; Daniel D Rhoads
Journal:  J Clin Microbiol       Date:  2019-09-24       Impact factor: 5.948

Review 2.  The use of cerebrospinal fluid and neuropathologic studies in neuropsychiatry practice and research.

Authors:  Kalyani Kansal; David J Irwin
Journal:  Psychiatr Clin North Am       Date:  2015-03-18

3.  Clinical Reasoning: A 64-year-old man with visual distortions.

Authors:  Emer R McGrath; Ayush Batra; Alice D Lam; Joseph F Rizzo; Andrew J Cole
Journal:  Neurology       Date:  2016-11-22       Impact factor: 9.910

Review 4.  Interpretation of cerebrospinal fluid protein tests in the diagnosis of sporadic Creutzfeldt-Jakob disease: an evidence-based approach.

Authors:  Michael B Coulthart; Gerard H Jansen; Neil R Cashman
Journal:  CMAJ       Date:  2014-01-20       Impact factor: 8.262

5.  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

6.  A rare case of rapidly progressive dementia with elevated RT-QuIC and negative 14-3-3 and tau proteins.

Authors:  Bhavesh Trikamji; Clive Hamlin; Kelly J Baldwin
Journal:  Prion       Date:  2016-05-03       Impact factor: 3.931

7.  Diagnostic and prognostic value of human prion detection in cerebrospinal fluid.

Authors:  Aaron Foutz; Brian S Appleby; Clive Hamlin; Xiaoqin Liu; Sheng Yang; Yvonne Cohen; Wei Chen; Janis Blevins; Cameron Fausett; Han Wang; Pierluigi Gambetti; Shulin Zhang; Andrew Hughson; Curtis Tatsuoka; Lawrence B Schonberger; Mark L Cohen; Byron Caughey; Jiri G Safar
Journal:  Ann Neurol       Date:  2017-01       Impact factor: 10.422

Review 8.  Therapies for human prion diseases.

Authors:  Peter K Panegyres; Elizabeth Armari
Journal:  Am J Neurodegener Dis       Date:  2013-09-18

9.  Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC.

Authors:  Samir Abu-Rumeileh; Simone Baiardi; Barbara Polischi; Angela Mammana; Alessia Franceschini; Alison Green; Sabina Capellari; Piero Parchi
Journal:  J Neurol       Date:  2019-09-20       Impact factor: 4.849

10.  A low-molecular-weight ferroxidase is increased in the CSF of sCJD cases: CSF ferroxidase and transferrin as diagnostic biomarkers for sCJD.

Authors:  Swati Haldar; 'alim J Beveridge; Joseph Wong; Ajay Singh; Daniela Galimberti; Barbara Borroni; Xiongwei Zhu; Janis Blevins; Justin Greenlee; George Perry; Chinmay K Mukhopadhyay; Christine Schmotzer; Neena Singh
Journal:  Antioxid Redox Signal       Date:  2013-04-16       Impact factor: 8.401

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