Literature DB >> 26014384

CSF tau correlates with CJD disease severity and cognitive decline.

O S Cohen1,2, J Chapman1,2, A D Korczyn2, N Warman-Alaluf1, Z Nitsan3, S Appel3, E Kahana3, H Rosenmann4.   

Abstract

BACKGROUND: Creutzfeldt-Jakob disease (CJD) is the most common prion disease in humans. The clinical diagnosis of CJD is supported by a combination of electroencephalogram, MRI, and the presence in the CSF of biomarkers. CSF tau is a marker for neuronal damage and tangle pathology, and is correlated with cognitive status in Alzheimer's disease (AD).
OBJECTIVES: The aim of this study was to test whether tau levels in the CSF also correlate with the degree of the neurological deficit and cognitive decline in patients with CJD as reflected by various clinical scales that assess disease severity and cognitive performance.
METHODS: Consecutive patients with familial CJD (fCJD) were examined by a neurologist who performed several tests including minimental status examination (MMSE), frontal assessment battery (FAB), NIH stroke scale (NIHSS), CJD neurological scale (CJD-NS), and the expanded disability status scale (EDSS). CSF tau was tested as part of the workout, and the correlation was tested using Pearson correlation.
RESULTS: Fifty-two patients with fCJD were recruited to the study (35 males, mean age 59.4 ± 5.7, range 48-75 years). A significant negative correlation was found between CSF tau levels and the cognitive performance of the patients as reflected by their MMSE and FAB scores. In addition, a significant positive correlation was found between tau levels and the clinical disease severity scales of CJD-NS, NIHSS, and EDSS.
CONCLUSION: The correlation between tau levels and the disease severity and degree of cognitive decline in patients with fCJD suggests that tau can be a biomarker reflecting the extent of neuronal damage.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Creutzfeldt-Jakob disease; E200K mutation; Tau protein; cognitive decline

Year:  2015        PMID: 26014384     DOI: 10.1111/ane.12441

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  12 in total

1.  Disease duration in E200K familial Creutzfeldt-Jakob disease is correlated with clinical, radiological, and laboratory variables.

Authors:  Oren S Cohen; Joab Chapman; Amos D Korczyn; Zeev Nitsan; Shmuel Appel; Esther Kahana; Hanna Rosenmann; Chen Hoffmann
Journal:  J Neural Transm (Vienna)       Date:  2018-11-29       Impact factor: 3.575

2.  Cerebrospinal fluid β-amyloid42 and neurofilament light relate to white matter hyperintensities.

Authors:  Katie E Osborn; Dandan Liu; Lauren R Samuels; Elizabeth E Moore; Francis E Cambronero; Lealani Mae Y Acosta; Susan P Bell; Michelle A Babicz; Elizabeth A Gordon; Kimberly R Pechman; L Taylor Davis; Katherine A Gifford; Timothy J Hohman; Kaj Blennow; Henrik Zetterberg; Angela L Jefferson
Journal:  Neurobiol Aging       Date:  2018-04-03       Impact factor: 4.673

3.  Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report.

Authors:  Adrianna E Carrasco; Brian S Appleby; Ignazio Cali; Hamid R Okhravi
Journal:  Front Neurol       Date:  2022-05-09       Impact factor: 4.086

4.  Cerebrospinal Fluid Biomarkers in the Diagnosis of Creutzfeldt-Jakob Disease in Slovak Patients: over 10-Year Period Review.

Authors:  Silvia Koscova; Dana Zakova Slivarichova; Ivana Tomeckova; Katarina Melicherova; Martin Stelzer; Alzbeta Janakova; Dana Kosorinova; Girma Belay; Eva Mitrova
Journal:  Mol Neurobiol       Date:  2016-09-24       Impact factor: 5.590

5.  NIA-AA staging of preclinical Alzheimer disease: discordance and concordance of CSF and imaging biomarkers.

Authors:  Stephanie J B Vos; Brian A Gordon; Yi Su; Pieter Jelle Visser; David M Holtzman; John C Morris; Anne M Fagan; Tammie L S Benzinger
Journal:  Neurobiol Aging       Date:  2016-04-04       Impact factor: 4.673

Review 6.  Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.

Authors:  Peter Hermann; Brian Appleby; Jean-Philippe Brandel; Byron Caughey; Steven Collins; Michael D Geschwind; Alison Green; Stephane Haïk; Gabor G Kovacs; Anna Ladogana; Franc Llorens; Simon Mead; Noriyuki Nishida; Suvankar Pal; Piero Parchi; Maurizio Pocchiari; Katsuya Satoh; Gianluigi Zanusso; Inga Zerr
Journal:  Lancet Neurol       Date:  2021-03       Impact factor: 44.182

7.  Selective vulnerability to atrophy in sporadic Creutzfeldt-Jakob disease.

Authors:  Kyan Younes; Julio C Rojas; Amy Wolf; Goh M Sheng-Yang; Matteo Paoletti; Gianina Toller; Eduardo Caverzasi; Maria Luisa Mandelli; Ignacio Illán-Gala; Joel H Kramer; Yann Cobigo; Bruce L Miller; Howard J Rosen; Michael D Geschwind
Journal:  Ann Clin Transl Neurol       Date:  2021-05-05       Impact factor: 4.511

8.  Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation.

Authors:  Nathalie Daude; Chae Kim; Sang-Gyun Kang; Ghazaleh Eskandari-Sedighi; Tracy Haldiman; Jing Yang; Shelaine C Fleck; Erik Gomez-Cardona; Zhuang Zhuang Han; Sergi Borrego-Ecija; Serene Wohlgemuth; Olivier Julien; Holger Wille; Laura Molina-Porcel; Ellen Gelpi; Jiri G Safar; David Westaway
Journal:  Acta Neuropathol       Date:  2020-03-26       Impact factor: 17.088

9.  Neurofilament light chain and tau concentrations are markedly increased in the serum of patients with sporadic Creutzfeldt-Jakob disease, and tau correlates with rate of disease progression.

Authors:  Andrew Geoffrey Bourne Thompson; Connie Luk; Amanda J Heslegrave; Henrik Zetterberg; Simon H Mead; John Collinge; Graham S Jackson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2018-02-27       Impact factor: 10.154

Review 10.  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
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