Literature DB >> 29097599

Brains with sporadic Creutzfeldt-Jakob disease and copathology showed a prolonged end-stage of disease.

Aitzol Miguelez-Rodriguez1, Jorge Santos-Juanes2, Ikerne Vicente-Etxenausia3, Katty Perez de Heredia-Goñi3, Beatriz Garcia4, Luis M Quiros4,5, Laura Lorente-Gea6, Isabel Guerra-Merino1,3,6, Jose J Aguirre6, Ivan Fernandez-Vega2,3,4,6.   

Abstract

AIMS: To investigate the expression of major proteins related to primary neurodegenerative diseases and their prognostic significance in brains with Creutzfeldt-Jakob disease (CJD).
MATERIALS AND METHODS: Thirty consecutive cases of confirmed CJD during the period 2010-2015 at Basque Brain bank were retrospectively reviewed. Moreover, major neurodegenerative-associated proteins (phosphorylated Tau, 4R tau, 3R tau, alpha-synuclein, TDP43, amyloid beta) were tested. Clinical data were reviewed. Cases were divided according to the presence or absence of copathology. Survival curves were also determined.
RESULTS: Copathology was significantly associated with survival in brains with CJD (4.2±1.2 vs 9.2±1.9; P=0.019) and in brains with MM1/MV1 CJD (2.1±1.0 vs 6.7±2.8; P=0.012). Besides, the presence of more than one major neurodegenerative-associated protein was significantly associated with survival (4.2±1.2 vs 10.7±2.6; P=0.017). Thus, univariate analyses further pointed out variables significantly associated with better survival: copathology in CJD (HR=0.430; P=0.033); more than one neurodegenerative-associated protein in CJD (HR=0.369; P=0.036) and copathology in MM1/MV1 CJD (HR=0.525; P=0.032).
CONCLUSION: The existence of copathology significantly prolongs survival in patients with rapidly progressive dementia due to CJD. The study of major neurodegenerative-associated proteins in brains with CJD could allow us to further understand the molecular mechanisms behind prion diseases. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  brain; immunohistochemistry; neurodegeneration; neuropathology; proteins

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Year:  2017        PMID: 29097599     DOI: 10.1136/jclinpath-2017-204794

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  2 in total

1.  Brain Donation Decisions as Disease Specific Behaviors: An Elucidation of the Donation Process in the Context of Essential Tremor.

Authors:  Daniella Iglesias-Hernandez; Diane Berry; Nora Hernandez; Elan D Louis
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2022-08-23

2.  PART and ARTAG tauopathies at a relatively young age as a concomitant finding in sporadic Creutzfeldt-Jakob disease.

Authors:  Kateřina Menšíková; Radoslav Matěj; Eva Parobková; Magdalena Smětáková; Petr Kaňovský
Journal:  Prion       Date:  2021-12       Impact factor: 3.931

  2 in total

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