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Amplification techniques and diagnosis of prion diseases

Authors :
Stéphane Haïk
Jean-Louis Laplanche
Jean-Philippe Brandel
Etienne Levavasseur
Audrey Culeux
P. Lamy
Arlette Welaratne
Katarina Grznarova
A. Denouel
Nicolas Privat
Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM)
Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Source :
Revue Neurologique, Revue Neurologique, Elsevier Masson, 2019, 175, pp.458-463. ⟨10.1016/j.neurol.2019.06.002⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

Protein misfolding cyclic amplification assay (PMCA) and real-time quaking-induced conversion (RT-QuIC) are two amplification techniques based on the ability of PrPsc to induce a conformational change in PrP allowing the detection of minute amounts of PrPsc in body fluids or tissues. PMCA and RT-QuIC have different ability to amplify PrPsc from sporadic, variant and genetic forms of Creutzfeldt-Jakob disease (CJD). PMCA readily amplifies PrPsc from variant CJD (vCJD) tissue while RT-QuIC easily amplifies PrPsc from sporadic CJD (sCJD) patient tissues. In terms of diagnosis, this implies the possibility of distinguishing vCJD from sCJD and explains the wider use of RT-QuIC given the respective frequencies of vCJD and sCJD. The sensitivity values of RT-QuIC for the diagnosis of sCJD are comparable or higher than those of the other tests (EEG, MRI, detection of 14-3-3 or tau proteins in cerebrospinal fluid) but with a specificity close to 100%. These new diagnostic methods could also be useful for the diagnosis of other neurodegenerative diseases.

Details

Language :
English
ISSN :
00353787
Database :
OpenAIRE
Journal :
Revue Neurologique, Revue Neurologique, Elsevier Masson, 2019, 175, pp.458-463. ⟨10.1016/j.neurol.2019.06.002⟩
Accession number :
edsair.doi.dedup.....fe20badbdfbeb35921507d656b90e0d1
Full Text :
https://doi.org/10.1016/j.neurol.2019.06.002⟩