alexa Subtype Specific CSF Biomarkers in Sporadic Creutzfeldt-Jakob Disease
ISSN: 2161-0460

Journal of Alzheimers Disease & Parkinsonism
Open Access

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Subtype Specific CSF Biomarkers in Sporadic Creutzfeldt-Jakob Disease

Saima Zafar*, Neelam Younas and Inga Zerr

Clinical Dementia Center and DZNE, University Medical Center Gottingen (UMG), Göttingen, Germany

*Corresponding Author:
Saima Zafar
Department of Neurology, Clinical Dementia Center and DZNE
University Medical Centre Gottingen, Gottingen, Germany
Tel: 00495513914962
E-mail: [email protected]

Received date: May 02, 2017; Accepted date: May 31, 2017; Published date: June 07, 2017

Citation: Zafar S, Younas N, Zerr I (2017) Subtype Specific CSF Biomarkers in Sporadic Creutzfeldt-Jakob Disease. J Alzheimers Dis Parkinsonism 7:332. doi:10.4172/2161-0460.1000332

Copyright: © 2017 Zafar S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare but fatal type of spongiform encephalopathy with unidentified origin. The conjoining methionine-valine polymorphism of PRNP gene at codon 129 and two types of prion protein (PrPsc types 1 and 2) described the six different molecular subtypes (MM1, MM2, MV1, MV2, VV1 and VV2) of sCJD. Presumptive subtype specific diagnosis showed differential clinical manifestations and levels of CSF 14-3-3 protein. Even with the above mentioned differential diagnostic guidelines, pre-mortem subtype specific diagnosis of sCJD can be unreliable with high rates of misdiagnosis. The need for more reliable biomarkers for improving the diagnosis as well as understanding the pathogenesis of this mysterious ailment is amplified. This review compiles the levels of CSF proteins, i.e., PrPC, PrPSC 14-3-3, tau, phosphorylated tau, S100B, neuron-specific enolase (NSE) alpha-synuclein and beta-amyloid to differential diagnosis subtype specific sCJD cases. The detection of pre-mortem distinction targets might be useful diagnostic tool for sCJD in subtype specific manner and might lead towards differential treatment approaches.

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