Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2013 May-Jun;7(3):229-34.
doi: 10.4161/pri.23904. Epub 2013 Feb 13.

CSF prion protein concentration and cognition in patients with Alzheimer disease

Affiliations
Observational Study

CSF prion protein concentration and cognition in patients with Alzheimer disease

Christian Schmidt et al. Prion. 2013 May-Jun.

Abstract

Background/objective: PrP (c) has been suggested to play a role in AD pathophysiology. CSF concentrations of PrP (c) have been shown to be reduced in AD compared with healthy controls. Furthermore, serum levels of PrP (c) have recently been reported to be associated with the cognitive status of healthy elderly subjects. Therefore, we hypothesized that CSF levels of PrP (c) could be associated with cognitive function of AD patients at the time of diagnosis.

Methods: AD patients (n = 114) included into an observational study underwent CERAD testing and lumbar puncture at time of diagnosis / study inclusion. CSF PrP (c) was determined. Generalized linear models were fitted to assess the associations of PrP (c) plus a variety of possible confounding factors and CERAD subscale measures.

Results: No association of CSF PrP (c) and cognitive status could be established, while other factors (i.e., use of antipsychotic drugs, use of anti-dementia drugs, female sex, pre-progression time) were related to worse cognitive function in some domains.

Conclusion: CSF PrP (c) appears not to be a useful biochemical surrogate of cognitive status in AD at the time of diagnosis. Follow-up analyses will examine possible associations with the speed of cognitive decline.

Keywords: Alzheimer; CSF; biomarker; cognition; prion protein.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Thies W, Bleiler L. 2011 Alzheimer disease facts and figures. Alzheimer & Dementia. 2011;7:208–44. doi: 10.1016/j.jalz.2011.02.004. - DOI - PubMed
    1. Parkin ET, Watt NT, Hussain I, Eckman EA, Eckman CB, Manson JC, et al. Cellular prion protein regulates beta-secretase cleavage of the Alzheimer’s amyloid precursor protein. Proc Natl Acad Sci U S A. 2007;104:11062–7. doi: 10.1073/pnas.0609621104. - DOI - PMC - PubMed
    1. Um JW, Strittmatter SM. Amyloid-ß induced signaling by cellular prion protein and Fyn kinase in Alzheimer disease. Prion. 2012;6 - PMC - PubMed
    1. Kudo W, Lee H-P, Zou W-Q, Wang X, Perry G, Zhu X, et al. Cellular prion protein is essential for oligomeric amyloid-β-induced neuronal cell death. Hum Mol Genet. 2012;21:1138–44. doi: 10.1093/hmg/ddr542. - DOI - PMC - PubMed
    1. Kessels HW, Nguyen LN, Nabavi S, Malinow R. The prion protein as a receptor for amyloid-beta. Nature. 2010;466:E3–4, discussion E4-5. doi: 10.1038/nature09217. - DOI - PMC - PubMed

Publication types