|
|
||||||||
From the Department of Neurology (Drs. Lemstra, van Meegen, Vreyling, Meijerink, Bulk, Baas, and van Gool), Academic Medical Center, University of Amsterdam; and the Department of Pathology (Dr. Jansen), University Medical Center Utrecht, the Netherlands.
Address correspondence and reprint requests to Dr. A.W. Lemstra, Department of Neurology, Academic Medical Center Amsterdam, the Netherlands; e-mail: a.w.lemstra{at}amc.uva.nl
OBJECTIVE: To study the sensitivity and specificity of 14-3-3 testing in a prospective series of patients suspected of having Creutzfeldt-Jakob disease (CJD).
BACKGROUND: The 14-3-3 protein immunoassay on CSF has favorable test characteristics as a premortem diagnostic tool in CJD. However, the 14-3-3 protein is a normal cellular protein expressed in various tissues, and its presence in CSF reflects extensive destruction of brain tissue as in CJD, but also in ischemic stroke and meningoencephalitis.
METHODS: 14-3-3 was tested in the CSF of a prospective series of 110 consecutive patients suspected of having CJD.
RESULTS: The sensitivity was 97% and the specificity was 87% in this series. False-positive results were mainly caused by stroke and meningoencephalitis.
CONCLUSION: The 14-3-3 protein is a highly sensitive and specific marker for CJD when used in the appropriate clinical context.
This article has been cited by other articles:
![]() |
P. Brown Transmissible spongiform encephalopathy in the 21st century: Neuroscience for the clinical neurologist Neurology, February 26, 2008; 70(9): 713 - 722. [Full Text] [PDF] |
||||
![]() |
Y. Shiga, K. Miyazawa, S. Sato, R. Fukushima, S. Shibuya, Y. Sato, H. Konno, K. Doh-ura, S. Mugikura, H. Tamura, et al. Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease Neurology, August 10, 2004; 63(3): 443 - 449. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Huang, S. K. Marie, J. A. Livramento, R. Chammas, and R. Nitrini 14-3-3 protein in the CSF of patients with rapidly progressive dementia Neurology, August 12, 2003; 61(3): 354 - 357. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. F. Al Otaibi, B. A. Minassian, C. A. Ackerley, W. J. Logan, and S. Weiss Unusual Presentation of Lafora's Disease J Child Neurol, July 1, 2003; 18(7): 499 - 501. [Abstract] [PDF] |
||||
![]() |
M. D. Geschwind, J. Martindale, D. Miller, S. J. DeArmond, J. Uyehara-Lock, D. Gaskin, J. H. Kramer, N. M. Barbaro, and B. L. Miller Challenging the Clinical Utility of the 14-3-3 Protein for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease Arch Neurol, June 1, 2003; 60(6): 813 - 816. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Rentz Creutzfeldt-Jakob disease: Two case studies American Journal of Alzheimer's Disease and Other Dementias, May 1, 2003; 18(3): 171 - 180. [Abstract] [PDF] |
||||
![]() |
K. Peoc'h, P. Beaudry, N. Laupretre, J.-L. Laplanche, P. R. Burkhard, J.-C. Sanchez, T. Landis, and D. F. Hochstrasser CSF detection of the 14-3-3 protein in unselected patients with dementia Neurology, February 12, 2002; 58(3): 509 - 510. [Full Text] [PDF] |
||||
![]() |
P. R. Burkhard, J.-C. Sanchez PhD, T. Landis, and D. F. Hochstrasser CSF detection of the 14-3-3 protein in unselected patients with dementia Neurology, June 12, 2001; 56(11): 1528 - 1533. [Abstract] [Full Text] [PDF] |
||||
![]() |
A J E Green, E J Thompson, G E Stewart, M Zeidler, J M McKenzie, M-A MacLeod, J W Ironside, R G Will, and R S G Knight Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease J. Neurol. Neurosurg. Psychiatry, June 1, 2001; 70(6): 744 - 748. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |