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Published in: BMC Neurology 1/2006

Open Access 01-12-2006 | Research article

Brain-derived proteins in the CSF, do they correlate with brain pathology in CJD?

Authors: Constanze Boesenberg-Grosse, Walter J Schulz-Schaeffer, Monika Bodemer, Barbara Ciesielczyk, Bettina Meissner, Anna Krasnianski, Mario Bartl, Uta Heinemann, Daniela Varges, Sabina Eigenbrod, Hans A Kretzschmar, Alison Green, Inga Zerr

Published in: BMC Neurology | Issue 1/2006

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Abstract

Background

Brain derived proteins such as 14-3-3, neuron-specific enolase (NSE), S 100b, tau, phosphorylated tau and Aβ1–42 were found to be altered in the cerebrospinal fluid (CSF) in Creutzfeldt-Jakob disease (CJD) patients. The pathogenic mechanisms leading to these abnormalities are not known, but a relation to rapid neuronal damage is assumed. No systematic analysis on brain-derived proteins in the CSF and neuropathological lesion profiles has been performed.

Methods

CSF protein levels of brain-derived proteins and the degree of spongiform changes, neuronal loss and gliosis in various brain areas were analyzed in 57 CJD patients.

Results

We observed three different patterns of CSF alteration associated with the degree of cortical and subcortical changes. NSE levels increased with lesion severity of subcortical areas. Tau and 14-3-3 levels increased with minor pathological changes, a negative correlation was observed with severity of cortical lesions. Levels of the physiological form of the prion protein (PrPc) and Aβ1–42 levels correlated negatively with cortical pathology, most clearly with temporal and occipital lesions.

Conclusion

Our results indicate that the alteration of levels of brain-derived proteins in the CSF does not only reflect the degree of neuronal damage, but it is also modified by the localization on the brain pathology. Brain specific lesion patterns have to be considered when analyzing CSF neuronal proteins.
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Literature
1.
go back to reference Hsich G, Kenney K, Gibbs Jr. CJ, Lee KH, Harrington MG: The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongifrom encephalopathies. N Engl J Med. 1996, 335 (13): 924-930. 10.1056/NEJM199609263351303.CrossRefPubMed Hsich G, Kenney K, Gibbs Jr. CJ, Lee KH, Harrington MG: The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongifrom encephalopathies. N Engl J Med. 1996, 335 (13): 924-930. 10.1056/NEJM199609263351303.CrossRefPubMed
2.
go back to reference Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA, Weber T: Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol. 1998, 43 (1): 32-40. 10.1002/ana.410430109.CrossRefPubMed Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA, Weber T: Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol. 1998, 43 (1): 32-40. 10.1002/ana.410430109.CrossRefPubMed
3.
go back to reference Green AJ: Use of 14-3-3 in the diagnosis of Creutzfeldt-Jakob disease. Biochem Soc Symp. 2002, 30: 382-386.CrossRef Green AJ: Use of 14-3-3 in the diagnosis of Creutzfeldt-Jakob disease. Biochem Soc Symp. 2002, 30: 382-386.CrossRef
4.
go back to reference Kohira I, Tsuji T, Ishizu H, Takao Y, Wake A, Abe K, Kuroda S: Elevation of neuron-specific enolase in serum and cerebrospinal fluid of early stage Creutzfeldt-Jakob disease. Acta Neurol Scand. 2000, 102: 385-387. 10.1034/j.1600-0404.2000.102006385.x.CrossRefPubMed Kohira I, Tsuji T, Ishizu H, Takao Y, Wake A, Abe K, Kuroda S: Elevation of neuron-specific enolase in serum and cerebrospinal fluid of early stage Creutzfeldt-Jakob disease. Acta Neurol Scand. 2000, 102: 385-387. 10.1034/j.1600-0404.2000.102006385.x.CrossRefPubMed
5.
go back to reference Van Everbroeck B, Green A, Pals P, Martin JJ, Cras P: Decreased levels of amyloid-beta 1-42 in cerebrospinal fluid of Creutzfeldt-Jakob disease patients. J Alzheimers Dis. 1999, 1: 419-424.PubMed Van Everbroeck B, Green A, Pals P, Martin JJ, Cras P: Decreased levels of amyloid-beta 1-42 in cerebrospinal fluid of Creutzfeldt-Jakob disease patients. J Alzheimers Dis. 1999, 1: 419-424.PubMed
6.
go back to reference Van Everbroeck B, Green A, Vanmechelen E, Vanderstichele H, Pals P, Sanchez-Valle R, Corrales NC, Martin JJ, Cras P: Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2002, 73: 79-81. 10.1136/jnnp.73.1.79.CrossRefPubMedPubMedCentral Van Everbroeck B, Green A, Vanmechelen E, Vanderstichele H, Pals P, Sanchez-Valle R, Corrales NC, Martin JJ, Cras P: Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2002, 73: 79-81. 10.1136/jnnp.73.1.79.CrossRefPubMedPubMedCentral
7.
go back to reference Otto M, Esselmann H, Schulz-Schaeffer W, Neumann M, Schröter A, Ratzka P, Cepek L, Zerr I, Steinacker P, Windl O, Kornhuber J, Kretzschmar HA, Poser S, Wiltfang J: Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Neurology. 2000, 54 (5): 1099-1102.CrossRefPubMed Otto M, Esselmann H, Schulz-Schaeffer W, Neumann M, Schröter A, Ratzka P, Cepek L, Zerr I, Steinacker P, Windl O, Kornhuber J, Kretzschmar HA, Poser S, Wiltfang J: Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Neurology. 2000, 54 (5): 1099-1102.CrossRefPubMed
8.
go back to reference Van Everbroeck B, Boons J, Cras P: Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease. Clin Neurol Neurosurg. 2005, 107: 355-360. 10.1016/j.clineuro.2004.12.002.CrossRefPubMed Van Everbroeck B, Boons J, Cras P: Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease. Clin Neurol Neurosurg. 2005, 107: 355-360. 10.1016/j.clineuro.2004.12.002.CrossRefPubMed
9.
go back to reference Van Everbroeck BR, Boons J, Cras P: 14-3-3 gamma-isoform detection distinguishes sporadic Creutzfeldt-Jakob disease from other dementias. J Neurol Neurosurg Psychiatry. 2005, 76: 100-102. 10.1136/jnnp.2003.032037.CrossRefPubMedPubMedCentral Van Everbroeck BR, Boons J, Cras P: 14-3-3 gamma-isoform detection distinguishes sporadic Creutzfeldt-Jakob disease from other dementias. J Neurol Neurosurg Psychiatry. 2005, 76: 100-102. 10.1136/jnnp.2003.032037.CrossRefPubMedPubMedCentral
10.
go back to reference Piubelli C, Fiorini M, Zanusso G, Milli A, Fasoli E, Monaco S, Righetti PG: Searching for markers of Creutzfeldt-Jakob disease in cerebrospinal fluid by two-dimensional mapping. Proteomics. 2006, 6 Suppl 1 : 256-261. 10.1002/pmic.200500294.CrossRef Piubelli C, Fiorini M, Zanusso G, Milli A, Fasoli E, Monaco S, Righetti PG: Searching for markers of Creutzfeldt-Jakob disease in cerebrospinal fluid by two-dimensional mapping. Proteomics. 2006, 6 Suppl 1 : 256-261. 10.1002/pmic.200500294.CrossRef
11.
go back to reference Goodall CA, Head MW, Everington D, Ironside JW, Knight RS, Green AJ: Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications. J Neurol Neurosurg Psychiatry. 2006, 77: 89-91. 10.1136/jnnp.2005.065755.CrossRefPubMedPubMedCentral Goodall CA, Head MW, Everington D, Ironside JW, Knight RS, Green AJ: Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications. J Neurol Neurosurg Psychiatry. 2006, 77: 89-91. 10.1136/jnnp.2005.065755.CrossRefPubMedPubMedCentral
12.
go back to reference Van Everbroeck B, Quoilin S, Boons J, Martin JJ, Cras P: A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2003, 74: 1210-1214. 10.1136/jnnp.74.9.1210.CrossRefPubMedPubMedCentral Van Everbroeck B, Quoilin S, Boons J, Martin JJ, Cras P: A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2003, 74: 1210-1214. 10.1136/jnnp.74.9.1210.CrossRefPubMedPubMedCentral
13.
go back to reference Jimi T, Wakayama Y, Shibuya S, Nakata H, Tomaru T, Takahashi Y, Kosaka K, Asano T, Kato K: High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease. Clin Chim Acta. 1992, 211 (1-2): 37-46. 10.1016/0009-8981(92)90103-W.CrossRefPubMed Jimi T, Wakayama Y, Shibuya S, Nakata H, Tomaru T, Takahashi Y, Kosaka K, Asano T, Kato K: High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease. Clin Chim Acta. 1992, 211 (1-2): 37-46. 10.1016/0009-8981(92)90103-W.CrossRefPubMed
14.
go back to reference Brandel JP, Peoc'h K, Beaudry P, Welaratne A, Bottos C, Agid Y, Laplanche JL: 14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients. Ann Neurol. 2001, 49 (2): 257-260. 10.1002/1531-8249(20010201)49:2<257::AID-ANA48>3.0.CO;2-X.CrossRefPubMed Brandel JP, Peoc'h K, Beaudry P, Welaratne A, Bottos C, Agid Y, Laplanche JL: 14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients. Ann Neurol. 2001, 49 (2): 257-260. 10.1002/1531-8249(20010201)49:2<257::AID-ANA48>3.0.CO;2-X.CrossRefPubMed
15.
go back to reference Kropp S, Zerr I, Schulz-Schaeffer WJ, Riedemann C, Bodemer M, Laske C, Kretzschmar HA, Poser S: Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob disease. Neurosci Lett. 1999, 261: 124-126. 10.1016/S0304-3940(98)00992-6.CrossRefPubMed Kropp S, Zerr I, Schulz-Schaeffer WJ, Riedemann C, Bodemer M, Laske C, Kretzschmar HA, Poser S: Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob disease. Neurosci Lett. 1999, 261: 124-126. 10.1016/S0304-3940(98)00992-6.CrossRefPubMed
16.
go back to reference Mollenhauer B, Serafin S, Zerr I, Steinhoff BJ, Otto M, Scherer M, Schul-Schaeffer W, Poser S: Diagnostic problems during late course in Creutzfeldt-Jakob disease. J Neurol. 2003, 250: 629-630. 10.1007/s00415-003-1059-3.CrossRefPubMed Mollenhauer B, Serafin S, Zerr I, Steinhoff BJ, Otto M, Scherer M, Schul-Schaeffer W, Poser S: Diagnostic problems during late course in Creutzfeldt-Jakob disease. J Neurol. 2003, 250: 629-630. 10.1007/s00415-003-1059-3.CrossRefPubMed
17.
go back to reference Zerr I, Pocchiari M, Collins S, Brandel JP, de Pedro Cuesta J, Knight RSG, Bernheimer H, Cardone F, Delasnerie-Lauprêtre N, Cuadrado Corrales N, Ladogana A, Fletcher A, Bodemer M, Awan T, Ruiz Bremón A, Budka H, Laplanche JL, Will RG, Poser S: Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology. 2000, 55: 811-815.CrossRefPubMed Zerr I, Pocchiari M, Collins S, Brandel JP, de Pedro Cuesta J, Knight RSG, Bernheimer H, Cardone F, Delasnerie-Lauprêtre N, Cuadrado Corrales N, Ladogana A, Fletcher A, Bodemer M, Awan T, Ruiz Bremón A, Budka H, Laplanche JL, Will RG, Poser S: Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology. 2000, 55: 811-815.CrossRefPubMed
18.
go back to reference WHO: Human transmissible spongiform encephalopathies. Weekly Epidemiological Record. 1998, 47: 361-365. WHO: Human transmissible spongiform encephalopathies. Weekly Epidemiological Record. 1998, 47: 361-365.
19.
go back to reference Poser S, Mollenhauer B, Krauss A, Zerr I, Steinhoff BJ, Schröter A, Finkenstaedt M, Schulz-Schaeffer W, Kretzschmar HA, Felgenhauer K: How to improve the clinical diagnosis of Creutzfeldt-Jakob disease. Brain. 1999, 122: 2345-2351. 10.1093/brain/122.12.2345.CrossRefPubMed Poser S, Mollenhauer B, Krauss A, Zerr I, Steinhoff BJ, Schröter A, Finkenstaedt M, Schulz-Schaeffer W, Kretzschmar HA, Felgenhauer K: How to improve the clinical diagnosis of Creutzfeldt-Jakob disease. Brain. 1999, 122: 2345-2351. 10.1093/brain/122.12.2345.CrossRefPubMed
20.
go back to reference Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA: Molecular genetics of human prion diseases in Germany. Hum Genet. 1999, 105: 244-252. 10.1007/s004390051096.CrossRefPubMed Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA: Molecular genetics of human prion diseases in Germany. Hum Genet. 1999, 105: 244-252. 10.1007/s004390051096.CrossRefPubMed
21.
go back to reference Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AAF, Trojanowski JQ, Petersen RB, Gambetti P: Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol. 1996, 39 (6): 767-778. 10.1002/ana.410390613.CrossRefPubMed Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AAF, Trojanowski JQ, Petersen RB, Gambetti P: Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol. 1996, 39 (6): 767-778. 10.1002/ana.410390613.CrossRefPubMed
22.
go back to reference Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar HA: Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol. 1999, 46: 224-233. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W.CrossRefPubMed Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar HA: Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol. 1999, 46: 224-233. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W.CrossRefPubMed
23.
go back to reference Otto M, Wiltfang J, Cepek L, Neumann M, Mollenhauer B, Steinacker P, Ciesielczyk B, Schulz-Schaeffer W, Kretzschmar HA, Poser S: Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology. 2002, 58: 192-197.CrossRefPubMed Otto M, Wiltfang J, Cepek L, Neumann M, Mollenhauer B, Steinacker P, Ciesielczyk B, Schulz-Schaeffer W, Kretzschmar HA, Poser S: Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology. 2002, 58: 192-197.CrossRefPubMed
24.
go back to reference Otto M, Stein H, Szudra A, Zerr I, Bodemer M, Gefeller O, Poser S, Kretzschmar HA, Maeder M, Weber T: S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. J Neurol. 1997, 244 (9): 566-570. 10.1007/s004150050145.CrossRefPubMed Otto M, Stein H, Szudra A, Zerr I, Bodemer M, Gefeller O, Poser S, Kretzschmar HA, Maeder M, Weber T: S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. J Neurol. 1997, 244 (9): 566-570. 10.1007/s004150050145.CrossRefPubMed
25.
go back to reference Zerr I, Bodemer M, Kaboth U, Kretzschmar H, Oellerich M, Armstrong VW: Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob disease. Neurosci Lett. 2004, 371: 163-166. 10.1016/j.neulet.2004.08.063.CrossRefPubMed Zerr I, Bodemer M, Kaboth U, Kretzschmar H, Oellerich M, Armstrong VW: Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob disease. Neurosci Lett. 2004, 371: 163-166. 10.1016/j.neulet.2004.08.063.CrossRefPubMed
26.
go back to reference Peoc'h K, Schroder HC, Laplanche J, Ramljak S, Muller WE: Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay. Neurosci Lett. 2001, 301 (3): 167-170. 10.1016/S0304-3940(01)01619-6.CrossRefPubMed Peoc'h K, Schroder HC, Laplanche J, Ramljak S, Muller WE: Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay. Neurosci Lett. 2001, 301 (3): 167-170. 10.1016/S0304-3940(01)01619-6.CrossRefPubMed
27.
go back to reference Volkel D, Zimmermann K, Zerr I, Bodemer M, Lindner T, Turecek PL, Poser S, Schwarz HP: Immunochemical determination of cellular prion protein in plasma from healthy subjects and patients with sporadic CJD or other neurologic diseases. Transfusion. 2001, 41 (4): 441-448. 10.1046/j.1537-2995.2001.41040441.x.CrossRefPubMed Volkel D, Zimmermann K, Zerr I, Bodemer M, Lindner T, Turecek PL, Poser S, Schwarz HP: Immunochemical determination of cellular prion protein in plasma from healthy subjects and patients with sporadic CJD or other neurologic diseases. Transfusion. 2001, 41 (4): 441-448. 10.1046/j.1537-2995.2001.41040441.x.CrossRefPubMed
28.
go back to reference Green AJ, Thompson EJ, Stewart GE, Zeidler M, McKenzie JM, MacLeod MA, Ironside JW, Will RG, Knight RS: Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2001, 70: 744-748. 10.1136/jnnp.70.6.744.CrossRefPubMedPubMedCentral Green AJ, Thompson EJ, Stewart GE, Zeidler M, McKenzie JM, MacLeod MA, Ironside JW, Will RG, Knight RS: Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry. 2001, 70: 744-748. 10.1136/jnnp.70.6.744.CrossRefPubMedPubMedCentral
29.
go back to reference Geschwind M, Martindale J, Miller D, De Armond SJ, Uyehara-Lock J, Gaskin D, Kramer JH, Barbaro NM, Miller BL: Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease. Arch Neurol. 2003, 60: 813-816. 10.1001/archneur.60.6.813.CrossRefPubMed Geschwind M, Martindale J, Miller D, De Armond SJ, Uyehara-Lock J, Gaskin D, Kramer JH, Barbaro NM, Miller BL: Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob disease. Arch Neurol. 2003, 60: 813-816. 10.1001/archneur.60.6.813.CrossRefPubMed
30.
go back to reference Burkhard PR, Sanchez JC, Landis T, Hochstrasser DF: CSF detection of the 14-3-3 protein in unselected patients with dementia. Neurology. 2001, 56 (11): 1528-1533.CrossRefPubMed Burkhard PR, Sanchez JC, Landis T, Hochstrasser DF: CSF detection of the 14-3-3 protein in unselected patients with dementia. Neurology. 2001, 56 (11): 1528-1533.CrossRefPubMed
31.
go back to reference Schaarschmidt H, Prange HW, Reiber H: Neuron-specific enolase concentration in blood as a prognostic parameter in cerebrovascular diseases. Stroke. 1994, 25: 558-565.CrossRefPubMed Schaarschmidt H, Prange HW, Reiber H: Neuron-specific enolase concentration in blood as a prognostic parameter in cerebrovascular diseases. Stroke. 1994, 25: 558-565.CrossRefPubMed
32.
go back to reference Wunderlich MT, Wallesch CW, Goertler M: Release of neurobiochemical markers of brain damage is related to the neurovascular status on admission and the site of arterial occlusion in acute ischemic stroke. J Neurol Sci. 2004, 227: 49-53. 10.1016/j.jns.2004.08.005.CrossRefPubMed Wunderlich MT, Wallesch CW, Goertler M: Release of neurobiochemical markers of brain damage is related to the neurovascular status on admission and the site of arterial occlusion in acute ischemic stroke. J Neurol Sci. 2004, 227: 49-53. 10.1016/j.jns.2004.08.005.CrossRefPubMed
33.
go back to reference Riemenschneider M, Wagenpfeil S, Vanderstichele H, Otto M, Wiltfang J, Kretzschmar H, Vanmechelen E, Förstl H, Kurz A: Phospho-tau/total tau ration in cerebrospinal fluid discriminates Creutzfeldt-Jakob disease from other dementias. Molecular Psychiatry. 2003, 8: 343-347. 10.1038/sj.mp.4001220.CrossRefPubMed Riemenschneider M, Wagenpfeil S, Vanderstichele H, Otto M, Wiltfang J, Kretzschmar H, Vanmechelen E, Förstl H, Kurz A: Phospho-tau/total tau ration in cerebrospinal fluid discriminates Creutzfeldt-Jakob disease from other dementias. Molecular Psychiatry. 2003, 8: 343-347. 10.1038/sj.mp.4001220.CrossRefPubMed
34.
go back to reference Andreasen N, Minthon L, Clarberg A, Davidson P, Gottfries J, Vanmechelen E, Vanderstichele H, Winblad B, Blennow K: Sensitivity, specificity and stability of CSF-tau in AD in a community-based patient sample. Neurology. 1999, 7: 1488-1494.CrossRef Andreasen N, Minthon L, Clarberg A, Davidson P, Gottfries J, Vanmechelen E, Vanderstichele H, Winblad B, Blennow K: Sensitivity, specificity and stability of CSF-tau in AD in a community-based patient sample. Neurology. 1999, 7: 1488-1494.CrossRef
35.
go back to reference Grossman M, Farmer J, Leight S, Work M, Moore P, Van Deerlin V, Pratico D, Clark CM, Branch Coslett H, Chatterjee A, Gee J, Trojanowski JQ, Lee M: Cerebrospinal fluid profile in frontotemporal dementia and Alzheimer's disease. Ann Neurol. 2005, 57 (5): 721-729. 10.1002/ana.20477.CrossRefPubMed Grossman M, Farmer J, Leight S, Work M, Moore P, Van Deerlin V, Pratico D, Clark CM, Branch Coslett H, Chatterjee A, Gee J, Trojanowski JQ, Lee M: Cerebrospinal fluid profile in frontotemporal dementia and Alzheimer's disease. Ann Neurol. 2005, 57 (5): 721-729. 10.1002/ana.20477.CrossRefPubMed
36.
go back to reference Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P: Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology. 2004, 63: 436-442.CrossRefPubMed Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P: Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology. 2004, 63: 436-442.CrossRefPubMed
37.
go back to reference Chen XQ, Fung YW, Yu AC: Association of 14-3-3 gamma and phosphorylated bad attenuates injury in ischemic astrocytes. J Cereb Blood Flow Metab. 2005, 25: 338-347. 10.1038/sj.jcbfm.9600032.CrossRefPubMed Chen XQ, Fung YW, Yu AC: Association of 14-3-3 gamma and phosphorylated bad attenuates injury in ischemic astrocytes. J Cereb Blood Flow Metab. 2005, 25: 338-347. 10.1038/sj.jcbfm.9600032.CrossRefPubMed
38.
go back to reference Kawamoto Y, Akiguchi I, Jarius C, Budka H: Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains. Acta Neuropathol (Berl). 2004, 108: 302-308. 10.1007/s00401-004-0892-5.CrossRef Kawamoto Y, Akiguchi I, Jarius C, Budka H: Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains. Acta Neuropathol (Berl). 2004, 108: 302-308. 10.1007/s00401-004-0892-5.CrossRef
39.
go back to reference Jansen GH, Vogelaar CF, Elshof SM: Distribution of cellular prion protein in normal human cerebral cortex - does it have relevance to Creutzfeldt-Jakob disease?. Clin Chem Lab Med. 2001, 39 (4): 294-298. 10.1515/CCLM.2001.045.CrossRefPubMed Jansen GH, Vogelaar CF, Elshof SM: Distribution of cellular prion protein in normal human cerebral cortex - does it have relevance to Creutzfeldt-Jakob disease?. Clin Chem Lab Med. 2001, 39 (4): 294-298. 10.1515/CCLM.2001.045.CrossRefPubMed
Metadata
Title
Brain-derived proteins in the CSF, do they correlate with brain pathology in CJD?
Authors
Constanze Boesenberg-Grosse
Walter J Schulz-Schaeffer
Monika Bodemer
Barbara Ciesielczyk
Bettina Meissner
Anna Krasnianski
Mario Bartl
Uta Heinemann
Daniela Varges
Sabina Eigenbrod
Hans A Kretzschmar
Alison Green
Inga Zerr
Publication date
01-12-2006
Publisher
BioMed Central
Published in
BMC Neurology / Issue 1/2006
Electronic ISSN: 1471-2377
DOI
https://doi.org/10.1186/1471-2377-6-35

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