Skip to main content
Top
Published in: BMC Neurology 1/2011

Open Access 01-12-2011 | Research article

Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study

Authors: Michael B Coulthart, Gerard H Jansen, Elina Olsen, Deborah L Godal, Tim Connolly, Bernard CK Choi, Zheng Wang, Neil R Cashman

Published in: BMC Neurology | Issue 1/2011

Login to get access

Abstract

Background

To better characterize the value of cerebrospinal fluid (CSF) proteins as diagnostic markers in a clinical population of subacute encephalopathy patients with relatively low prevalence of sporadic Creutzfeldt-Jakob disease (sCJD), we studied the diagnostic accuracies of several such markers (14-3-3, tau and S100B) in 1000 prospectively and sequentially recruited Canadian patients with clinically suspected sCJD.

Methods

The study included 127 patients with autopsy-confirmed sCJD (prevalence = 12.7%) and 873 with probable non-CJD diagnoses. Standard statistical measures of diagnostic accuracy were employed, including sensitivity (Se), specificity (Sp), predictive values (PVs), likelihood ratios (LRs), and Receiver Operating Characteristic (ROC) analysis.

Results

At optimal cutoff thresholds (empirically selected for 14-3-3, assayed by immunoblot; 976 pg/mL for tau and 2.5 ng/mL for S100B, both assayed by ELISA), Se and Sp respectively were 0.88 (95% CI, 0.81-0.93) and 0.72 (0.69-0.75) for 14-3-3; 0.91 (0.84-0.95) and 0.88 (0.85-0.90) for tau; and 0.87 (0.80-0.92) and 0.87 (0.84-0.89) for S100B. The observed differences in Sp between 14-3-3 and either of the other 2 markers were statistically significant. Positive LRs were 3.1 (2.8-3.6) for 14-3-3; 7.4 (6.9-7.8) for tau; and 6.6 (6.1-7.1) for S100B. Negative LRs were 0.16 (0.10-0.26) for 14-3-3; 0.10 (0.06-0.20) for tau; and 0.15 (0.09-0.20) for S100B. Estimates of areas under ROC curves were 0.947 (0.931-0.961) for tau and 0.908 (0.888-0.926) for S100B. Use of interval LRs (iLRs) significantly enhanced accuracy for patient subsets [e.g., 41/120 (34.2%) of tested sCJD patients displayed tau levels > 10,000 pg/mL, with an iLR of 56.4 (22.8-140.0)], as did combining tau and S100B [e.g., for tau > 976 pg/mL and S100B > 2.5 ng/mL, positive LR = 18.0 (12.9-25.0) and negative LR = 0.02 (0.01-0.09)].

Conclusions

CSF 14-3-3, tau and S100B proteins are useful diagnostic markers of sCJD even in a low-prevalence clinical population. CSF tau showed better overall diagnostic accuracy than 14-3-3 or S100B. Reporting of quantitative assay results and combining tau with S100B could enhance case definitions used in diagnosis and surveillance of sCJD.
Appendix
Available only for authorised users
Literature
1.
go back to reference Knight R: Creutzfeldt-Jakob disease: a rare cause of dementia in elderly persons. Clin Infect Dis. 2006, 43 (3): 340-346. 10.1086/505215.CrossRefPubMed Knight R: Creutzfeldt-Jakob disease: a rare cause of dementia in elderly persons. Clin Infect Dis. 2006, 43 (3): 340-346. 10.1086/505215.CrossRefPubMed
2.
go back to reference Belay ED, Schonberger LB: The public health impact of prion diseases. Annu Rev Public Health. 2005, 26: 191-212. 10.1146/annurev.publhealth.26.021304.144536.CrossRefPubMed Belay ED, Schonberger LB: The public health impact of prion diseases. Annu Rev Public Health. 2005, 26: 191-212. 10.1146/annurev.publhealth.26.021304.144536.CrossRefPubMed
4.
go back to reference Ladogana A, Puopolo M, Croes EA, Budka H, Jarius C, Collins S, Klug GM, Sutcliffe T, Giulivi A, Alperovitch A, Delasnerie-Laupretre N, Brandel JP, Poser S, Kretzschmar H, Rietveld I, Mitrova E, Cuesta Jde P, Martinez-Martin P, Glatzel M, Aguzzi A, Knight R, Ward H, Pocchiari M, van Duijn CM, Will RG, Zerr I: Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology. 2005, 64 (9): 1586-1591. 10.1212/01.WNL.0000160117.56690.B2.CrossRefPubMed Ladogana A, Puopolo M, Croes EA, Budka H, Jarius C, Collins S, Klug GM, Sutcliffe T, Giulivi A, Alperovitch A, Delasnerie-Laupretre N, Brandel JP, Poser S, Kretzschmar H, Rietveld I, Mitrova E, Cuesta Jde P, Martinez-Martin P, Glatzel M, Aguzzi A, Knight R, Ward H, Pocchiari M, van Duijn CM, Will RG, Zerr I: Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology. 2005, 64 (9): 1586-1591. 10.1212/01.WNL.0000160117.56690.B2.CrossRefPubMed
5.
go back to reference Parchi P, Strammiello R, Giese A, Kretzschmar H: Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. Acta Neuropathol. 2011, 121 (1): 91-112. 10.1007/s00401-010-0779-6.CrossRefPubMed Parchi P, Strammiello R, Giese A, Kretzschmar H: Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. Acta Neuropathol. 2011, 121 (1): 91-112. 10.1007/s00401-010-0779-6.CrossRefPubMed
6.
go back to reference Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, DeArmond SJ, Barbaro NM, Martindale J, Miller BL, Geschwind MD: First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006, 66 (2): 286-287.CrossRefPubMed Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, DeArmond SJ, Barbaro NM, Martindale J, Miller BL, Geschwind MD: First symptom in sporadic Creutzfeldt-Jakob disease. Neurology. 2006, 66 (2): 286-287.CrossRefPubMed
8.
go back to reference Murray K: Creutzfeldt-Jacob disease mimics, or how to sort out the subacute encephalopathy patient. Pract Neurol. 2011, 11 (1): 19-28. 10.1136/jnnp.2010.235721.CrossRefPubMed Murray K: Creutzfeldt-Jacob disease mimics, or how to sort out the subacute encephalopathy patient. Pract Neurol. 2011, 11 (1): 19-28. 10.1136/jnnp.2010.235721.CrossRefPubMed
9.
go back to reference Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, Breithaupt M, Varges D, Meissner B, Ladogana A, Schuur M, Haik S, Collins SJ, Jansen GH, Stokin GB, Pimentel J, Hewer E, Collie D, Smith P, Roberts H, Brandel JP, van Duijn C, Pocchiari M, Begue C, Cras P, Will RG, Sanchez-Juan P: Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009, 132 (Pt 10): 2659-2668.CrossRefPubMedPubMedCentral Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, Breithaupt M, Varges D, Meissner B, Ladogana A, Schuur M, Haik S, Collins SJ, Jansen GH, Stokin GB, Pimentel J, Hewer E, Collie D, Smith P, Roberts H, Brandel JP, van Duijn C, Pocchiari M, Begue C, Cras P, Will RG, Sanchez-Juan P: Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain. 2009, 132 (Pt 10): 2659-2668.CrossRefPubMedPubMedCentral
10.
go back to reference Atarashi R, Satoh K, Sano K, Fuse T, Yamaguchi N, Ishibashi D, Matsubara T, Nakagaki T, Yamanaka H, Shirabe S, Yamada M, Mizusawa H, Kitamoto T, Klug G, McGlade A, Collins SJ, Nishida N: Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. Nat Med. 2011, 17 (2): 175-178. 10.1038/nm.2294.CrossRefPubMed Atarashi R, Satoh K, Sano K, Fuse T, Yamaguchi N, Ishibashi D, Matsubara T, Nakagaki T, Yamanaka H, Shirabe S, Yamada M, Mizusawa H, Kitamoto T, Klug G, McGlade A, Collins SJ, Nishida N: Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. Nat Med. 2011, 17 (2): 175-178. 10.1038/nm.2294.CrossRefPubMed
11.
go back to reference Edgeworth JA, Farmer M, Sicilia A, Tavares P, Beck J, Campbell T, Lowe J, Mead S, Rudge P, Collinge J, Jackson GS: Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay. Lancet. 2011, 377 (9764): 487-493. 10.1016/S0140-6736(10)62308-2.CrossRefPubMed Edgeworth JA, Farmer M, Sicilia A, Tavares P, Beck J, Campbell T, Lowe J, Mead S, Rudge P, Collinge J, Jackson GS: Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay. Lancet. 2011, 377 (9764): 487-493. 10.1016/S0140-6736(10)62308-2.CrossRefPubMed
12.
go back to reference Kovacs GG, Voigtlander T, Gelpi E, Budka H: Rationale for diagnosing human prion disease. World J Biol Psychiatry. 2004, 5 (2): 83-91. 10.1080/15622970410029916.CrossRefPubMed Kovacs GG, Voigtlander T, Gelpi E, Budka H: Rationale for diagnosing human prion disease. World J Biol Psychiatry. 2004, 5 (2): 83-91. 10.1080/15622970410029916.CrossRefPubMed
13.
go back to reference Sanchez-Juan P, Green A, Ladogana A, Cuadrado-Corrales N, Saanchez-Valle R, Mitrovaa E, Stoeck K, Sklaviadis T, Kulczycki J, Hess K, Bodemer M, Slivarichova D, Saiz A, Calero M, Ingrosso L, Knight R, Janssens AC, van Duijn CM, Zerr I: CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology. 2006, 67 (4): 637-643. 10.1212/01.wnl.0000230159.67128.00.CrossRefPubMed Sanchez-Juan P, Green A, Ladogana A, Cuadrado-Corrales N, Saanchez-Valle R, Mitrovaa E, Stoeck K, Sklaviadis T, Kulczycki J, Hess K, Bodemer M, Slivarichova D, Saiz A, Calero M, Ingrosso L, Knight R, Janssens AC, van Duijn CM, Zerr I: CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology. 2006, 67 (4): 637-643. 10.1212/01.wnl.0000230159.67128.00.CrossRefPubMed
14.
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 (2): 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 (2): 192-197.CrossRefPubMed
15.
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 (9): 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 (9): 1210-1214. 10.1136/jnnp.74.9.1210.CrossRefPubMedPubMedCentral
16.
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
17.
go back to reference Geschwind MD, Martindale J, Miller D, DeArmond 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 (6): 813-816. 10.1001/archneur.60.6.813.CrossRefPubMed Geschwind MD, Martindale J, Miller D, DeArmond 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 (6): 813-816. 10.1001/archneur.60.6.813.CrossRefPubMed
18.
go back to reference Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG: The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med. 1996, 335 (13): 924-930. 10.1056/NEJM199609263351303.CrossRefPubMed Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG: The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med. 1996, 335 (13): 924-930. 10.1056/NEJM199609263351303.CrossRefPubMed
19.
go back to reference Klug GM, Wand H, Boyd A, Law M, Whyte S, Kaldor J, Masters CL, Collins S: Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster. Brain. 2009, 132 (Pt 2): 493-501.PubMed Klug GM, Wand H, Boyd A, Law M, Whyte S, Kaldor J, Masters CL, Collins S: Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster. Brain. 2009, 132 (Pt 2): 493-501.PubMed
20.
go back to reference Sackett DL, Haynes RB, Tugwell P, Guyatt GH: Clinical Epidemiology: A Basic Science for Clinical Medicine. 1991, Lippincott Williams & Wilkins, 2 Sackett DL, Haynes RB, Tugwell P, Guyatt GH: Clinical Epidemiology: A Basic Science for Clinical Medicine. 1991, Lippincott Williams & Wilkins, 2
21.
go back to reference Grimes DA, Schulz KF: Refining clinical diagnosis with likelihood ratios. Lancet. 2005, 365 (9469): 1500-1505. 10.1016/S0140-6736(05)66422-7.CrossRefPubMed Grimes DA, Schulz KF: Refining clinical diagnosis with likelihood ratios. Lancet. 2005, 365 (9469): 1500-1505. 10.1016/S0140-6736(05)66422-7.CrossRefPubMed
22.
go back to reference Chohan G, Pennington C, Mackenzie JM, Andrews M, Everington D, Will RG, Knight RS, Green AJ: The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review. J Neurol Neurosurg Psychiatry. 2010, 81 (11): 1243-1248. 10.1136/jnnp.2009.197962.CrossRefPubMed Chohan G, Pennington C, Mackenzie JM, Andrews M, Everington D, Will RG, Knight RS, Green AJ: The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review. J Neurol Neurosurg Psychiatry. 2010, 81 (11): 1243-1248. 10.1136/jnnp.2009.197962.CrossRefPubMed
23.
go back to reference Coulthart MB, Jansen GH, Olsen E, Godal DL, Connolly T, Choi BCK, Wang Z, Cashman NR: CSF proteins and diagnosis of sporadic Creutzfeldt-Jakob disease in Canada [abstract]. Prion. 2011, 5: s126-CrossRef Coulthart MB, Jansen GH, Olsen E, Godal DL, Connolly T, Choi BCK, Wang Z, Cashman NR: CSF proteins and diagnosis of sporadic Creutzfeldt-Jakob disease in Canada [abstract]. Prion. 2011, 5: s126-CrossRef
24.
go back to reference Altman DG, Machin D, Bryant TN, Gardner MJ: Statistics with Confidence. 2000 Altman DG, Machin D, Bryant TN, Gardner MJ: Statistics with Confidence. 2000
25.
go back to reference Crawford JR, Garthwaite PH, Betkowska K: Bayes' theorem and diagnostic tests in neuropsychology: interval estimates for post-test probabilities. Clin Neuropsychol. 2009, 23 (4): 624-644. 10.1080/13854040802524229.CrossRefPubMed Crawford JR, Garthwaite PH, Betkowska K: Bayes' theorem and diagnostic tests in neuropsychology: interval estimates for post-test probabilities. Clin Neuropsychol. 2009, 23 (4): 624-644. 10.1080/13854040802524229.CrossRefPubMed
27.
go back to reference Peduzzi P, Concato J, Kemper E, Holford TR, Feinstein AR: A simulation study of the number of events per variable in logistic regression analysis. J Clin Epidemiol. 1996, 49 (12): 1373-1379. 10.1016/S0895-4356(96)00236-3.CrossRefPubMed Peduzzi P, Concato J, Kemper E, Holford TR, Feinstein AR: A simulation study of the number of events per variable in logistic regression analysis. J Clin Epidemiol. 1996, 49 (12): 1373-1379. 10.1016/S0895-4356(96)00236-3.CrossRefPubMed
28.
go back to reference Bowden SC, Loring DW: The diagnostic utility of multiple-level likelihood ratios. J Int Neuropsychol Soc. 2009, 15 (5): 769-776. 10.1017/S1355617709990373.CrossRefPubMed Bowden SC, Loring DW: The diagnostic utility of multiple-level likelihood ratios. J Int Neuropsychol Soc. 2009, 15 (5): 769-776. 10.1017/S1355617709990373.CrossRefPubMed
29.
go back to reference Beaudry P, Cohen P, Brandel JP, Delasnerie-Laupretre N, Richard S, Launay JM, Laplanche JL: 14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord. 1999, 10 (1): 40-46. 10.1159/000017095.CrossRefPubMed Beaudry P, Cohen P, Brandel JP, Delasnerie-Laupretre N, Richard S, Launay JM, Laplanche JL: 14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Dement Geriatr Cogn Disord. 1999, 10 (1): 40-46. 10.1159/000017095.CrossRefPubMed
30.
go back to reference Lemstra AW, van Meegen MT, Vreyling JP, Meijerink PH, Jansen GH, Bulk S, Baas F, van Gool WA: 14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients. Neurology. 2000, 55 (4): 514-516.CrossRefPubMed Lemstra AW, van Meegen MT, Vreyling JP, Meijerink PH, Jansen GH, Bulk S, Baas F, van Gool WA: 14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients. Neurology. 2000, 55 (4): 514-516.CrossRefPubMed
31.
go back to reference Collins S, Boyd A, Fletcher A, Gonzales M, McLean CA, Byron K, Masters CL: Creutzfeldt-Jakob disease: diagnostic utility of 14-3-3 protein immunodetection in cerebrospinal fluid. J Clin Neurosci. 2000, 7 (3): 203-208. 10.1054/jocn.1999.0193.CrossRefPubMed Collins S, Boyd A, Fletcher A, Gonzales M, McLean CA, Byron K, Masters CL: Creutzfeldt-Jakob disease: diagnostic utility of 14-3-3 protein immunodetection in cerebrospinal fluid. J Clin Neurosci. 2000, 7 (3): 203-208. 10.1054/jocn.1999.0193.CrossRefPubMed
32.
go back to reference Aksamit AJ, Preissner CM, Homburger HA: Quantitation of 14-3-3 and neuron-specific enolase proteins in CSF in Creutzfeldt-Jakob disease. Neurology. 2001, 57 (4): 728-730.CrossRefPubMed Aksamit AJ, Preissner CM, Homburger HA: Quantitation of 14-3-3 and neuron-specific enolase proteins in CSF in Creutzfeldt-Jakob disease. Neurology. 2001, 57 (4): 728-730.CrossRefPubMed
33.
go back to reference Satoh K, Shirabe S, Eguchi H, Tsujino A, Eguchi K, Satoh A, Tsujihata M, Niwa M, Katamine S, Kurihara S, Matsuo H: 14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan. Cell Mol Neurobiol. 2006, 26 (1): 45-52. 10.1007/s10571-006-9370-z.CrossRefPubMed Satoh K, Shirabe S, Eguchi H, Tsujino A, Eguchi K, Satoh A, Tsujihata M, Niwa M, Katamine S, Kurihara S, Matsuo H: 14-3-3 protein, total tau and phosphorylated tau in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease and neurodegenerative disease in Japan. Cell Mol Neurobiol. 2006, 26 (1): 45-52. 10.1007/s10571-006-9370-z.CrossRefPubMed
34.
go back to reference Cuadrado-Corrales N, Jimenez-Huete A, Albo C, Hortiguela R, Vega L, Cerrato L, Sierra-Moros M, Rabano A, de Pedro-Cuesta J, Calero M: Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD. BMC Neurol. 2006, 6: 25-10.1186/1471-2377-6-25.CrossRefPubMedPubMedCentral Cuadrado-Corrales N, Jimenez-Huete A, Albo C, Hortiguela R, Vega L, Cerrato L, Sierra-Moros M, Rabano A, de Pedro-Cuesta J, Calero M: Impact of the clinical context on the 14-3-3 test for the diagnosis of sporadic CJD. BMC Neurol. 2006, 6: 25-10.1186/1471-2377-6-25.CrossRefPubMedPubMedCentral
35.
go back to reference Skinningsrud A, Stenset V, Gundersen AS, Fladby T: Cerebrospinal fluid markers in Creutzfeldt-Jakob disease. Cerebrospinal Fluid Res. 2008, 5: 14-10.1186/1743-8454-5-14.CrossRefPubMedPubMedCentral Skinningsrud A, Stenset V, Gundersen AS, Fladby T: Cerebrospinal fluid markers in Creutzfeldt-Jakob disease. Cerebrospinal Fluid Res. 2008, 5: 14-10.1186/1743-8454-5-14.CrossRefPubMedPubMedCentral
36.
go back to reference Baldeiras IE, Ribeiro MH, Pacheco P, Machado A, Santana I, Cunha L, Oliveira CR: Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients. J Neurol. 2009, 256 (9): 1540-1550. 10.1007/s00415-009-5160-0.CrossRefPubMed Baldeiras IE, Ribeiro MH, Pacheco P, Machado A, Santana I, Cunha L, Oliveira CR: Diagnostic value of CSF protein profile in a Portuguese population of sCJD patients. J Neurol. 2009, 256 (9): 1540-1550. 10.1007/s00415-009-5160-0.CrossRefPubMed
37.
go back to reference Goncalves CA, Leite MC, Nardin P: Biological and methodological features of the measurement of S100B, a putative marker of brain injury. Clin Biochem. 2008, 41 (10-11): 755-763. 10.1016/j.clinbiochem.2008.04.003.CrossRefPubMed Goncalves CA, Leite MC, Nardin P: Biological and methodological features of the measurement of S100B, a putative marker of brain injury. Clin Biochem. 2008, 41 (10-11): 755-763. 10.1016/j.clinbiochem.2008.04.003.CrossRefPubMed
38.
go back to reference Scott IA, Greenberg PB, Poole PJ: Cautionary tales in the clinical interpretation of studies of diagnostic tests. Intern Med J. 2008, 38 (2): 120-129. 10.1111/j.1445-5994.2007.01436.x.CrossRefPubMed Scott IA, Greenberg PB, Poole PJ: Cautionary tales in the clinical interpretation of studies of diagnostic tests. Intern Med J. 2008, 38 (2): 120-129. 10.1111/j.1445-5994.2007.01436.x.CrossRefPubMed
39.
go back to reference Ladogana A, Sanchez-Juan P, Mitrova E, Green A, Cuadrado-Corrales N, Sanchez-Valle R, Koscova S, Aguzzi A, Sklaviadis T, Kulczycki J, Gawinecka J, Saiz A, Calero M, van Duijn CM, Pocchiari M, Knight R, Zerr I: Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies. J Neurol. 2009, 256 (10): 1620-1628. 10.1007/s00415-009-5163-x.CrossRefPubMedPubMedCentral Ladogana A, Sanchez-Juan P, Mitrova E, Green A, Cuadrado-Corrales N, Sanchez-Valle R, Koscova S, Aguzzi A, Sklaviadis T, Kulczycki J, Gawinecka J, Saiz A, Calero M, van Duijn CM, Pocchiari M, Knight R, Zerr I: Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies. J Neurol. 2009, 256 (10): 1620-1628. 10.1007/s00415-009-5163-x.CrossRefPubMedPubMedCentral
40.
go back to reference Schoonenboom NS, Mulder C, Vanderstichele H, Van Elk EJ, Kok A, Van Kamp GJ, Scheltens P, Blankenstein MA: Effects of processing and storage conditions on amyloid beta (1-42) and tau concentrations in cerebrospinal fluid: implications for use in clinical practice. Clin Chem. 2005, 51 (1): 189-195.CrossRefPubMed Schoonenboom NS, Mulder C, Vanderstichele H, Van Elk EJ, Kok A, Van Kamp GJ, Scheltens P, Blankenstein MA: Effects of processing and storage conditions on amyloid beta (1-42) and tau concentrations in cerebrospinal fluid: implications for use in clinical practice. Clin Chem. 2005, 51 (1): 189-195.CrossRefPubMed
41.
go back to reference Willis BH: Spectrum bias--why clinicians need to be cautious when applying diagnostic test studies. Fam Pract. 2008, 25 (5): 390-396. 10.1093/fampra/cmn051.CrossRefPubMed Willis BH: Spectrum bias--why clinicians need to be cautious when applying diagnostic test studies. Fam Pract. 2008, 25 (5): 390-396. 10.1093/fampra/cmn051.CrossRefPubMed
42.
go back to reference Mulherin SA, Miller WC: Spectrum bias or spectrum effect? Subgroup variation in diagnostic test evaluation. Ann Intern Med. 2002, 137 (7): 598-602.CrossRefPubMed Mulherin SA, Miller WC: Spectrum bias or spectrum effect? Subgroup variation in diagnostic test evaluation. Ann Intern Med. 2002, 137 (7): 598-602.CrossRefPubMed
43.
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
44.
go back to reference Kenney K, Brechtel C, Takahashi H, Kurohara K, Anderson P, Gibbs CJ: An enzyme-linked immunosorbent assay to quantify 14-3-3 proteins in the cerebrospinal fluid of suspected Creutzfeldt-Jakob disease patients. Ann Neurol. 2000, 48 (3): 395-398. 10.1002/1531-8249(200009)48:3<395::AID-ANA18>3.0.CO;2-A.CrossRefPubMed Kenney K, Brechtel C, Takahashi H, Kurohara K, Anderson P, Gibbs CJ: An enzyme-linked immunosorbent assay to quantify 14-3-3 proteins in the cerebrospinal fluid of suspected Creutzfeldt-Jakob disease patients. Ann Neurol. 2000, 48 (3): 395-398. 10.1002/1531-8249(200009)48:3<395::AID-ANA18>3.0.CO;2-A.CrossRefPubMed
45.
go back to reference Leuck J, Peoch K, Laplanche JL, Grabar E, Muller WE, Schroder HC: A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients. Cell Mol Biol (Noisy-le-grand). 2000, 46 (7): 1291-1296. Leuck J, Peoch K, Laplanche JL, Grabar E, Muller WE, Schroder HC: A novel binding assay for detection of 14-3-3 protein in cerebrospinal fluid from Creutzfeldt-Jakob patients. Cell Mol Biol (Noisy-le-grand). 2000, 46 (7): 1291-1296.
46.
go back to reference Gmitterova K, Heinemann U, Bodemer M, Krasnianski A, Meissner B, Kretzschmar HA, Zerr I: 14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes. Neurobiol Aging. 2009, 30 (11): 1842-1850. 10.1016/j.neurobiolaging.2008.01.007.CrossRefPubMed Gmitterova K, Heinemann U, Bodemer M, Krasnianski A, Meissner B, Kretzschmar HA, Zerr I: 14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes. Neurobiol Aging. 2009, 30 (11): 1842-1850. 10.1016/j.neurobiolaging.2008.01.007.CrossRefPubMed
47.
go back to reference Orru CD, Wilham JM, Raymond LD, Kuhn F, Schroeder B, Raeber AJ, Caughey B: Prion disease blood test using immunoprecipitation and improved quaking-induced conversion. MBio. 2011, 2 (3): Print 2011 Orru CD, Wilham JM, Raymond LD, Kuhn F, Schroeder B, Raeber AJ, Caughey B: Prion disease blood test using immunoprecipitation and improved quaking-induced conversion. MBio. 2011, 2 (3): Print 2011
48.
go back to reference Singh A, Beveridge AJ, Singh N: Decreased CSF transferrin in sCJD: a potential pre-mortem diagnostic test for prion disorders. PLoS One. 2011, 6 (3): e16804-10.1371/journal.pone.0016804.CrossRefPubMedPubMedCentral Singh A, Beveridge AJ, Singh N: Decreased CSF transferrin in sCJD: a potential pre-mortem diagnostic test for prion disorders. PLoS One. 2011, 6 (3): e16804-10.1371/journal.pone.0016804.CrossRefPubMedPubMedCentral
49.
go back to reference Brechlin P, Jahn O, Steinacker P, Cepek L, Kratzin H, Lehnert S, Jesse S, Mollenhauer B, Kretzschmar HA, Wiltfang J, Otto M: Cerebrospinal fluid-optimized two-dimensional difference gel electrophoresis (2-D DIGE) facilitates the differential diagnosis of Creutzfeldt-Jakob disease. Proteomics. 2008, 8 (20): 4357-4366. 10.1002/pmic.200800375.CrossRefPubMed Brechlin P, Jahn O, Steinacker P, Cepek L, Kratzin H, Lehnert S, Jesse S, Mollenhauer B, Kretzschmar HA, Wiltfang J, Otto M: Cerebrospinal fluid-optimized two-dimensional difference gel electrophoresis (2-D DIGE) facilitates the differential diagnosis of Creutzfeldt-Jakob disease. Proteomics. 2008, 8 (20): 4357-4366. 10.1002/pmic.200800375.CrossRefPubMed
Metadata
Title
Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study
Authors
Michael B Coulthart
Gerard H Jansen
Elina Olsen
Deborah L Godal
Tim Connolly
Bernard CK Choi
Zheng Wang
Neil R Cashman
Publication date
01-12-2011
Publisher
BioMed Central
Published in
BMC Neurology / Issue 1/2011
Electronic ISSN: 1471-2377
DOI
https://doi.org/10.1186/1471-2377-11-133

Other articles of this Issue 1/2011

BMC Neurology 1/2011 Go to the issue