S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

Journal of Neurology

Volumn 244, Issue 9, 1997, Pages 566-570

  Otto, Markus ^a   Stein, Holger ^a   Szudra, Annemarie ^a,b   Zerr, Inga ^a   Bodemer, Monika ^a   Gefeller, Olaf ^a   Poser, Sigrid ^a   Kretzschmar, Hans A ^a   Mäder, Michael ^a   Weber, Thomas ^a,b  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b Marienkrankenhaus Hamburg   (Germany)

Author keywords

Creutzfeldt Jakob disease; CSF; Protein S 100

Indexed keywords

PROTEIN S 100;

ADULT; AGED; AKINETIC MUTISM; ARTICLE; CEREBELLUM DISEASE; CLINICAL TRIAL; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; ELECTROENCEPHALOGRAM; ENZYME LINKED IMMUNOSORBENT ASSAY; EXTRAPYRAMIDAL SYMPTOM; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MALE; MYOCLONUS; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN CEREBROSPINAL FLUID LEVEL; PYRAMIDAL TRACT; VISUAL DISORDER;

ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS; MALE; MIDDLE AGED; PROSPECTIVE STUDIES; ROC CURVE; S100 PROTEINS;

EID: 9844234269     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050145     Document Type: Article

References (29)

1. Alperovitch A, Brown P, Weber T, Pocchiari M, Hofman A, Will RG (1994) The incidence of Creutzfeldt-Jakob disease in Europe in 1993. Lancet 334:918
2. Bolton DC, McKinley MP, Prusiner SB (1982) Identification of a protein that purifies with the scrapie prion. Science 218:1309-1311
3. Brown DR, Schmidt B, Kretzschmar HA (1996) Role of microglia and host prion protein in neurotoxicity of a prion protein fragment. Nature 380: 345-347
4. Brown P, Cathala F, Raubertas RF, Gajdusek DC, Castaigne P (1987) The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature. Neurology 37:895-904
5. Brown P, Gibbs CJJ, Rodgers-Johnson P, Asher DM, Sulima MP, Bacote A, Goldfarb LG, Gajdusek DC (1994) Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 35:513-529
6. Harrington MG, Merril CR, Asher DM, Gajdusek DC (1986) Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. N Engl J Med 315:279-283
7. Norwich AL, Weissman JS (1997) Deadly conformations: protein misfolding in prion disease. Cell 89: 499-510
8. Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG (1996) The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 335: 924-930
9. Isobe T, Takahashi K, Okuyama T (1984) S100aO (alpha alpha) protein is present in neurons of the central and peripheral nervous system. J Neurochem 43:1494-1496
10. Jensen R, Marshak DR, Anderson C, Lukas TJ, Watterson DM (1985) Characterization of human brain S100 protein fraction: amino acid sequence of S100 beta. J Neurochem 45:700-705
11. Jimi T, Wakayama Y, Shibuya S, Nakata H, Tomaru T, Takahashi Y, Kosaka K, Asano T, Kato K (1992) High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease. Clin Chim Acta 211: 37-46
12. Kindblom LG, Lodding P, Rosengren L, Baudier J, Haglid K (1984) S-100 protein in melanocytic tumors. An immunohistochemical investigation of benign and malignant melanocytic tumors and metastases of malignant melanoma and a characterization of the antigen in comparison to human brain. Acta Pathol Microbiol Immunol Scand A 92:219-230
13. Kretzschmar HA, Ironside J, DeArmond S, Tateishi J (1996) Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch Neurol 53:913-920
14. Liao YC, Lebo RV, Clawson GA, Smuckler EA (1986) Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications. Science 233:364-367
15. Manuelidis L, Fritch W, Xi YG (1997) Evolution of a strain of CJD that induces BSE-like plaques. Science 277: 94-98
16. Masters CL, Harris JO, Gajdusek DC, Gibbs CJJ, Bernoulli C, Asher DM (1979) Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Ann Neurol 5:177-188
17. Oesch B, Westaway D, Walchli M, McKinley MP, Kent SB, Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE, Prusiner SB, Weissmann C (1985) A cellular gene encodes scrapie PrP 27-30 protein. Cell 40:735-746
18. Persson L, Hardemark HG, Gustafsson J, Rundstrom G, Mendel Hartvig I, Esscher T, Pahlman S (1987) S-100 protein and neuron-specific enolase in cerebrospinal fluid and serum: markers of cell damage in human central nervous system. Stroke 18:911-918
19. Prusiner SB (1982) Novel proteinaceous infectious particles cause scrapie. Science 216:136-144
20. Steinhoff BJ, Räcker S, Herrendorf G, Poser S, Grosche S, Zerr I, Kretzschmar H, Weber T (1996) Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol 53:162-165
21. Tagliavini F, Prelli F, Porro M, Salmona M, Bugiani O, Frangione B (1992) A soluble form of prion protein in human cerebrospinal fluid: implications for prion related encephalopathies. Biochem Biophys Res Commun 184:1398-1404
22. Weber T, Zerr I, Bodemer M, Steinhoff BJ, Räcker S, Grosche S, Poser S, Helmhold M, Armstrong VW, Kretzschmar HA (1995) Diagnosis of Creutzfeld-Jakob disease and other human spongiform encephalopathies. J Neurol 242:33
23. Will RG (1996) Surveillance of prion diseases in humans. In: Baker HF, Ridley RM (eds) Prion diseases. Humana Press, Totowa, NJ, pp 119-137
24. Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A, Poser S, Pocchiari M, Hofman A, Smith PG (1996) A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347:921-925
25. Will RG, Zeidler M, Brown P, Harrington M, Lee KH, Kenney KL (1996) Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob disease. Lancet 348:955
26. Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campell TA, Sidle KC, Palmer MS, Collinge J (1996) Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Hum Genet 98:259-264
27. Zerr I, Bodemer M, Otto M, Poser S, Windl O, Kretzschmar HA, Gefeller O, Weber T (1996) Diagnosis of Creutzfeldt-Jakob disease by two dimensional gel electrophoresis of cerebrospinal fluid. Lancet 348:846-849
28. Zerr I, Bodemer M, Räcker S, Grosche S, Poser S, Kretzschmar HA, Weber T (1995) Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease. Lancet 345:1609-1610
29. Zerr I, Bodemer M, Weber T (1997) The 14-3-3 brain protein and transmissible spongiform encephalopathy. N Engl J Med 336:874