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Classification of sporadic Creutzfeldt-Jakob disease based on clinical and neuropathological characteristics
Author(s) -
José Cortiñas Abrahantes,
Marc Aerts,
Bart Van Everbroeck,
Claude Saegerman,
Dirk Berkvens,
Helena Geys,
Koen Mintiens,
Stefan Roels,
Patrick Cras
Publication year - 2007
Publication title -
european journal of epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.825
H-Index - 111
eISSN - 1573-7284
pISSN - 0393-2990
DOI - 10.1007/s10654-007-9146-x
Subject(s) - medicine , pathology , dementia , disease , neuropathology , myoclonus , transmissible spongiform encephalopathy , degenerative disease , prion protein , scrapie , anesthesia
Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause. Patients are usually aged between 50 and 75 and typical clinical features include rapidly progressive dementia associated with myoclonus and a characteristic electroencephalographic pattern. Neuropathological examination reveals cortical spongiform change, hence the term 'spongiform encephalopathy'. Several statistical techniques were applied to classify patients with sporadic CJD (sCJD), based on clinical and neuropathological investigation. We focus on the classification of neuropathologically confirmed sCJD patients. In order to obtain a classification rule that correctly classifies this type of patients and at the same time controls the overall error rate, we apply several classification techniques, which in general, produce comparable results. The boosting method produces the best results and the variable 14-3-3 protein in cerebrospinal fluid plays the most important role in the prediction of neuropathologically confirmed sCJD.

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