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. 2011 Oct 4;11:120. doi: 10.1186/1471-2377-11-120

Table 2.

Analysis of Western blots method and ELISA of 14-3-3 protein of CSF in 124 CJD patients and 99 patients with other neurological disorders and rapid progressive dementia

disease number male female 14-3-3 γ 14-3-3 all isoforms
ELISA WB WB
average SD min max
CJD 124 69 55 263, 549 21, 525 135 75, 373 108/124 114/124
DAT 54 33 21 1, 537 751.2 0 2, 410 3/54 7/54
CVD 7 5 2 975.9 332.4 521 1, 51 2 0/7 2/7
PD 5 4 1 542.2 20.3 521 565 0/5 0/5
PSP 3 2 1 223.3 226.6 38 476 0/3 0/3
FTLD 2 1 1 425 236.2 258 592 0/2 0/2
HD 1 1 0 556 0. 556 556 0/1 0/1
CBD 2 2 0 449.5 245.4 276 623 0/2 0/2
ALS 3 1 2 303.7 184.8 179 516 0/3 0/3
limbic encephalitis 2 1 1 4440.5 1935.4 3, 072 5, 809 2/2 2/2
MELAS 4 2 2 5, 069.5 222.7 4, 912 5, 227 4/4 4/4
PCD/LEMS 2 1 1 4, 387 217.8 4, 233 4, 541 2/2 2/2
temporal epilepsy 4 1 3 3, 356.8 1332.4 1, 530 4, 696 4/4 4/4
MCI 3 1 2 603 20.8 591 627 0/3 0/3
Dementia, etiology unknown 3 1 2 410.3 150.5 258 559 0/3 0/3
healthy subject 4 2 2 0 0 0 0 0/4 0/4

CJD: Creutzfeldt-Jakob disease, DAT: Dementia of Alzheimer's type, CVD: Cerebral Vascular Disorder, PD: Parkinson's disease, PSP: progressive supranuclear palsy, FTLD: frontotemporal lobular degeneration HD: Huntington's disease, CBD: corticobasal degeneration, ALS: amyotrophic lateral sclerosis, MELAS: Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, Stroke-like episodes, PCD: paraneoplastic cerebellar degeneration, LEMS: Lambert-Eaton myasthenic syndrome, MCI: mild cognitive impairment,