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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

From: High sensitivity of an ELISA kit for detection of the gamma-isoform of 14-3-3 proteins: usefulness in laboratory diagnosis of human prion disease

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

  1. 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,