-
Je něco špatně v tomto záznamu ?
Bedeutung der Gesamt-tau- und Phospho-tau-Protein-Liquorspiegel in der Demenzdiagnostik
J Hort, M Valis, G Waberzinek, R Talab, L Glossova, M Bojar, M Vyhnalek, D Skoda, J Masopust, P Stourac
Jazyk němčina Země Německo
Typ dokumentu hodnotící studie
NLK
Medline Complete (EBSCOhost)
od 2007-01-01 do Před 1 rokem
- MeSH
- Alzheimerova nemoc krev MeSH
- Creutzfeldtova-Jakobova nemoc krev MeSH
- demence diagnóza krev MeSH
- diferenciální diagnóza MeSH
- fosforylace MeSH
- lidé středního věku MeSH
- lidé MeSH
- proteiny 14-3-3 MeSH
- reprodukovatelnost výsledků MeSH
- senioři MeSH
- senzitivita a specificita MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- hodnotící studie MeSH
BACKGROUND: The diagnosis of Creutzfeldt-Jakob disease (CJD) is based on typical clinical features and can be supported by detection of 14-3-3 protein in the CSF. The present study suggests the importance of investigating this ratio of total tau protein to phosphorylated tau protein in differentiating CJD from other dementias. Thirty-one patients with Alzheimer's disease (AD) or frontotemporal dementia and four with definitive diagnoses of CJD were included in the study. METHODS AND MATERIAL: Results from baseline investigations were compared with those from an age-matched cognitively controlled group with Bell's palsy. Tau protein, phosphorylated tau protein, and beta amyloid were analyzed using a commercially available enzyme-linked immunosorbent assay; 14-3-3 protein was assessed by Western blotting. RESULTS AND CONCLUSION: A distinctly high proportion of total tau protein to phosphorylated tau protein in CSF was found in all patients diagnosed with CJD, even in those with negative 14-3-3 protein blot results. In contrast, marker analysis in patients with Alzheimer's dementia revealed the highest CSF ratio of beta amyloid to phosphorylated tau protein levels. These proteins are important diagnostic biomarkers for CJD, especially in patients with negative 14-3-3 protein findings.
- 000
- 02354naa 2200517 a 4500
- 001
- bmc11006720
- 003
- CZ-PrNML
- 005
- 20121219110146.0
- 008
- 110405s2008 gw e ger||
- 009
- AR
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a ger
- 044 __
- $a gw
- 100 1_
- $a Hort, Jakub, $d 1970- $7 mzk2007386023
- 245 10
- $a Bedeutung der Gesamt-tau- und Phospho-tau-Protein-Liquorspiegel in der Demenzdiagnostik / $c J Hort, M Valis, G Waberzinek, R Talab, L Glossova, M Bojar, M Vyhnalek, D Skoda, J Masopust, P Stourac
- 314 __
- $a 2. Medizinische Fakultat Motol, Neurologische Universitatsklinik der Karls Universitat Prag, Motol, Tschechien.
- 520 9_
- $a BACKGROUND: The diagnosis of Creutzfeldt-Jakob disease (CJD) is based on typical clinical features and can be supported by detection of 14-3-3 protein in the CSF. The present study suggests the importance of investigating this ratio of total tau protein to phosphorylated tau protein in differentiating CJD from other dementias. Thirty-one patients with Alzheimer's disease (AD) or frontotemporal dementia and four with definitive diagnoses of CJD were included in the study. METHODS AND MATERIAL: Results from baseline investigations were compared with those from an age-matched cognitively controlled group with Bell's palsy. Tau protein, phosphorylated tau protein, and beta amyloid were analyzed using a commercially available enzyme-linked immunosorbent assay; 14-3-3 protein was assessed by Western blotting. RESULTS AND CONCLUSION: A distinctly high proportion of total tau protein to phosphorylated tau protein in CSF was found in all patients diagnosed with CJD, even in those with negative 14-3-3 protein blot results. In contrast, marker analysis in patients with Alzheimer's dementia revealed the highest CSF ratio of beta amyloid to phosphorylated tau protein levels. These proteins are important diagnostic biomarkers for CJD, especially in patients with negative 14-3-3 protein findings.
- 650 _2
- $a proteiny 14-3-3 $x mok mozkomíšní $7 D048948
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a Alzheimerova nemoc $x krev $x mok mozkomíšní $7 D000544
- 650 _2
- $a Creutzfeldtova-Jakobova nemoc $x krev $x mok mozkomíšní $7 D007562
- 650 _2
- $a demence $x diagnóza $x krev $x mok mozkomíšní $7 D003704
- 650 _2
- $a diferenciální diagnóza $7 D003937
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a fosforylace $7 D010766
- 650 _2
- $a reprodukovatelnost výsledků $7 D015203
- 650 _2
- $a senzitivita a specificita $7 D012680
- 655 _2
- $a hodnotící studie $7 D023362
- 700 1_
- $a Vališ, Martin, $d 1973- $7 xx0107109
- 700 1_
- $a Waberžinek, Gerhard, $d 1943-2008 $7 nlk19990074052
- 700 1_
- $a Taláb, Radomír, $d 1953- $7 ola2004231499
- 700 1_
- $a Glossová, Ludmila. $7 _AN062290
- 700 1_
- $a Bojar, Martin, $d 1947- $7 jn19990009805
- 700 1_
- $a Vyhnálek, Martin $7 xx0070891
- 700 1_
- $a Škoda, David $7 xx0084481
- 700 1_
- $a Masopust, Jiří, $d 1973- $7 xx0078071
- 700 1_
- $a Štourač, Pavel, $d 1959- $7 xx0060352
- 773 0_
- $t Nervenarzt $w MED00003474 $g Roč. 79, č. 8 (2008), s. 891-892, 894-896, 898 $x 0028-2804
- 910 __
- $a ABA008 $b x $y 7
- 990 __
- $a 20110412125534 $b ABA008
- 991 __
- $a 20121219110228 $b ABA008
- 999 __
- $a ok $b bmc $g 834344 $s 698836
- BAS __
- $a 3
- BMC __
- $a 2008 $b 79 $c 8 $d 891-892, 894-896, 898 $i 0028-2804 $m Nervenarzt $n Nervenarzt $x MED00003474
- LZP __
- $a 2011-4B/ewme