Autopsy-diagnosed neurodegenerative dementia cases support the use of cerebrospinal fluid protein biomarkers in the diagnostic work-up
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
34035398
PubMed Central
PMC8149718
DOI
10.1038/s41598-021-90366-5
PII: 10.1038/s41598-021-90366-5
Knihovny.cz E-zdroje
- MeSH
- amyloidní beta-protein mozkomíšní mok MeSH
- biologické markery mozkomíšní mok MeSH
- demence mozkomíšní mok klasifikace diagnóza MeSH
- diferenciální diagnóza MeSH
- DNA vazebné proteiny mozkomíšní mok MeSH
- lidé středního věku MeSH
- lidé MeSH
- neurofilamentové proteiny mozkomíšní mok MeSH
- peptidové fragmenty mozkomíšní mok MeSH
- pitva MeSH
- progranuliny mozkomíšní mok MeSH
- proteiny 14-3-3 mozkomíšní mok MeSH
- proteiny tau mozkomíšní mok MeSH
- proteiny v mozkomíšním moku mozkomíšní mok MeSH
- regulace genové exprese MeSH
- retrospektivní studie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- senzitivita a specificita MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- amyloid beta-protein (1-42) MeSH Prohlížeč
- amyloidní beta-protein MeSH
- biologické markery MeSH
- DNA vazebné proteiny MeSH
- GRN protein, human MeSH Prohlížeč
- MAPT protein, human MeSH Prohlížeč
- neurofilament protein L MeSH Prohlížeč
- neurofilamentové proteiny MeSH
- peptidové fragmenty MeSH
- progranuliny MeSH
- proteiny 14-3-3 MeSH
- proteiny tau MeSH
- proteiny v mozkomíšním moku MeSH
- TARDBP protein, human MeSH Prohlížeč
Various proteins play a decisive role in the pathology of different neurodegenerative diseases. Nonetheless, most of these proteins can only be detected during a neuropathological assessment, although some non-specific biomarkers are routinely tested for in the cerebrospinal fluid (CSF) as a part of the differential diagnosis of dementia. In antemortem CSF samples from 117 patients with different types of neuropathologically confirmed neurodegenerative disease with dementia, we assessed total-tau (t-tau), phosphorylated-tau (181P) (p-tau), amyloid-beta (1-42) (Aβ42), TAR DNA binding protein (TDP)-43, progranulin (PGRN), and neurofilament light (NfL) chain levels, and positivity of protein 14-3-3. We found t-tau levels and the t-tau/p-tau ratios were significantly higher in prion diseases compared to the other neurodegenerative diseases. Statistically significant differences in the t-tau/Aβ42 ratio predominantly corresponded to t-tau levels in prion diseases and Aβ42 levels in AD. TDP-43 levels were significantly lower in prion diseases. Additionally, the TDP-43/Aβ42 ratio was better able to distinguish Alzheimer's disease from other neurodegenerative diseases compared to using Aβ42 alone. In frontotemporal lobar degeneration, PRGN levels were significantly higher in comparison to other neurodegenerative diseases. There is an increasing need for biomarkers suitable for diagnostic workups for neurodegenerative diseases. It appears that adding TDP-43 and PGRN to the testing panel for neurodegenerative diseases could improve the resolution of differential diagnoses.
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