Review Article
Will Posttranslational Modifications of Brain Proteins Provide Novel Serological Markers for Dementias?
Table 3
Present fluid biomarkers for dementias from [
15,
33,
42].
| Analysis sample | Biomarker | BIPED classification | Relationship with pathology |
| CSF | t-tau | B,D | Increased in AD, indicates the neuronal degeneration | p-tau | B,D | Increased in AD, reflects the formation of tangles | Aβ42 | B,D | Reduced in the onset stage of AD, it remains unchanged after onset of AD | Aβ oligomers | B,D | Increased in AD | APPs-a | B,D | Soluble APPa is decreased in AD | APPs-β | B,D | APPs-β is a product of APP cleavage by BACE-1; it cannot discriminate normal from AD | APLIβ | B,D | Fragments generated by β- and -secretase are increased in AD | α-Synuclein | B,D | There is an inverse relationship between severity of disease and α-synuclein, it increases rapidly after neuron death in DLB | BACE-1 | B,D | Increased activity in MCI but not AD |
| Plasma | Aβ40,42 | E | Plasma Aβ is in large amount bound to plasma protein, it cannot discriminate normal from AD, but may have a role as an efficacy marker |
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