Cerebrospinal fluid (CSF)
biomarkers have been increasingly studied for
dementia diagnosis, however the accuracy to distinguish between different forms of
dementia is still unsatisfactory. In this study, the added value of another CSF Aβ-
peptide (Aβ40), along with the core CSF markers t-Tau, p-Tau, and Aβ42, in the discrimination between two large
dementia groups of
Frontotemporal Lobar Degeneration (
FTLD; n=107),
Alzheimer's Disease (AD; n=107) and non-demented subjects (n=33) was evaluated. In
FTLD, t-Tau and p-Tau were significantly increased in relation to controls, but lower than in AD, while Aβ42 was similar in
FTLD and controls, but higher than in AD. Equally reduced Aβ40 levels were seen in both
dementia groups, and therefore the combination of Aβ40 with core CSF
biomarkers optimally discriminated
FTLD and AD patients from controls. Aβ42 and t-Tau were selected as the best
biomarker subset to differentiate
FTLD from AD, with no added value of Aβ40 to the model. Diagnostic accuracy between
FTLD and AD was still sub-optimal, with a significant percentage (23%) of
FTLD patients, in particularly women, carrying an ApoE-ε4 allele, showing a CSF-AD
biomarkers profile. Although CSF Aβ40 does not appear to have an additional value in the distinction between
FTLD and AD, it increases the discrimination between subjects with
dementia from controls. A CSF-AD
biomarker profile can be seen in patients with a clinical phenotype of
FTLD, reinforcing the need for autopsy confirmation.