The diagnosis of diseases causing memory difficulties or dementia is often challenging.
Without the use of advanced methods such as cerebrospinal fluid tests, approximately
25-30% do not receive a correct diagnosis today. However, the investigators have recently
developed new blood biomarkers with high diagnostic accuracy, and the investigators now
want to investigate whether they can eventually replace cerebrospinal fluid tests. This
is because blood tests are much more cost-effective and significantly easier for patients
compared to cerebrospinal fluid tests.
In this study, 1200 patients undergoing clinical evaluations at the Memory Clinic, Skåne
University Hospital in Malmö, are included for blood and cerebrospinal fluid sample
collection. The blood samples are sent for analysis using the new blood biomarkers.
Subsequently, the results are compared with those from the clinical analysis of
cerebrospinal fluid to determine how well they perform in routine clinical practice as an
alternative to cerebrospinal fluid tests and whether the blood test improves patient
care. This comparison is carried out by the attending physician in three steps:
Assessment without access to the results of either the blood test or cerebrospinal
fluid test.
Assessment with access to only the results of the blood test.
Assessment with access to the results of both the blood test and cerebrospinal fluid
test.
Aim 1) To prospectively validate plasma AD biomarkers for diagnosis of patients with
cognitive symptoms who are evaluated in a specialist memory clinic. The investigators
here intend to study the clinical robustness and accuracy of plasma AD biomarkers in
real-world settings by using high-performing plasma assays over 2-3 years, focusing on a
specialist memory clinic population (n=1200). In this study plasma samples are collected
as part of clinical praxis and analyzed on a bi-weekly basis throughout the study period
(and not in single batches/at study closure). The investigators will (1) use pre-defined
cut offs for each biomarker (similar to real world clinical practice), and (2) use an
accurate reference standard (i.e., presence of AD brain pathology as determined with
cerebrospinal fluid (CSF) Aβ42/Aβ40 [Lumipulse; Fujirebio] and CSF P-tau217 [Eli Lilly]).
The investigators will strive to recruit diverse and representative populations of
patients with subjective cognitive decline (SCD), mild cognitive impairment (MCI) and
mild dementia. The effects of potential confounders (such as kidney function) on
diagnostic accuracy will also be studied. The investigators will only use really
top-performing plasma assays for each biomarker, including p-tau217 and Ab42/Ab40.
Expected outcomes: The investigators will 1) determine the diagnostic accuracy of
different plasma AD biomarkers, 2) establish an optimal combination of plasma biomarkers
for detection of AD brain pathology and 3) identify the effects of different potential
confounding factors (e.g., kidney function) on the performance of different plasma
biomarkers, when used prospectively in both real-world specialist and primary care
populations.
Aim 2) Determine whether blood AD biomarkers improve patient management in specialist
memory clinic settings. As often noted by regulatory authorities, it is important to know
if novel diagnostic methods improve the actual management of patients in real world
settings. Consequently, the investigators study whether the most promising plasma
biomarkers for symptomatic AD (including plasma p-tau217) will improve AD diagnosis
beyond what is currently done as part of clinical practice. The dementia experts will
document the most likely diagnosis (and the certainty of the diagnosis) after having
performed an interview with the patient and informant, as well as evaluated the patient's
cognitive test results, routine blood tests and structural brain imaging. The physician
will then re-evaluate the diagnosis (and certainty of diagnosis) after having obtained
the plasma p-tau217 results, and the pre- and posttest diagnosis will be compared to the
reference standard (i.e., presence of AD brain pathology as determined with CSF Aβ42/Aβ40
[Lumipulse; Fujirebio] and CSF P-tau217 [Eli Lilly]). Change in treatment and care of the
patient after evaluating the p-tau217 results will also be recorded similar to how
amyloid-positron emission tomography (PET) was evaluated in the IDEAS study.
Expected outcomes: The investigators will determine whether the addition of plasma AD
biomarkers to current clinical practice in memory clinics and/or primary care improves
diagnosis and management of patients with SCD, MCI or mild dementia.