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@ARTICLE{Knig:257518,
author = {König, A. and Linz, N. and Baykara, E. and Tröger, J. and
Ritchie, C. and Saunders, S. and Teipel, S. and Köhler, S.
and Sánchez-Benavides, G. and Grau-Rivera, O. and Gispert,
J. D. and Palmqvist, S. and Tideman, P. and Hansson, O.},
title = {{S}creening over {S}peech in {U}nselected {P}opulations for
{C}linical {T}rials in {AD} ({PROSPECT}-{AD}): {S}tudy
{D}esign and {P}rotocol.},
journal = {The journal of prevention of Alzheimer's disease},
volume = {10},
number = {2},
issn = {2274-5807},
address = {Cham},
publisher = {Springer International Publishing},
reportid = {DZNE-2023-00429},
pages = {314-321},
year = {2023},
abstract = {Speech impairments are an early feature of Alzheimer's
disease (AD) and consequently, analysing speech performance
is a promising new digital biomarker for AD screening.
Future clinical AD trials on disease modifying drugs will
require a shift to very early identification of individuals
at risk of dementia. Hence, digital markers of language and
speech may offer a method for screening of at-risk
populations that are at the earliest stages of AD,
eventually in combination with advanced machine learning. To
this end, we developed a screening battery consisting of
speech-based neurocognitive tests. The automated test
performs a remote primary screening using a simple
telephone.PROSPECT-AD aims to validate speech biomarkers for
identification of individuals with early signs of AD and
monitor their longitudinal course through access to
well-phenotyped cohorts.PROSPECT-AD leverages ongoing
cohorts such as EPAD (UK), DESCRIBE and DELCODE (Germany),
and BioFINDER Primary Care (Sweden) and Beta-AARC (Spain) by
adding a collection of speech data over the telephone to
existing longitudinal follow-ups. Participants at risk of
dementia are recruited from existing parent cohorts across
Europe to form an AD 'probability-spectrum', i.e.,
individuals with a low risk to high risk of developing AD
dementia. The characterization of cognition, biomarker and
risk factor (genetic and environmental) status of each
research participants over time combined with audio
recordings of speech samples will provide a well-phenotyped
population for comparing novel speech markers with current
gold standard biomarkers and cognitive scores.N= 1000
participants aged 50 or older will be included in total,
with a clinical dementia rating scale (CDR) score of 0 or
0.5. The study protocol is planned to run according to sites
between 12 and 18 months.The speech protocol includes the
following neurocognitive tests which will be administered
remotely: Word List [Memory Function], Verbal Fluency
[Executive Functions] and spontaneous free speech
[Psychological and/ or behavioral symptoms]. Speech features
on the linguistic and paralinguistic level will be extracted
from the recordings and compared to data from CSF and blood
biomarkers, neuroimaging, neuropsychological evaluations,
genetic profiles, and family history. Primary candidate
marker from speech will be a combination of most significant
features in comparison to biomarkers as reference measure.
Machine learning and computational techniques will be
employed to identify the most significant speech biomarkers
that could represent an early indicator of AD pathology.
Furthermore, based on the analysis of speech performances,
models will be trained to predict cognitive decline and
disease progression across the AD continuum.The outcome of
PROSPECT-AD may support AD drug development research as well
as primary or tertiary prevention of dementia by providing a
validated tool using a remote approach for identifying
individuals at risk of dementia and monitoring individuals
over time, either in a screening context or in clinical
trials.},
keywords = {Humans / Alzheimer Disease: psychology / Biomarkers /
Cognitive Dysfunction: psychology / Memory / Speech /
Alzheimer’s disease (Other) / Dementia (Other) / cognitive
assessment (Other) / machine learning (Other) / phone-based
(Other) / screening (Other) / speech biomarker (Other) /
Biomarkers (NLM Chemicals)},
cin = {AG Teipel},
ddc = {610},
cid = {I:(DE-2719)1510100},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
experiment = {EXP:(DE-2719)DELCODE-20140101 /
EXP:(DE-2719)Prospect-AD-20220101 /
EXP:(DE-2719)DESCRIBE-20150101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36946458},
pmc = {pmc:PMC9851094},
doi = {10.14283/jpad.2023.11},
url = {https://pub.dzne.de/record/257518},
}