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@ARTICLE{Wolfsgruber:137844,
author = {Wolfsgruber, Steffen and Jessen, Frank and Koppara,
Alexander and Kleineidam, Luca and Schmidtke, Klaus and
Frölich, Lutz and Kurz, Alexander and Schulz, Stefanie and
Hampel, Harald and Heuser, Isabella and Peters, Oliver and
Reischies, Friedel M and Jahn, Holger and Luckhaus,
Christian and Hüll, Michael and Gertz, Hermann-Josef and
Schröder, Johannes and Pantel, Johannes and Rienhoff, Otto
and Rüther, Eckart and Henn, Fritz and Wiltfang, Jens and
Maier, Wolfgang and Kornhuber, Johannes and Wagner, Michael},
title = {{S}ubjective cognitive decline is related to {CSF}
biomarkers of {AD} in patients with {MCI}.},
journal = {Neurology},
volume = {84},
number = {12},
issn = {0028-3878},
address = {[S.l.]},
publisher = {Ovid},
reportid = {DZNE-2020-04166},
pages = {1261-1268},
year = {2015},
abstract = {To test whether, in individuals with mild cognitive
impairment (MCI), different measures of subjective cognitive
decline (SCD) in the memory domain predict abnormal CSF
biomarkers of Alzheimer disease (AD).We analyzed the
multicenter baseline (cross-sectional) data of 245 patients
with MCI. SCD was measured quantitatively with the
Subjective Memory Decline Scale (SMDS) and qualitatively by
assessing particular concerns associated with
self-experienced worsening of memory. Logistic regression
models were used to examine associations between SCD and
abnormal CSF biomarkers, taking into account objective
memory impairment, depressive symptoms, and education as
covariates.Abnormal CSF β-amyloid 1-42 (Aβ42) and more
depressive symptoms were associated with higher SMDS scores
and with the report of memory concerns. Risk of abnormal CSF
Aβ42 increased by an estimated $57\%$ for a 1-SD increase
in SMDS scores and was doubled in patients who had SMDS
scores >4 or who reported memory concerns, respectively. In
addition, both SCD measures predicted risk of having a
biomarker signature indicative of prodromal AD defined as
presence of low CSF Aβ42 together with either high CSF tau
or CSF phosphorylated tau 181 levels.In MCI, specific
aspects of SCD severity and quality are related to CSF
biomarkers indicative of AD. This extends findings in
pre-MCI samples and calls for an improved operational
assessment of SCD in MCI. This might be useful for sample
enrichment strategies for increased likelihood of AD
pathology.},
keywords = {Aged / Aged, 80 and over / Alzheimer Disease: cerebrospinal
fluid / Alzheimer Disease: physiopathology / Alzheimer
Disease: psychology / Amyloid beta-Peptides: cerebrospinal
fluid / Biomarkers: cerebrospinal fluid / Cognitive
Dysfunction: cerebrospinal fluid / Cognitive Dysfunction:
physiopathology / Cognitive Dysfunction: psychology / Female
/ Humans / Male / Memory Disorders: cerebrospinal fluid /
Memory Disorders: physiopathology / Memory Disorders:
psychology / Middle Aged / Peptide Fragments: cerebrospinal
fluid / Prodromal Symptoms / tau Proteins: cerebrospinal
fluid / Amyloid beta-Peptides (NLM Chemicals) / Biomarkers
(NLM Chemicals) / Peptide Fragments (NLM Chemicals) /
amyloid beta-protein (1-42) (NLM Chemicals) / tau Proteins
(NLM Chemicals)},
cin = {AG Wagner / AG Jessen / U Clinical Researchers - Bonn},
ddc = {610},
cid = {I:(DE-2719)1011201 / I:(DE-2719)1011102 /
I:(DE-2719)7000001},
pnm = {344 - Clinical and Health Care Research (POF3-344)},
pid = {G:(DE-HGF)POF3-344},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:25716354},
doi = {10.1212/WNL.0000000000001399},
url = {https://pub.dzne.de/record/137844},
}