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Subjective cognitive decline is related to CSF biomarkers of AD in patients with MCI.

Authors :
Wolfsgruber S
Jessen F
Koppara A
Kleineidam L
Schmidtke K
Frölich L
Kurz A
Schulz S
Hampel H
Heuser I
Peters O
Reischies FM
Jahn H
Luckhaus C
Hüll M
Gertz HJ
Schröder J
Pantel J
Rienhoff O
Rüther E
Henn F
Wiltfang J
Maier W
Kornhuber J
Wagner M
Source :
Neurology [Neurology] 2015 Mar 24; Vol. 84 (12), pp. 1261-8. Date of Electronic Publication: 2015 Feb 25.
Publication Year :
2015

Abstract

Objective: 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).<br />Methods: 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.<br />Results: 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.<br />Conclusions: 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.<br /> (© 2015 American Academy of Neurology.)

Details

Language :
English
ISSN :
1526-632X
Volume :
84
Issue :
12
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
25716354
Full Text :
https://doi.org/10.1212/WNL.0000000000001399