Minor neuropsychological deficits in patients with subjective cognitive decline

OBJECTIVETo determine the nature and extent of minor neuropsychological deficits in patients with subjective cognitive decline (SCD) and their association with CSF biomarkers of Alzheimer disease (AD). METHODWe analyzed data from n = 449 cognitively normal participants (n = 209 healthy controls, n =...

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Veröffentlicht in:Neurology 2020-09, Vol.95 (9), p.e1134-e1143
Hauptverfasser: Wolfsgruber, Steffen, Kleineidam, Luca, Guski, Jannis, Polcher, Alexandra, Frommann, Ingo, Roeske, Sandra, Spruth, Eike Jakob, Franke, Christiana, Priller, Josef, Kilimann, Ingo, Teipel, Stefan, Buerger, Katharina, Janowitz, Daniel, Laske, Christoph, Buchmann, Martina, Peters, Oliver, Menne, Felix, Fuentes Casan, Manuel, Wiltfang, Jens, Bartels, Claudia, Düzel, Emrah, Metzger, Coraline, Glanz, Wenzel, Thelen, Manuela, Spottke, Annika, Ramirez, Alfredo, Kofler, Barbara, Fließbach, Klaus, Schneider, Anja, Heneka, Michael T., Brosseron, Frederic, Meiberth, Dix, Jessen, Frank, Wagner, Michael
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Sprache:eng
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Zusammenfassung:OBJECTIVETo determine the nature and extent of minor neuropsychological deficits in patients with subjective cognitive decline (SCD) and their association with CSF biomarkers of Alzheimer disease (AD). METHODWe analyzed data from n = 449 cognitively normal participants (n = 209 healthy controls, n = 240 patients with SCD) from an interim data release of the German Center for Neurodegenerative Diseases Longitudinal Cognitive Impairment and Dementia Study (DELCODE). An extensive neuropsychological test battery was applied at baseline for which we established a latent, 5 cognitive domain factor structure comprising learning and memory, executive functions, language abilities, working memory, and visuospatial functions. We compared groups in terms of global and domain-specific performance and correlated performance with different CSF markers of AD pathology. RESULTSWe observed worse performance (Cohen d = ≈0.25–0.5, adjusted for age, sex differences with analysis of covariance) in global performance, memory, executive functions, and language abilities for the SCD group compared to healthy controls. In addition, worse performance in these domains was moderately (r = ≈0.3) associated with lower CSF β-amyloid42/40 and CSF β-amyloid42/phosphorylated tau181 in the whole sample and specifically in the SCD subgroup. CONCLUSIONSWithin the spectrum of clinically unimpaired (i.e., before mild cognitive impairment) cognitive performance, SCD is associated with minor deficits in memory, executive function, and language abilities. The association of these subtle cognitive deficits with AD CSF biomarkers speaks to their validity and potential use for the early detection of underlying preclinical AD.
ISSN:0028-3878
1526-632X
DOI:10.1212/WNL.0000000000010142