Journal Article DZNE-2021-00066

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Minor neuropsychological deficits in patients with subjective cognitive decline

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2020
Ovid [S.l.]

Neurology 95(9), e1134 - e1143 () [10.1212/WNL.0000000000010142]

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Abstract: Objective: To 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).Method: We 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.Results: We 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.Conclusions: Within 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.

Keyword(s): Aged (MeSH) ; Amyloid beta-Peptides: cerebrospinal fluid (MeSH) ; Case-Control Studies (MeSH) ; Cognitive Dysfunction: cerebrospinal fluid (MeSH) ; Cognitive Dysfunction: physiopathology (MeSH) ; Cognitive Dysfunction: psychology (MeSH) ; Diagnostic Self Evaluation (MeSH) ; Executive Function (MeSH) ; Factor Analysis, Statistical (MeSH) ; Female (MeSH) ; Humans (MeSH) ; Language (MeSH) ; Language Tests (MeSH) ; Learning (MeSH) ; Male (MeSH) ; Memory, Short-Term (MeSH) ; Middle Aged (MeSH) ; Neuropsychological Tests (MeSH) ; Peptide Fragments: cerebrospinal fluid (MeSH) ; Phosphorylation (MeSH) ; Spatial Navigation (MeSH) ; tau Proteins: cerebrospinal fluid (MeSH)

Classification:

Contributing Institute(s):
  1. Neuropsychology (AG Wagner)
  2. Translational Neuropsychiatry (Clinical Study Team Berlin 1 ; AG Priller ; AG Priller)
  3. Clinical Dementia Research (Rostock /Greifswald) (AG Teipel)
  4. Translational Neurodegeneration (AG Höglinger 1)
  5. Cell Biology of Neurological Diseases (AG Jucker)
  6. Delcode (Delcode)
Research Program(s):
  1. 342 - Disease Mechanisms and Model Systems (POF3-342) (POF3-342)
  2. 344 - Clinical and Health Care Research (POF3-344) (POF3-344)
Experiment(s):
  1. Longitudinal Cognitive Impairment and Dementia Study

Appears in the scientific report 2020
Database coverage:
Medline ; Allianz-Lizenz ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; Essential Science Indicators ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > ROS DZNE > ROS DZNE-AG Teipel
Institute Collections > TÜ DZNE > TÜ DZNE-AG Jucker
Institute Collections > BN DZNE > BN DZNE-AG Wagner
Institute Collections > B DZNE > B DZNE-AG Priller
M DZNE-AG Höglinger 1
Public records
Publications Database
M DZNE-Delcode


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Dataset: Minor neuropsychological deficits in patients with subjective cognitive decline
Dryad () [10.5061/dryad.pg4f4qrjp] BibTeX | EndNote: XML, Text | RIS


 Record created 2021-03-23, last modified 2023-09-15



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