4.5 Article

Evidence of a Relation Between Hippocampal Volume, White Matter Hyperintensities, and Cognition in Subjective Cognitive Decline and Mild Cognitive Impairment

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/geronb/gbz120

关键词

Alzheimer's disease; Biomarkers; Neuroimaging; Neuropsychology

资金

  1. Fonds de recherche du Quebec - Sante (FRQ-S)
  2. Quebec Network for Research on Aging
  3. FRQ-S
  4. Fondation Courtois
  5. Consortium for the Neurodegeneration Associated With Aging (CCNA/CCNV)
  6. Canadian Institutes of Health Research (CIHR) Foundation Grant
  7. CRIUGM
  8. Pfizer Innovation Program

向作者/读者索取更多资源

Objective: The concepts of mild cognitive impairment (MCI) and subjective cognitive decline (SCD) have been proposed to identify individuals in the early stages of Alzheimer's disease (AD), or other neurodegenerative diseases. One approach to validate these concepts is to investigate the relationship between pathological brain markers and cognition in those individuals. Method: We included 126 participants from the Consortium for the Early Identification of Alzheimer's disease-Quebec (CIMA-Q) cohort (67 SCD, 29 MCI, and 30 cognitively healthy controls [CH]). All participants underwent a complete cognitive assessment and structural magnetic resonance imaging. Group comparisons were done using cognitive data, and then correlated with hippocampal volumes and white matter hyperintensities (WMHs). Results: Significant differences were found between participants with MCI and CH on episodic and executive tasks, but no differences were found when comparing SCD and CH. Scores on episodic memory tests correlated with hippocampal volumes in both MCI and SCD, whereas performance on executive tests correlated with WMH in all of our groups. Discussion: As expected, the SCD group was shown to be cognitively healthy on tasks where MCI participants showed impairment. However, SCD's hippocampal volume related to episodic memory performances, and WMH to executive functions. Thus, SCD represents a valid research concept and should be used, alongside MCI, to better understand the preclinical/prodromal phase of AD.

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