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Cognitive reserve and rate of change in Alzheimer's and cerebrovascular disease biomarkers among cognitively normal individuals.
Pettigrew, Corinne; Soldan, Anja; Zhu, Yuxin; Cai, Qing; Wang, Mei-Cheng; Moghekar, Abhay; Miller, Michael I; Singh, Baljeet; Martinez, Oliver; Fletcher, Evan; DeCarli, Charles; Albert, Marilyn.
Affiliation
  • Pettigrew C; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: cpettigrew@jhmi.edu.
  • Soldan A; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Zhu Y; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Cai Q; Lyft, Inc., San Francisco, CA, USA.
  • Wang MC; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Moghekar A; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Miller MI; Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.
  • Singh B; Department of Neurology, University of California, Davis, School of Medicine, Davis, CA, USA.
  • Martinez O; Department of Neurology, University of California, Davis, School of Medicine, Davis, CA, USA.
  • Fletcher E; Department of Neurology, University of California, Davis, School of Medicine, Davis, CA, USA.
  • DeCarli C; Department of Neurology, University of California, Davis, School of Medicine, Davis, CA, USA.
  • Albert M; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Neurobiol Aging ; 88: 33-41, 2020 04.
Article in En | MEDLINE | ID: mdl-31932050
ABSTRACT
We examined whether cognitive reserve (CR) impacts level of, or rate of change in, biomarkers of Alzheimer's disease (AD) and small-vessel cerebrovascular disease in >250 individuals who were cognitively normal and middle-aged and older at the baseline. The four primary biomarker categories commonly examined in studies of AD were measured longitudinally cerebrospinal fluid measures of amyloid (A) and tau (T); cerebrospinal fluid and neuroimaging measures of neuronal injury (N); and neuroimaging measures of white matter hyperintensities (WMHs) to assess cerebrovascular pathology (V). CR was indexed by a composite score including years of education, reading, and vocabulary test performance. Higher CR was associated with lower levels of WMHs, particularly among those who subsequently progressed from normal cognition to MCI. CR was not associated with WMH trajectories. In addition, CR was not associated with either levels of, or rate of change in, A/T/N biomarkers. This may suggest that higher CR is associated with lifestyle factors that reduce levels of cerebrovascular disease, allowing individuals with higher CR to better tolerate other types of pathology.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebrovascular Disorders / Cognitive Reserve / Alzheimer Disease Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurobiol Aging Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebrovascular Disorders / Cognitive Reserve / Alzheimer Disease Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurobiol Aging Year: 2020 Document type: Article