Learning slopes in early-onset Alzheimer's disease

the LEADS Consortium

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

OBJECTIVE: Investigation of learning slopes in early-onset dementias has been limited. The current study aimed to highlight the sensitivity of learning slopes to discriminate disease severity in cognitively normal participants and those diagnosed with early-onset dementia with and without β-amyloid positivity. METHOD: Data from 310 participants in the Longitudinal Early-Onset Alzheimer's Disease Study (aged 41 to 65) were used to calculate learning slope metrics. Learning slopes among diagnostic groups were compared, and the relationships of slopes with standard memory measures were determined. RESULTS: Worse learning slopes were associated with more severe disease states, even after controlling for demographics, total learning, and cognitive severity. A particular metric—the learning ratio (LR)—outperformed other learning slope calculations across analyses. CONCLUSIONS: Learning slopes appear to be sensitive to early-onset dementias, even when controlling for the effect of total learning and cognitive severity. The LR may be the learning measure of choice for such analyses. Highlights: Learning is impaired in amyloid-positive EOAD, beyond cognitive severity scores alone. Amyloid-positive EOAD participants perform worse on learning slopes than amyloid-negative participants. Learning ratio appears to be the learning metric of choice for EOAD participants.

Original languageEnglish (US)
Pages (from-to)S19-S28
JournalAlzheimer's and Dementia
Volume19
Issue numberS9
DOIs
StatePublished - Nov 2023

Funding

We would like to thank all members of the LEADS Consortium, as well as the LEADS Clinical Outcomes group, and Constantine Gatsonis, PhD, for his statistical guidance. This study is generously supported by Alzheimer's Association AARG-22-926940, Alzheimer's Association LDRFP-21-818464, R56 AG057195, NIA U01AG6057195, NIA U24AG021886, Alzheimer's Association LEADS GENETICS-19-639372, NIA U01 AG016976, NIA P30 AG010133, NIA P50 AG008702, NIA P50 AG025688, NIA P50 AG005146, NIA P30 AG062421, NIA P30 AG062422, NIA P50 AG023501, NIA P30 AG010124, NIA P30AG066506, NIA P30 AG013854, NIA P50 AG005681, NIA P50AG047366, and NIA U24AG021886. We would like to thank all members of the LEADS Consortium, as well as the LEADS Clinical Outcomes group, and Constantine Gatsonis, PhD, for his statistical guidance. This study is generously supported by Alzheimer's Association AARG‐22‐926940, Alzheimer's Association LDRFP‐21‐818464, R56 AG057195, NIA U01AG6057195, NIA U24AG021886, Alzheimer's Association LEADS GENETICS‐19‐639372, NIA U01 AG016976, NIA P30 AG010133, NIA P50 AG008702, NIA P50 AG025688, NIA P50 AG005146, NIA P30 AG062421, NIA P30 AG062422, NIA P50 AG023501, NIA P30 AG010124, NIA P30AG066506, NIA P30 AG013854, NIA P50 AG005681, NIA P50AG047366, and NIA U24AG021886.

Keywords

  • early-onset Alzheimer's disease
  • learning slopes
  • memory

ASJC Scopus subject areas

  • Epidemiology
  • Health Policy
  • Developmental Neuroscience
  • Clinical Neurology
  • Geriatrics and Gerontology
  • Cellular and Molecular Neuroscience
  • Psychiatry and Mental health

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