4.4 Article

Reaction time and response inhibition in autosomal dominant Alzheimer's disease

Journal

BRAIN AND COGNITION
Volume 147, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bandc.2020.105656

Keywords

Alzheimer's disease; Autosomal dominant; Cognition; Attention; Working memory; Reaction time

Funding

  1. PHS [K08 AG-22228]
  2. Alzheimer's Association New Investigator Research Grant [01-2797, U01 AG-051218]
  3. UCLA Clinical Translational Research Institute [1UL1-RR033176]
  4. Alzheimer's Disease Research Center [P50 AG16570, P50 AG-005142]
  5. General Clinical Research Centers Program [M01-RR00865]
  6. Easton Consortium for Alzheimer's Disease Drug Discovery and Biomarker Development
  7. Shirley and Jack Goldberg Trust

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The study aimed to evaluate attention and working memory in non-demented individuals carrying ADAD mutations using a computerized battery. Results showed that mutation carriers exhibit slower reaction times as they near the age of expected dementia diagnosis, especially on tasks with higher demands on executive function. APOE epsilon 4 status did not impact age-related slowing on cognitive tests in non-carriers or carriers of ADAD mutations.
Objective: Subtle deficits in several cognitive domains characterize the neuropsychological profile of preclinical Alzheimer's disease (AD). Assessment of preclinical individuals with genes causing autosomal dominant AD (ADAD) provides a model for prodromal disease. We sought to sensitively evaluate attention and working memory using a computerized battery in non-demented persons carrying ADAD mutations. Method: A total of 71 non-demented Latinos at-risk for ADAD mutations were recruited [40 mutation carriers (MCs), 31 non-mutation carriers (NCs)] and completed a Spanish language chronometric battery of speeded decision and working memory tasks. Results: On two complex reaction time (RT) tasks involving decision-making and response inhibition, MCs exhibited slower RTs than NCs as they approached their anticipated age of dementia diagnosis. Education moderated these effects, but only in younger MCs. APOE epsilon 4 status was not associated with age-related slowing among NCs or MCs on any of the tests. Conclusions: Our findings indicate MCs respond more slowly as they approach the age of dementia onset on tasks with greater demands on executive function. Our results also suggest these effects were not explained by APOE epsilon 4 status independently of ADAD mutation status. Computerized reaction time tests can provide sensitive measures of the earliest cognitive changes in AD.

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