<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pichet Binette A</submitter><funding>NIA NIH HHS</funding><funding>Alzheimer Society</funding><funding>Foundation for the National Institutes of Health</funding><funding>Alzheimer&amp;apos;s Association</funding><funding>Canadian Institutes of Health Research</funding><pagination>776-785</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7415608</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>89(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Major prevention trials for Alzheimer's disease (AD) are now focusing on multidomain lifestyle interventions. However, the exact combination of behavioral factors related to AD pathology remains unclear. In 2 cohorts of cognitively unimpaired individuals at risk of AD, we examined which combinations of personality traits, neuropsychiatric symptoms, and cognitive lifestyle (years of education or lifetime cognitive activity) related to the pathological hallmarks of AD, amyloid-β, and tau deposits.&lt;h4>Methods&lt;/h4>A total of 115 older adults with a parental or multiple-sibling family history of sporadic AD (PREVENT-AD [PRe-symptomatic EValuation of Experimental or Novel Treatments for AD] cohort) underwent amyloid and tau positron emission tomography and answered several que</pubmed_abstract><journal>Biological psychiatry</journal><pubmed_title>Amyloid and Tau Pathology Associations With Personality Traits, Neuropsychiatric Symptoms, and Cognitive Lifestyle in the Preclinical Phases of Sporadic and Autosomal Dominant Alzheimer's Disease.</pubmed_title><pmcid>PMC7415608</pmcid><funding_grant_id>R01 AG052550</funding_grant_id><funding_grant_id>UF1 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However, the exact combination of behavioral factors related to AD pathology remains unclear. In 2 cohorts of cognitively unimpaired individuals at risk of AD, we examined which combinations of personality traits, neuropsychiatric symptoms, and cognitive lifestyle (years of education or lifetime cognitive activity) related to the pathological hallmarks of AD, amyloid-β, and tau deposits.&lt;h4>Methods&lt;/h4>A total of 115 older adults with a parental or multiple-sibling family history of sporadic AD (PREVENT-AD [PRe-symptomatic EValuation of Experimental or Novel Treatments for AD] cohort) underwent amyloid and tau positron emission tomography and answered several que</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-05-02T22:41:41.184Z</modification><creation>2025-04-05T18:20:48.39Z</creation></dates><accession>S-EPMC7415608</accession><cross_references><pubmed>32228870</pubmed><doi>10.1016/j.biopsych.2020.01.023</doi></cross_references></HashMap>