| Literature DB >> 32603776 |
Brian J Lopresti1, Elizabeth M Campbell2, Zheming Yu2, Stewart J Anderson3, Ann D Cohen4, Davneet S Minhas2, Beth E Snitz5, Sarah K Royse2, Carl R Becker2, Howard J Aizenstein4, Chester A Mathis2, Oscar L Lopez5, William E Klunk4, Dana L Tudorascu6.
Abstract
To characterize the influence of apolipoprotein-E (APOE) genotype on cerebral Aβ load and longitudinal Aβ trajectories, [11C]Pittsburgh compound-B (PiB) positron emission tomography (PET) imaging was used to assess amyloid load in a clinically heterogeneous cohort of 428 elderly participants with known APOE genotype. Serial [11C]PiB data and a repeated measures model were used to model amyloid trajectories in a subset of 235 participants classified on the basis of APOE genotype. We found that APOE-ε4 was associated with increased Aβ burden and an earlier age of onset of Aβ positivity, whereas APOE-ε2 appeared to have modest protective effects against Aβ. APOE class did not predict rates of Aβ accumulation. The present study suggests that APOE modifies Alzheimer's disease risk through a direct influence on amyloidogenic processes, which manifests as an earlier age of onset of Aβ positivity, although it is likely that other genetic, environmental, and lifestyle factors are important.Entities:
Keywords: Alzheimer's disease; Amyloid; Apolipoprotein-E; Genetics; Positron emission tomography (PET)
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Year: 2020 PMID: 32603776 PMCID: PMC7483397 DOI: 10.1016/j.neurobiolaging.2020.05.012
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673