Importance Older age, high levels of &bgr;-amyloid (A&bgr;), and the presence of the apolipoprotein E (APOE) &egr;4 allele are risk factors for Alzheimer disease (AD). However, the extent to which… Click to show full abstract
Importance Older age, high levels of &bgr;-amyloid (A&bgr;), and the presence of the apolipoprotein E (APOE) &egr;4 allele are risk factors for Alzheimer disease (AD). However, the extent to which increasing age, A&bgr;, and &egr;4 are associated with memory decline remains unclear, and the age at which memory decline begins for A&bgr;-positive &egr;4 carriers and noncarriers has not been determined. Objective To determine the association of age, A&bgr; level, and APOE &egr;4 with memory decline in a large group of cognitively healthy older adults. Design, Setting, and Participants This longitudinal observational study included cognitively healthy older adults (age >60 years) enrolled in the Australian Imaging, Biomarkers and Lifestyle (AIBL) study from March 31, 2006, through March 31, 2017; of 1583 individuals enrolled, 1136 refused or were excluded owing to other criteria (eg, having mild cognitive impairment or AD). Participants underwent A&bgr; imaging in research clinics in Perth and Melbourne and more than 72 months of follow-up (at 18-month intervals). The association of age with memory was fitted to a quadratic model. Age was treated as a continuous, time-dependent variable. Exposures &bgr;-Amyloid imaging using positron emission tomography, genotyping for APOE [Latin Small Letter Open E]4, and longitudinal neuropsychological assessments of episodic memory during the 72-month follow-up. Main Outcomes and Measures Episodic memory composite score. Results Of the 447 participants, 203 (45.4%) were men and 244 (54.6%) were women; mean (SD) age was 72.5 (6.6) years. Equal proportions of female participants were observed in each A&bgr;-[Latin Small Letter Open E]4 group (24 of 51 A&bgr;-positive &egr;4 noncarriers [47.1%] ; 35 of 64 A&bgr;-negative &egr;4 carriers [54.7%]; 40 of 72 A&bgr;-positive &egr;4 carriers [55.6%]; and 145 of 260 A&bgr;-negative &egr;4 noncarriers [55.8%]). Adults with A&bgr; findings (mean [SD] age, 74.4 [6.8] years) were approximately 4 years older than those negative for A&bgr; (mean [SD] age, 69.8 [6.1] years). Memory decline diverged significantly from A&bgr;-negative [Latin Small Letter Open E]4 noncarriers at an earlier age in A&bgr;-positive [Latin Small Letter Open E]4 carriers (64.5 years) than in A&bgr;-positive [Latin Small Letter Open E]4 noncarriers (76.5 years), such that by 85 years of age, A&bgr;-positive &egr;4 carriers performed approximately 1.5 SD units worse on the episodic memory composite than A&bgr;-negative &egr;4 noncarriers and approximately 0.8 SD units worse than A&bgr;-positive &egr;4 noncarriers. Memory performance of A&bgr;-negative [Latin Small Letter Open E]4 carriers did not differ from that of the A&bgr;-negative [Latin Small Letter Open E]4 noncarriers (estimate [SE], 0.001 [0.001]; tâ=â0.526; Pâ=â.77). Conclusions and Relevance Prior work has shown that A&bgr; and &egr;4 combine to influence memory decline in nondemented older adults. Results of this study indicate that increasing age may further exacerbate these effects. The estimates provided may be used to determine the risk of memory decline associated with A&bgr; and &egr;4 at each age.
               
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