CSF Aβ and tau biomarkers in cognitively unimpaired Aβ- middle-aged and older APOE ε4 carriers.

Neurobiol Aging

Turner Institute of Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia; Cogstate Ltd., Melbourne, Australia.

Published: September 2023

This study aimed to determine the relationship between the apolipoprotein E (APOE) ε4 allele and cerebrospinal fluid (CSF) and neuroimaging biomarkers of Alzheimer's disease, and cognition in cognitively unimpaired (CU) middle-aged adults (n = 82; M = 58.2), and in Aβ- CU older adults (n = 71; M = 71.8). Aβ- CU middle-aged ε4 carriers showed lower CSF Aβ levels, higher levels of CSF total tau (t-tau) and neurofilament light (NfL), and poorer cognitive performance compared to noncarriers (Cohen's d: 0.30-0.56). In Aβ- CU older adults, ε4 carriers also had lower CSF Aβ levels and higher levels of CSF t-tau and p-tau181, compared to noncarriers (Cohen's d: 0.65-0.74). In both Aβ- middle-aged and older adults, hippocampal and total brain volume were equivalent between ε4 carriers and noncarriers. In Aβ- CU middle-aged adults, APOE ε4 is associated with decreased levels of Aβ, increased tau and NfL, and poorer cognition. Similar relationships were observed in Aβ- CU older adults. These results have implications for understanding clinicopathological relationships between APOE ε4 and the emergence of cognitive and biomarker abnormalities in Aβ- adults.

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Source
http://dx.doi.org/10.1016/j.neurobiolaging.2023.05.009DOI Listing

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