Unknown

Dataset Information

0

Cognitively normal APOE ε4 carriers have specific elevation of CSF SNAP-25.


ABSTRACT: Cerebrospinal fluid (CSF) synaptosomal-associated protein 25 (SNAP-25) and neurogranin (Ng) are recently described biomarkers for pre- and postsynaptic integrity known to be elevated in symptomatic Alzheimer disease (AD). Their relationship with Apolipoprotein E (APOE) ε4 carrier status, the major genetic risk factor for AD, remains unclear. In this study, CSF SNAP-25 and Ng were compared in cognitively normal APOE ε4 carriers and noncarriers (n = 274, mean age 65 ± 9.0 years, 39% APOE ε4 carriers, 58% female). CSF SNAP-25, not CSF Ng, was specifically elevated in APOE ε4 carriers versus noncarriers (5.95 ± 1.72 pg/mL, 4.44 ± 1.40 pg/mL, p < 0.0001), even after adjusting for age, sex, years of education, and amyloid status (p < 0.0001). CSF total tau (t-tau), phosphorylated-tau-181 (ptau181), and neurofilament light chain (NfL) also did not vary by APOE ε4 status. Our findings suggest APOE ε4 carriers have amyloid-related and amyloid-independent presynaptic disruption as reflected by elevated CSF SNAP-25 levels. In contrast, postsynaptic disruption as reflected by elevations in CSF neurogranin is related to amyloid status.

SUBMITTER: Butt OH 

PROVIDER: S-EPMC8793109 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


Cerebrospinal fluid (CSF) synaptosomal-associated protein 25 (SNAP-25) and neurogranin (Ng) are recently described biomarkers for pre- and postsynaptic integrity known to be elevated in symptomatic Alzheimer disease (AD). Their relationship with Apolipoprotein E (APOE) ε4 carrier status, the major genetic risk factor for AD, remains unclear. In this study, CSF SNAP-25 and Ng were compared in cognitively normal APOE ε4 carriers and noncarriers (n = 274, mean age 65 ± 9.0 years, 39% APOE ε4 carrie  ...[more]

Similar Datasets

| S-EPMC8842835 | biostudies-literature
| S-EPMC7609923 | biostudies-literature
| S-EPMC5968505 | biostudies-literature
| S-EPMC8283833 | biostudies-literature
| S-EPMC6547570 | biostudies-literature
| S-EPMC9074716 | biostudies-literature
| S-EPMC11667521 | biostudies-literature
| S-EPMC6601608 | biostudies-literature
| S-EPMC5333781 | biostudies-literature
| S-EPMC6610620 | biostudies-literature