A comparison between tau and amyloid‐b cerebrospinal fluid biomarkers in chronic traumatic encephalopathy and Alzheimer disease. (31st December 2021)

• Record Type: Journal Article
• Authors: Turk, Katherine W.; Geada, Alexandra W.; Alvarez, Victor E.; Xia, Weiming; Cherry, Jonathan D.; Huber, Bertrand R.; Mez, Jesse; Alosco, Michael L.; Meng, Gaoyuan; Nicks, Raymond W.; Tripodis, Yorghos; Budson, Andrew; Dwyer, Brigid; Kowall, Neil W.; Cantu, Robert; Goldstein, Lee E.; Katz, Douglas I.; Stern, Robert A.; McKee, Ann C.; Stein, Thor D.
• Is Part Of: Alzheimer's & dementia. Volume 17(2021)Supplement 5
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-12-31
• Subjects: Alzheimer's disease -- Periodicals; Alzheimer Disease -- Periodicals; Dementia -- Periodicals; Démence; Maladie d'Alzheimer; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.83
• DOI: 10.1002/alz.051392
• Languages: English
• ISSNs: 1552-5260

Abstract

Abstract: Background: Cerebrospinal fluid (CSF) tau and beta‐amyloid levels in chronic traumatic encephalopathy (CTE), a disease which can be clinically indistinguishable from Alzheimer's disease (AD), are largely unknown. We examined postmortem CSF analytes among participants with autopsy confirmed CTE and AD. Method: A total of 192 participants from the Boston University AD Center and VA‐BU‐CLF Center had post‐mortem CSF collected at autopsy. Participants were divided into pathological groups based on consensus AD and CTE criteria, resulting in 61 participants with CTE (18 low, 43 high stage), 79 participants with AD (23 low, 56 intermediate to high pathological change), 11 participants with concurrent CTE and AD, and 41 participants lacking both CTE and AD neuropathology. The Meso Scale Discovery immunoassay system was utilized to measure amyloid‐beta (Ab1‐40, Ab1‐42 ), total tau (t‐tau), and phosphorylated tau (p‐tau181 and p‐tau231 ). Result: The low CTE group had higher levels of p‐tau231 compared no CTE/no AD (p=0.041), and compared to the low AD group (p=0.018). The low CTE group had lower levels of Aβ1‐42 compared to no CTE/no AD (p=0.016). The high CTE group had higher levels of p‐tau231 compared to AD (p=0.025) and lower levels of Aβ1‐42 compared to the AD group (p=0.015). Importantly, p‐tau231 and Aβ1‐42 were predictors of diagnosis of CTE vs. no CTE/no AD and CTE vs. AD (Figure 1). Conclusion: Increased CSF p‐tau231 is a promising potentially sensitive biomarkers of CTE and decreased CSF Aβ1‐42 in CTE warrants further investigation as to underlying mechanism and potential as an additional CTE biomarker.