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Cerebrospinal fluid (CSF) features of neuropathological changes (ADNC) in Alzheimer's disease (ADNC) include a decrease
Figure 1: Cover art of the paper
Because of their sensitivity to the neuropathological process of AD, these CSF biomarkers can be used in life to stratify AD patients with individuals without AD, including suspected non-AD pathophysiology (SNAP
It is not yet known how the accompanying αSyn affects CSF, which is a problem with any CSF-based strategies for detecting AD, including the t-tau/Aβ42 ratio
As a result, αSyn may affect CSF biomarkers in a different way than ADNC, affecting diagnostic accuracy and interpretation
To address this, Katheryn Alexandra Quilico Cousins of the University of Pennsylvania and others compared CSF Aβ42, p-tau181, t-tau, and Ng levels of autopsy-confirmed AD and AD mixed with αSyn (AD+αSyn); We used αSyn and non-impaired control groups without ADNC as reference groups
The main goal is to test whether the AD CSF biomarker differs
They next tested a direct association
Inclusion criteria were neuropathological diagnosis of AD, mixed AD+αSyn, and αSyn
Participants had 61 AD, 39 AD+αSyn hybrids, 20 αSyn, and 61 controls
Figure 2: Graph of the paper results
The analysis of variance showed that the p-tau181 (F(1,94) = 17, p=0), t-t-tau (F(1,93) = 11, p=0.
αSyn is not a significant factor in Aβ42 (p=1
The results showed that the accompanying pathological changes in αSyn in AD patients were associated with lower CSF p-tau181, t-t-tau, and Ng levels, and could affect the diagnostic accuracy