Soares Carolina, Bellaver Bruna, Ferreira Pamela C L, Povala Guilherme, Schaffer Aguzzoli Cristiano, Ferrari-Souza João Pedro, Zalzale Hussein, Lussier Firoza Z, Rohden Francieli, Abbas Sarah, Bauer-Negrini Guilherme, Teixeira Leffa Douglas, Benedet Andréa Lessa, Langhough Rebecca, Betthauser Tobey J, Christian Bradley T, Wilson Rachael E, L Tudorascu Dana, Rosa-Neto Pedro, Karikari Thomas K, Zetterberg Henrik, Blennow Kaj, Zimmer Eduardo R, Johnson Sterling C, Pascoal Tharick A
Department of Psychiatry, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Graduate Program in Biological Sciences: Biochemistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Nat Commun. 2025 Aug 29;16(1):8076. doi: 10.1038/s41467-025-63545-5.
Cerebrospinal fluid (CSF) total tau (t-tau) is considered a biomarker of neuronal degeneration alongside brain atrophy and fluid neurofilament light chain protein (NfL) in biomarker models of Alzheimer's disease (AD). However, previous studies show that CSF t-tau correlates strongly with synaptic dysfunction/degeneration biomarkers like neurogranin (Ng) and synaptosomal-associated protein 25 (SNAP25). Here, we compare the association between CSF t-tau and synaptic degeneration and axonal/neuronal degeneration biomarkers in cognitively unimpaired and impaired groups from two independent cohorts. We observe a stronger correlation between CSF t-tau and synaptic biomarkers than neurodegeneration biomarkers in both groups. Synaptic biomarkers explain a greater proportion of variance in CSF t-tau levels compared to neurodegeneration biomarkers. Notably, CSF t-tau levels are elevated in individuals with abnormalities only in synaptic biomarkers, but not in individuals with abnormalities only in neurodegeneration biomarkers. Our findings suggest that CSF t-tau is a closer proxy for synaptic degeneration than for axonal/neuronal degeneration.
在阿尔茨海默病(AD)的生物标志物模型中,脑脊液(CSF)总tau蛋白(t-tau)与脑萎缩和脑脊液神经丝轻链蛋白(NfL)一样,被视为神经元变性的生物标志物。然而,先前的研究表明,脑脊液t-tau与突触功能障碍/变性生物标志物(如神经颗粒素(Ng)和突触体相关蛋白25(SNAP25))密切相关。在这里,我们比较了来自两个独立队列的认知未受损和受损组中脑脊液t-tau与突触变性以及轴突/神经元变性生物标志物之间的关联。我们观察到,在两组中,脑脊液t-tau与突触生物标志物之间的相关性比与神经变性生物标志物之间的相关性更强。与神经变性生物标志物相比,突触生物标志物在脑脊液t-tau水平的变异中解释了更大的比例。值得注意的是,仅突触生物标志物异常的个体脑脊液t-tau水平升高,而仅神经变性生物标志物异常的个体脑脊液t-tau水平未升高。我们的研究结果表明,脑脊液t-tau更能代表突触变性,而非轴突/神经元变性。