Biel Davina, Suárez-Calvet Marc, Dewenter Anna, Steward Anna, Roemer Sebastian N, Dehsarvi Amir, Zhu Zeyu, Pescoller Julia, Frontzkowski Lukas, Kreuzer Annika, Haass Christian, Schöll Michael, Brendel Matthias, Franzmeier Nicolai
Institute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, Munich, Germany.
Barcelonaβeta Brain Research Center (BBRC), Pasqual Maragall Foundation, Barcelona, Spain.
EMBO Mol Med. 2025 Feb;17(2):235-248. doi: 10.1038/s44321-024-00190-3. Epub 2025 Jan 10.
In Alzheimer's disease (AD), Aβ triggers p-tau secretion, which drives tau aggregation. Therefore, it is critical to characterize modulators of Aβ-related p-tau increases which may alter AD trajectories. Here, we assessed whether factors known to alter tau levels in AD modulate the association between fibrillar Aβ and secreted p-tau determined in the cerebrospinal fluid (CSF). To assess potentially modulating effects of female sex, younger age, and ApoE4, we included 322 ADNI participants with cross-sectional/longitudinal p-tau. To determine effects of microglial activation on p-tau, we included 454 subjects with cross-sectional CSF sTREM2. Running ANCOVAs for nominal and linear regressions for metric variables, we found that women had higher Aβ-related p-tau levels. Higher sTREM2 was associated with elevated p-tau, with stronger associations in women. Similarly, ApoE4 was related to higher p-tau levels and faster p-tau increases, with stronger effects in female ApoE4 carriers. Our results show that sex alone modulates the Aβ to p-tau axis, where women show higher Aβ-dependent p-tau secretion, potentially driven by elevated sTREM2-related microglial activation and stronger effects of ApoE4 carriership in women.
在阿尔茨海默病(AD)中,β淀粉样蛋白(Aβ)引发磷酸化tau蛋白(p-tau)分泌,进而促使tau蛋白聚集。因此,明确可能改变AD病程的Aβ相关p-tau增加的调节因子至关重要。在此,我们评估了已知可改变AD中tau蛋白水平的因素是否会调节脑脊液(CSF)中检测到的纤维状Aβ与分泌型p-tau之间的关联。为评估女性性别、年轻年龄和载脂蛋白E4(ApoE4)的潜在调节作用,我们纳入了322名有横断面/纵向p-tau数据的阿尔茨海默病神经影像学计划(ADNI)参与者。为确定小胶质细胞激活对p-tau的影响,我们纳入了454名有横断面CSF中可溶性触发受体表达量2(sTREM2)数据的受试者。通过对名义变量进行协方差分析以及对计量变量进行线性回归分析,我们发现女性的Aβ相关p-tau水平更高。较高的sTREM2与升高的p-tau相关,在女性中关联更强。同样,ApoE4与更高的p-tau水平以及更快的p-tau增加相关,在女性ApoE4携带者中影响更强。我们的结果表明,仅性别就可调节Aβ到p-tau的轴,女性表现出更高的Aβ依赖性p-tau分泌,这可能是由sTREM2相关的小胶质细胞激活增加以及女性中ApoE4携带者的更强效应所驱动。