Liu Ying, Song Jing-Hui, Xu Wei, Hou Xiao-He, Li Jie-Qiong, Yu Jin-Tai, Tan Lan, Chi Song
Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Front Neurosci. 2021 Mar 3;15:633576. doi: 10.3389/fnins.2021.633576. eCollection 2021.
Sex-related difference in Alzheimer's disease (AD) has been proposed, and apolipoprotein E (ApoE) isoforms have been suggested to be involved in the pathogenesis of AD.
We aimed to explore whether cerebrospinal fluid (CSF) ApoE is associated with AD biomarkers and whether the associations are different (between sexes).
Data of 309 participants [92 with normal cognition, 148 with mild cognitive impairment (MCI), and 69 with AD dementia] from the Alzheimer's Disease Neuroimaging Initiative (ADNI) were cross-sectionally evaluated with the multiple linear regression model and longitudinally with the multivariate linear mixed-effects model for the associations of CSF ApoE with AD biomarkers. Sex-ApoE interaction was used to estimate whether sex moderates the associations of CSF ApoE and AD biomarkers.
Significant interactions between CSF ApoE and sex on AD biomarkers were observed [amyloid-β (Aβ): = 0.0169 and phosphorylated-tau (p-tau): = 0.0453]. In women, baseline CSF ApoE levels were significantly associated with baseline Aβ ( = 0.0135) and total-tau (t-tau) ( < 0.0001) as well as longitudinal changes of the biomarkers (Aβ: = 0.0104; t-tau: = 0.0110). In men, baseline CSF ApoE levels were only correlated with baseline p-tau ( < 0.0001) and t-tau ( < 0.0001) and did not aggravate AD biomarkers longitudinally.
The associations between CSF ApoE and AD biomarkers were sex-specific. Elevated CSF ApoE was associated with longitudinal changes of AD biomarkers in women, which indicates that CSF ApoE might be involved in the pathogenesis of AD pathology in a sex-specific way.
已有研究提出阿尔茨海默病(AD)存在性别差异,且载脂蛋白E(ApoE)异构体被认为参与了AD的发病机制。
我们旨在探讨脑脊液(CSF)ApoE是否与AD生物标志物相关,以及这种相关性在性别之间是否存在差异。
对来自阿尔茨海默病神经影像倡议(ADNI)的309名参与者[92名认知正常者、148名轻度认知障碍(MCI)者和69名AD痴呆患者]的数据进行横断面评估,采用多元线性回归模型;纵向评估则采用多变量线性混合效应模型,以研究CSF ApoE与AD生物标志物之间的关联。使用性别 - ApoE交互作用来评估性别是否会调节CSF ApoE与AD生物标志物之间的关联。
观察到CSF ApoE与性别在AD生物标志物上存在显著交互作用[淀粉样蛋白β(Aβ): = 0.0169;磷酸化tau蛋白(p - tau): = 0.0453]。在女性中,基线CSF ApoE水平与基线Aβ( = 0.0135)、总tau蛋白(t - tau)( < 0.0001)以及生物标志物的纵向变化显著相关(Aβ: = 0.0104;t - tau: = 0.0110)。在男性中,基线CSF ApoE水平仅与基线p - tau( < 0.0001)和t - tau( < 0.0001)相关,且在纵向并未加重AD生物标志物的变化。
CSF ApoE与AD生物标志物之间的关联具有性别特异性。CSF ApoE升高与女性AD生物标志物的纵向变化相关,这表明CSF ApoE可能以性别特异性方式参与AD病理的发病机制。