载脂蛋白E
脑脊液
阿尔茨海默病神经影像学倡议
神经炎症
调解
内科学
生物标志物
心理学
疾病
神经影像学
医学
肿瘤科
痴呆
病理
神经科学
生物
生物化学
政治学
法学
作者
Yujing Lin,Ying Liu,Ze-Hu Sheng,Yan Fu,Lingzhi Ma,Zi-Hao Zhang,Lan-Yang Wang,Lin Huang,Min Liu,Zuo-Teng Wang,Lan Tan
标识
DOI:10.1177/13872877251320419
摘要
Background The roles of complement 1q (C1q) and Apolipoprotein E (ApoE) in driving Alzheimer's disease (AD) progression might be explained by their associations with neuroinflammation and AD pathology which were previously reported. Objective We examined the associations of cerebrospinal fluid (CSF) C1q and ApoE with CSF neuroinflammatory biomarkers and AD core biomarkers, as well as explored whether C1q mediated the associations of CSF ApoE with these biomarkers. Methods Here, we analyzed CSF proteomics data from Alzheimer's Disease Neuroimaging Initiative (ADNI) using two different ADNI proteomics datasets—SomaScan (n = 579)and multiple reaction monitoring (MRM[n = 207]). Linear regression analyses were conducted to explore the association of CSF ApoE and C1q. The mediation model and structural equation model (SEM) were conducted to explore the associations of ApoE and C1q with AD biomarkers. Results Multiple linear regression showed that CSF ApoE was positively associated with CSF C1q in total participants and Alzheimer's continuum participants. Mediation analyses indicated that C1q mediated the associations of CSF ApoE with CSF T-tau, P-tau, sTREM2 and GFAP (mediation proportions range from 15.06 to 44.64%; all the p values < 0.05) but not with CSF amyloid-β and progranulin (PGRN). The SEM yielded similar results. Conclusions Our findings suggest that C1q is linked to ApoE, and it mediates the associations of ApoE with T-tau, P-tau, sTREM2, GFAP, indicating C1q association with ApoE might be involved in AD progression.
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