脑脊液
微泡
生物标志物
医学
一致性
阶段(地层学)
内科学
τ蛋白
外周血
肿瘤科
疾病
病理
阿尔茨海默病
小RNA
生物
古生物学
基因
生物化学
作者
Longfei Jia,Qiongqiong Qiu,Heng Zhang,Lan Chu,Yifeng Du,Jiewen Zhang,Chunkui Zhou,Furu Liang,Shengliang Shi,Shan Wang,Wei Qin,Qi Wang,Fangyu Li,Qigeng Wang,Yan Li,Luxi Shen,Yiping Wei,Jianping Jia
标识
DOI:10.1016/j.jalz.2019.05.002
摘要
Abstract Introduction Neuronal‐derived exosomal Aβ42, T‐tau, and P‐T181‐tau have been demonstrated to be biomarkers of Alzheimer's disease (AD). However, no study has assessed the association of Aβ42, T‐tau, and P‐T181‐tau between exosomes and CSF. Methods This was a multicenter study with two‐stage design. The subjects included 28 AD patients, 25 aMCI patients, and 29 controls in the discovery stage; the results of which were confirmed in the validation stage (73 AD, 71 aMCI, and 72 controls). Results The exosomal concentrations of Aβ42, T‐tau, and P‐T181‐tau in AD group were higher than those in aMCI and control groups (all P < .001). The level of each exosomal biomarker was highly correlated with that in CSF. Discussion This study verified the agreement between CSF and blood exosomal biomarkers and confirmed that exosomal Aβ42, T‐tau, and P‐T181‐tau have the same capacity as those in CSF for the diagnosis of AD and aMCI.
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