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在无痴呆症的老年人中,较高的血浆载脂蛋白C-III与脑脊液中β-淀粉样蛋白水平降低较慢有关。

Higher Plasma APOC-III Was Associated with a Slower Reduction of β-Amyloid Levels in Cerebrospinal Fluid Among Older Individuals Without Dementia.

作者信息

Zhang Xiaoyan

机构信息

Department of Child Healthcare, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, People's Republic of China.

出版信息

Neuropsychiatr Dis Treat. 2020 May 5;16:1139-1144. doi: 10.2147/NDT.S238985. eCollection 2020.

Abstract

PURPOSE

Although emerging evidence has suggested that apolipoprotein C-III (APOC-III) is involved in the pathogenesis of Alzheimer's disease (AD), the association of APOC-III with longitudinal changes in cerebrospinal fluid (CSF) AD pathologies (β-amyloid (Aβ42) and tau proteins) is not clear. In the present study, we aimed to examine whether plasma APOC-III levels are associated with longitudinal changes in CSF Aβ42, total-tau (t-tau), and phosphorylated-tau (p-tau) levels among older individuals without dementia.

PATIENTS AND METHODS

Linear mixed models were fitted with plasma APOC-III used as a predictor for longitudinal changes in CSF AD biomarkers over a 7-year period. Data were obtained from the Alzheimer's Disease Neuroimaging Initiative database, and 195 older individuals without dementia (47 subjects with normal cognition (NC) and 148 subjects with mild cognitive impairment (MCI)) with baseline plasma APOC-III measurements were included.

RESULTS

Among older individuals without dementia, we found that the tertiles of plasma APOC-III were associated with changes in CSF Aβ42, but not t-tau or p-tau. Specifically, the CSF Aβ42 reduction for individuals in the highest plasma APOC-III tertile was significantly slower compared with those in the middle tertile, whereas no other pairwise difference was found to be statistically significant.

CONCLUSION

Among older individuals without dementia, higher plasma APOC-III levels were associated with slower declines in CSF Aβ42.

摘要

目的

尽管新出现的证据表明载脂蛋白C-III(APOC-III)参与了阿尔茨海默病(AD)的发病机制,但APOC-III与脑脊液(CSF)中AD病理标志物(β-淀粉样蛋白(Aβ42)和tau蛋白)的纵向变化之间的关联尚不清楚。在本研究中,我们旨在探讨在无痴呆的老年人中,血浆APOC-III水平是否与脑脊液Aβ42、总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)水平的纵向变化相关。

患者与方法

采用线性混合模型,将血浆APOC-III作为预测因子,用于预测7年期间脑脊液AD生物标志物的纵向变化。数据来自阿尔茨海默病神经影像学倡议数据库,纳入了195名无痴呆的老年人(47名认知正常(NC)受试者和148名轻度认知障碍(MCI)受试者),这些受试者均有基线血浆APOC-III测量值。

结果

在无痴呆的老年人中,我们发现血浆APOC-III的三分位数与脑脊液Aβ42的变化相关,但与t-tau或p-tau无关。具体而言,血浆APOC-III三分位数最高的个体脑脊液Aβ42的降低明显慢于中间三分位数的个体,而其他两两比较差异均无统计学意义。

结论

在无痴呆的老年人中,较高的血浆APOC-III水平与脑脊液Aβ42下降较慢有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539a/7213010/53284232f734/NDT-16-1139-g0001.jpg

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