Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Department of Anesthesiology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Ann Clin Transl Neurol. 2020 Oct;7(10):1766-1778. doi: 10.1002/acn3.51153. Epub 2020 Sep 10.
To examine whether apolipoprotein B (ApoB), apolipoprotein A-1 (ApoA1), or their ratio (ApoB/A1) were associated with early changes in cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) pathology in elderly adults with subjective cognitive decline (SCD).
This study included 507 objective cognitive normal participants from the Chinese Alzheimer's Biomarker and LifestylE (CABLE) database including 288 cognitive normal participants (CN) and 219 SCD. Multiple linear regression models were used to examine the associations of apolipoproteins with CSF AD biomarkers.
Compared with control group, SCD participants with significant AD biological characteristics had lower ApoB levels (P = 0.0461). In total participants, lower level of serum ApoB was associated with decreases in CSF Aβ42 (P = 0.0015) and Aβ42/40 (P = 0.0081) as well as increases in CSF p-tau/Aβ42 (P < 0.0001) and t-tau/Aβ42 (P = 0.0013), independent of APOEɛ4 status. In further subgroup analysis, these associations were more significant in SCD participants (ApoB × Diagnose: P < 0.05). In addition, lower levels of ApoB were also found associated with increases in p-tau in the SCD subgroup (P = 0.0263). Furthermore, these protective associations were more significant in the overweight participants (ApoB × weight: P < 0.05). Results showed no association between ApoA1 and CSF biomarkers.
This study is the first to find protective associations of serum ApoB with CSF AD core biomarkers, especially in SCD individuals. It indicated that ApoB may be a potential biomarker for preclinical AD and may play different roles in different stages of AD.
探讨载脂蛋白 B(ApoB)、载脂蛋白 A-1(ApoA1)或其比值(ApoB/A1)与伴有主观认知下降(SCD)的老年人群中阿尔茨海默病(AD)病理的脑脊液(CSF)生物标志物早期变化是否相关。
本研究纳入了来自中国阿尔茨海默病生物标志物和生活方式(CABLE)数据库的 507 名客观认知正常的参与者,其中包括 288 名认知正常参与者(CN)和 219 名 SCD。采用多元线性回归模型来检验载脂蛋白与 CSF AD 生物标志物的相关性。
与对照组相比,具有显著 AD 生物学特征的 SCD 参与者的 ApoB 水平较低(P=0.0461)。在所有参与者中,血清 ApoB 水平较低与 CSF Aβ42(P=0.0015)和 Aβ42/40(P=0.0081)降低以及 CSF p-tau/Aβ42(P<0.0001)和 t-tau/Aβ42(P=0.0013)升高有关,且独立于 APOEɛ4 状态。在进一步的亚组分析中,这些相关性在 SCD 参与者中更为显著(ApoB×诊断:P<0.05)。此外,在 SCD 亚组中还发现 ApoB 水平较低与 p-tau 升高有关(P=0.0263)。此外,在超重参与者中,这些保护相关性更为显著(ApoB×体重:P<0.05)。结果未发现 ApoA1 与 CSF 生物标志物之间存在关联。
本研究首次发现血清 ApoB 与 CSF AD 核心生物标志物之间存在保护性关联,尤其是在 SCD 个体中。这表明 ApoB 可能是 AD 临床前的一个潜在生物标志物,并且在 AD 的不同阶段可能发挥不同的作用。