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当代阿耳茨海默病研究

Editor-in-Chief

ISSN (Print): 1567-2050
ISSN (Online): 1875-5828

Research Article

脑脊液生物标志物水平作为阿尔茨海默病疗养院安置和存活时间的标志物

卷 18, 期 7, 2021

发表于: 22 October, 2021

页: [573 - 584] 页: 12

弟呕挨: 10.2174/1567205018666211022164952

open access plus

摘要

背景:脑脊液 (CSF) 生物标志物与轻度认知障碍向阿尔茨海默病 (AD) 的转变有关,但它们对后期终点的预测价值的评估较少,结果不一致。 目的:我们研究了 CSF 淀粉样蛋白-β1-42 (Aβ42)、磷酸化 tau (P-tau) 和总 tau (T-tau) 与养老院安置 (NHP) 时间和诊断后预期寿命之间的潜在关系。 方法:这项前瞻性观察研究包括 129 名临床诊断为轻度至中度 AD 并接受腰椎穿刺的门诊患者。使用 xMAP 技术分析 CSF 生物标志物。记录住院和死亡日期。 结果:经过 20 年的随访,123 名患者(95%)死亡。具有异常 P-tau 和 T-tau (A+ T+ (N)+) 的参与者比具有正常 P-tau/异常 T-tau (A+ T- (N)+) 的参与者更早死亡(平均,80.5 岁 vs. 85.4 岁)。在较低的 Aβ42 和较短的 NHP 时间(p = 0.017)以及较高的 P-tau 和较年轻的死亡年龄(p = 0.016)之间证明了线性关联。 AD 诊断后的存活率与 CSF 生物标志物之间未检测到相关性。在性别和年龄调整的 Cox 回归模型中,较高的 P-tau 和 T-tau 是诊断后寿命较短的独立预测因子。在多变量 Cox 模型中,年龄较大和基线认知状态较低,但 tau 不升高,显着促进了收容和死亡。 结论:这些发现表明 CSF 生物标志物水平在 AD 的痴呆阶段趋于稳定,这可能会限制其与临床终点(如 NHP 和生存时间)的可能关系。然而,生物标志物反映了 AD 的主要病理生理学。特别是,病理性 tau 与更晚期的疾病、更年轻的发病年龄和更早的死亡有关。

关键词: 阿尔茨海默病、疗养院安置、死亡率、纵向研究、预测因子、脑脊液生物标志物、AT(N)、Tau。

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