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服用血管紧张素Ⅱ1型受体阻滞剂的老年人脑淀粉样蛋白潴留减少。

Older Adults Taking AT1-Receptor Blockers Exhibit Reduced Cerebral Amyloid Retention.

作者信息

Nation Daniel A, Ho Jean, Yew Belinda

出版信息

J Alzheimers Dis. 2016;50(3):779-89. doi: 10.3233/JAD-150487.

Abstract

BACKGROUND

Evidence suggests that angiotensin II AT1-receptor blockers (ARBs) may be protective against dementia, and studies in transgenic animals indicate that this may be due to improved amyloid-β (Aβ) clearance.

OBJECTIVE

We investigated whether taking ARBs was associated with an attenuation of age-related increases in cerebral Aβ retention, and reduced progression to dementia.

METHODS

Eight hundred seventy-one stroke-free and dementia-free older adults from the Alzheimer's Disease Neuroimaging Initiative (ADNI) study underwent baseline lumbar puncture, and a subgroup (n = 124) underwent 12 and 24 month follow-up lumbar puncture. Participants were followed at variable intervals for clinical progression to dementia. Linear mixed models and ANCOVA compared ARBs users with those taking other antihypertensives (O-antiHTN) or no antihypertensives (No-antiHTN) on cerebrospinal fluid (CSF) Aβ and phosphorylated tau (P-tau) levels. Cox regression and chi-square analyses compared groups on progression to dementia.

RESULTS

ARBs users exhibited greater vascular risk and lower educational attainment than the No-antiHTN group. Longitudinal analyses indicated higher CSF Aβ and lower P-tau in ARBs users versus other groups. Cross-sectional analyses revealed age-related decreases in CSF Aβ in other groups but not ARBs users. ARBs users were less likely to progress to dementia and showed reduced rate of progression relative to the No-antiHTN group.

DISCUSSION

Patients taking ARBs showed an attenuation of age-related decreases in CSF Aβ, a finding that is consistent with studies done in transgenic animals. These findings may partly explain why ARBs users show reduced progression to dementia despite their lower educational attainment and greater vascular risk burden.

摘要

背景

有证据表明,血管紧张素II AT1受体阻滞剂(ARB)可能对痴呆具有保护作用,并且在转基因动物中的研究表明,这可能是由于淀粉样β蛋白(Aβ)清除率提高所致。

目的

我们研究了服用ARB是否与脑Aβ潴留的年龄相关性增加的减弱以及痴呆进展的减缓有关。

方法

来自阿尔茨海默病神经影像学倡议(ADNI)研究的871名无中风且无痴呆的老年人接受了基线腰椎穿刺,一个亚组(n = 124)接受了12个月和24个月的随访腰椎穿刺。以不同的时间间隔对参与者进行随访,观察其痴呆的临床进展情况。线性混合模型和协方差分析比较了ARB使用者与服用其他抗高血压药物(O-antiHTN)或未服用抗高血压药物(No-antiHTN)者在脑脊液(CSF)Aβ和磷酸化tau蛋白(P-tau)水平上的差异。Cox回归和卡方分析比较了各组在痴呆进展方面的差异。

结果

与No-antiHTN组相比,ARB使用者表现出更高的血管风险和更低的教育程度。纵向分析表明,与其他组相比,ARB使用者的CSF Aβ水平更高,P-tau水平更低。横断面分析显示,其他组的CSF Aβ随年龄下降,而ARB使用者则不然。ARB使用者进展为痴呆的可能性较小,且相对于No-antiHTN组,其进展速度有所降低。

讨论

服用ARB的患者CSF Aβ与年龄相关的下降有所减弱,这一发现与转基因动物研究结果一致。这些发现可能部分解释了为什么尽管ARB使用者教育程度较低且血管风险负担较重,但他们进展为痴呆的情况较少。

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