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雷米普利对阿尔茨海默病高危人群的影响:一项试点临床试验的结果。

The effects of ramipril in individuals at risk for Alzheimer's disease: results of a pilot clinical trial.

机构信息

Alzheimer's Disease Research Center, University of Wisconsin, Madison, WI 53705, USA.

出版信息

J Alzheimers Dis. 2012;32(1):147-56. doi: 10.3233/JAD-2012-120763.

Abstract

Research shows that certain antihypertensives taken during midlife confer Alzheimer's disease (AD) related benefits in later life. We conducted a clinical trial to evaluate the extent to which the angiotensin converting enzyme inhibitor (ACE-I), ramipril, affects AD biomarkers including cerebrospinal fluid (CSF) amyloid-β (Aβ) levels and ACE activity, arterial function, and cognition in participants with a parental history of AD. This four month randomized, double-blind, placebo-controlled, pilot clinical trial evaluated the effects of ramipril, a blood-brain-barrier crossing ACE-I, in cognitively healthy individuals with mild, or Stage I hypertension. Fourteen participants were stratified by gender and apolipoprotein E ε4 (APOE ε4) status and randomized to receive 5 mg of ramipril or matching placebo daily. Participants were assessed at baseline and month 4 on measures of CSF Aβ(1-42) and ACE activity, arterial function, and cognition. Participants were middle-aged (mean 54 y) and highly educated (mean 15.4 y), and included 50% men and 50% APOE ε4 carriers. While results did not show a treatment effect on CSF Aβ(1-42) (p = 0.836), data revealed that ramipril can inhibit CSF ACE activity (p = 0.009) and improve blood pressure, however, there were no differences between groups in arterial function or cognition. In this study, ramipril therapy inhibited CSF ACE activity and improved blood pressure, but did not influence CSF Aβ1-42. While larger trials are needed to confirm our CSF Aβ results, it is possible that prior research reporting benefits of ACE-I during midlife may be attributed to alternative mechanisms including improvements in cerebral blood flow or the prevention of angiotensin II-mediated inhibition of acetylcholine.

摘要

研究表明,中年时期服用某些降压药可在晚年带来与阿尔茨海默病(AD)相关的益处。我们进行了一项临床试验,以评估血管紧张素转换酶抑制剂(ACE-I)雷米普利对具有 AD 家族史的参与者的 AD 生物标志物(包括脑脊液(CSF)中的淀粉样蛋白-β(Aβ)水平和 ACE 活性、动脉功能和认知)的影响。这项为期四个月的随机、双盲、安慰剂对照、初步临床试验评估了一种血脑屏障穿透性 ACE-I 雷米普利在认知健康、轻度或 I 期高血压个体中的作用。根据性别和载脂蛋白 E ε4(APOE ε4)状态对 14 名参与者进行分层,并随机分配每天接受 5 毫克雷米普利或匹配的安慰剂。在基线和第 4 个月时,参与者接受了脑脊液 Aβ(1-42)和 ACE 活性、动脉功能和认知的评估。参与者为中年(平均年龄 54 岁)且受过高等教育(平均受教育年限为 15.4 年),包括 50%的男性和 50%的 APOE ε4 携带者。虽然结果显示雷米普利对 CSF Aβ(1-42)没有治疗作用(p=0.836),但数据显示雷米普利可以抑制 CSF ACE 活性(p=0.009)并改善血压,但组间动脉功能或认知没有差异。在这项研究中,雷米普利治疗抑制了 CSF ACE 活性并改善了血压,但并未影响 CSF Aβ1-42。虽然需要更大的试验来证实我们的 CSF Aβ 结果,但先前报告 ACE-I 在中年时期有益的研究可能归因于其他机制,包括改善脑血流或预防血管紧张素 II 介导的乙酰胆碱抑制。

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