Department of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD, USA.
Department of Mental Health, Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD, USA.
J Alzheimers Dis. 2020;75(2):521-529. doi: 10.3233/JAD-200118.
There is emerging evidence about possible involvement of the renin-angiotensin system (RAS) in the pathogenesis of Alzheimer's disease (AD) and decline of cognitive function. However, little is known about associations with brain biomarkers.
Our study aimed to examine associations between blood ACE-1 and ANG II levels and brain MRI based volumes in non-demented participants, and whether these associations were mediated by blood pressure.
This cross-sectional study was conducted in 34 older participants from the Baltimore Experience Corps Trial (BECT) Brain Health Sub-study (BHS). Blood ANGII and ACE-1 levels were measured by ELISA and brain MRI volumes were generated using FreeSurfer 6.0. Multiple linear regression analysis, adjusting for intracranial volume and confounders, was used to determine associations between log transformed ANGII and ACE-1 levels and MRI volumes (mm3).
Participants were predominantly female (76%), African-American (94%), with mean age of 66.9 and education of 14.4 years. In the fully adjusted model we observed significant inverse associations between log ANGII levels and total grey matter (β=Angiotensin II associated with smaller hippocampus14,935.50, ±7,444.83, p = 0.05), total hippocampus (β=-129.97, ±105.27, p = 0.03), rostral middle frontal (β= -1580.40, ±584.74, p = 0.02), and supramarginal parietal (β= -978.90, ±365.54, p = 0.02) volumes. There were no associations between ANGII levels and total white matter or entorhinal cortex volumes, or ACE-1 levels and any brain volumes.
We observed that increased blood ANGII levels were associated with lower total grey matter, hippocampal, rostral middle frontal, and supramarginal parietal volumes, which are associated with cognitive domains that decline in preclinical AD.
越来越多的证据表明肾素-血管紧张素系统(RAS)可能参与阿尔茨海默病(AD)的发病机制和认知功能下降。然而,人们对与大脑生物标志物的关联知之甚少。
我们的研究旨在检查非痴呆参与者的血液 ACE-1 和 ANG II 水平与大脑 MRI 基于体积之间的关联,以及这些关联是否由血压介导。
这项横断面研究在巴尔的摩体验军团试验(BECT)大脑健康子研究(BHS)的 34 名老年参与者中进行。通过 ELISA 测量血液 ANGII 和 ACE-1 水平,并使用 FreeSurfer 6.0 生成大脑 MRI 体积。使用多元线性回归分析,调整颅内体积和混杂因素,确定 log 转换 ANGII 和 ACE-1 水平与 MRI 体积(mm3)之间的关联。
参与者主要为女性(76%)、非裔美国人(94%),平均年龄为 66.9 岁,教育程度为 14.4 年。在完全调整的模型中,我们观察到 log ANGII 水平与总灰质(β=与较小的海马体相关的血管紧张素 II14935.50,±7444.83,p=0.05)、总海马体(β=-129.97,±105.27,p=0.03)、额中回(β=-1580.40,±584.74,p=0.02)和缘上回顶叶(β=-978.90,±365.54,p=0.02)体积之间存在显著负相关。ANGII 水平与总白质或内嗅皮质体积之间没有关联,ACE-1 水平与任何大脑体积之间也没有关联。
我们发现,血液 ANGII 水平升高与总灰质、海马体、额中回和缘上回顶叶体积降低有关,这些体积与认知域有关,这些认知域在临床前 AD 中下降。