Hajjar Ihab, Brown Lauren, Mack Wendy J, Chui Helena
Arch Neurol. 2012 Dec;69(12):1632-8. doi: 10.1001/archneurol.2012.1010.
BACKGROUND Angiotensin II may be involved in amyloid metabolism in the brain. Angiotensin receptor blockers (ARBs) may also prevent cognitive decline. OBJECTIVE To evaluate the impact of treatment with ARBs on the neuropathology of Alzheimer disease (AD) in the National Alzheimer Coordinating Center database, which includes aggregated data and brain autopsies from 29 AD centers throughout the United States. DESIGN Multiple logistic regression was used to compare the pathologic findings in hypertensive subjects taking ARBs with those taking other antihypertensive treatments as well as with hypertensive subjects who did not receive antihypertensive medications. SETTING Neuropathologic data included neuritic plaque and neurofibrillary tangle measures and vascular injury markers. PATIENTS Data were collected from participants who were self-referred or provider-referred and included those with and without cognitive disorders. Our sample included only hypertensive participants and excluded cognitively and neuropathologically normal participants (N = 890; mean age at death, 81 years [range, 39-107 years]; 43% women; 94% white). RESULTS Participants with or without AD who were treated with ARBs showed less amyloid deposition markers compared with those treated with other antihypertensive medications (lower Consortium to Establish a Registry of Alzheimer Disease score: odds ratio, 0.47, 95% CI, 0.27-0.81; Alzheimer Disease and Related Disorders Association score: odds ratio, 0.43, 95% CI, 0.21-0.91; Braak and Braak stage: odds ratio, 0.52, 95% CI, 0.31-0.85; neuritic plaques: odds ratio, 0.59, 95% CI, 0.37-0.96). They also had less AD-related pathology compared with untreated hypertensive subjects. Participants who received ARBs were more likely to have had a stroke; hence, they had more frequent pathologic evidence of large vessel infarct and hemorrhage. CONCLUSION Treatment with ARBs is associated with less AD-related pathology on autopsy evaluations. The effect of ARBs on cognitive decline in those with dementia or AD needs further investigation.
背景 血管紧张素II可能参与大脑中的淀粉样蛋白代谢。血管紧张素受体阻滞剂(ARB)也可能预防认知能力下降。目的 在国家阿尔茨海默病协调中心数据库中评估ARB治疗对阿尔茨海默病(AD)神经病理学的影响,该数据库包含来自美国29个AD中心的汇总数据和脑尸检结果。设计 采用多因素logistic回归比较服用ARB的高血压患者与服用其他抗高血压药物的患者以及未接受抗高血压药物治疗的高血压患者的病理结果。单位 神经病理学数据包括神经炎性斑块和神经原纤维缠结测量以及血管损伤标志物。患者 数据收集自自我推荐或由医疗服务提供者推荐的参与者,包括有和没有认知障碍的参与者。我们的样本仅包括高血压参与者,排除了认知和神经病理学正常的参与者(N = 890;死亡时的平均年龄为81岁[范围39 - 107岁];43%为女性;94%为白人)。结果 与接受其他抗高血压药物治疗的参与者相比,接受ARB治疗的有或没有AD的参与者显示出较少的淀粉样蛋白沉积标志物(较低的阿尔茨海默病注册协会评分:比值比,0.47,95%可信区间,0.27 - 0.81;阿尔茨海默病及相关疾病协会评分:比值比,0.43,95%可信区间,0.21 - 0.91;Braak和Braak分期:比值比,0.52,95%可信区间,0.31 - 0.85;神经炎性斑块:比值比,0.59,95%可信区间,0.37 - 0.96)。与未治疗的高血压患者相比,他们的AD相关病理学也较少。接受ARB治疗的参与者更有可能发生过中风;因此,他们有更频繁的大血管梗死和出血的病理证据。结论 在尸检评估中,ARB治疗与较少的AD相关病理学有关。ARB对痴呆或AD患者认知能力下降的影响需要进一步研究。