Division of Geriatrics, University of Sao Paulo Medical School, Sao Paulo 01246-903, Brazil.
Department of Pathology, University of São Paulo Medical School, Sao Paulo, SP 01246-903, Brazil; Memory and Aging Center, Weill Institute for Neurosciences, Dept. of Neurology, University of California San Francisco, CA 94158, USA.
Neurobiol Aging. 2025 Jan;145:84-95. doi: 10.1016/j.neurobiolaging.2024.11.001. Epub 2024 Nov 7.
Hypertension, a major modifiable risk factor for cardiovascular diseases, is linked to late-life neurocognitive disorders such as vascular dementia and Alzheimer's disease (AD). This study explores the associations between hypertension, intracranial atherosclerotic disease (ICAD), cerebral small vessel disease (cSVD), and Alzheimer's disease neuropathologic change (ADNC) in a large community-based autopsy study. This cross-sectional study used data from the Biobank for Aging Studies of the University of São Paulo Medical School. Sociodemographic and clinical information was gathered from a reliable next-of-kin informant. Neurofibrillary tangles, neuritic plaques, lacunar infarcts, hyaline arteriolosclerosis, and cerebral amyloid angiopathy were evaluated. Causal mediation analyses with natural effect models were performed to examine indirect associations of hypertension with cerebrovascular pathologies and ADNC through morphometric measurements of intracranial artery lumen obstruction. Hypertensive participants (n = 354) presented a higher rate of stenosed arteries (obstruction ≥ 50 %), critically stenosed arteries (obstruction ≥ 70 %), and more severe ICAD, shown by higher maximum and mean obstruction indexes compared to nonhypertensive participants (n = 166). These measurements of atherosclerosis were associated with neurofibrillary tangles and cSVD lesions. Hypertension was indirectly associated with hyaline arteriolosclerosis and lacunar infarcts through the pathway of ICAD. Presenting hypertension indirectly increased the odds of displaying hyaline arteriolosclerosis by 26 % (95 % CI: 1.08, 1.45, p = 0.002) and lacunar infarcts by 17 % (95 % CI: 1.01, 1.35, p = 0.029). Cognitive and APOE ε4 carrier status did not alter the investigated associations. In this community sample, hypertension was indirectly associated with cSVD through ICAD.
高血压是心血管疾病的一个主要可改变风险因素,与血管性痴呆和阿尔茨海默病(AD)等老年期神经认知障碍有关。本研究通过一项大型社区尸检研究探讨了高血压、颅内动脉粥样硬化性疾病(ICAD)、脑小血管病(cSVD)和阿尔茨海默病神经病理改变(ADNC)之间的关联。本横断面研究使用了来自圣保罗大学医学院生物银行衰老研究的数据。社会人口统计学和临床信息由可靠的近亲信息提供者收集。评估了神经原纤维缠结、神经原纤维斑块、腔隙性梗死、玻璃样小动脉病和脑淀粉样血管病。通过颅内动脉管腔阻塞的形态测量,进行了因果中介分析和自然效应模型,以检查高血压通过颅内动脉狭窄程度与脑小血管病和 ADNC 之间的间接关联。与非高血压参与者(n=166)相比,高血压参与者(n=354)表现出更高的狭窄动脉(阻塞≥50%)、严重狭窄动脉(阻塞≥70%)和更严重的 ICAD,其最大和平均阻塞指数更高。这些动脉粥样硬化的测量值与神经原纤维缠结和 cSVD 病变有关。高血压通过 ICAD 途径与玻璃样小动脉病和腔隙性梗死间接相关。高血压的存在通过 ICAD 使发生玻璃样小动脉病的几率间接增加了 26%(95%CI:1.08,1.45,p=0.002),腔隙性梗死的几率增加了 17%(95%CI:1.01,1.35,p=0.029)。认知和 APOE ε4 携带者状态并没有改变所研究的关联。在这个社区样本中,高血压通过 ICAD 与 cSVD 间接相关。