Department of Pathology and Laboratory Medicine, Institute on Ageing, Centre for Neurodegenerative Disease Research, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Brain. 2013 Sep;136(Pt 9):2697-706. doi: 10.1093/brain/awt188. Epub 2013 Jul 10.
Cerebrovascular disease and vascular risk factors are associated with Alzheimer's disease, but the evidence for their association with other neurodegenerative disorders is limited. Therefore, we compared the prevalence of cerebrovascular disease, vascular pathology and vascular risk factors in a wide range of neurodegenerative diseases and correlate them with dementia severity. Presence of cerebrovascular disease, vascular pathology and vascular risk factors was studied in 5715 cases of the National Alzheimer's Coordinating Centre database with a single neurodegenerative disease diagnosis (Alzheimer's disease, frontotemporal lobar degeneration due to tau, and TAR DNA-binding protein 43 immunoreactive deposits, α-synucleinopathies, hippocampal sclerosis and prion disease) based on a neuropathological examination with or without cerebrovascular disease, defined neuropathologically. In addition, 210 'unremarkable brain' cases without cognitive impairment, and 280 cases with pure cerebrovascular disease were included for comparison. Cases with cerebrovascular disease were older than those without cerebrovascular disease in all the groups except for those with hippocampal sclerosis. After controlling for age and gender as fixed effects and centre as a random effect, we observed that α-synucleinopathies, frontotemporal lobar degeneration due to tau and TAR DNA-binding protein 43, and prion disease showed a lower prevalence of coincident cerebrovascular disease than patients with Alzheimer's disease, and this was more significant in younger subjects. When cerebrovascular disease was also present, patients with Alzheimer's disease and patients with α-synucleinopathy showed relatively lower burdens of their respective lesions than those without cerebrovascular disease in the context of comparable severity of dementia at time of death. Concurrent cerebrovascular disease is a common neuropathological finding in aged subjects with dementia, is more common in Alzheimer's disease than in other neurodegenerative disorders, especially in younger subjects, and lowers the threshold for dementia due to Alzheimer's disease and α-synucleinopathies, which suggests that these disorders should be targeted by treatments for cerebrovascular disease.
脑血管疾病和血管危险因素与阿尔茨海默病有关,但它们与其他神经退行性疾病的关联证据有限。因此,我们比较了广泛的神经退行性疾病中脑血管疾病、血管病理学和血管危险因素的患病率,并将其与痴呆严重程度相关联。根据有无脑血管疾病的神经病理学检查,对美国国家阿尔茨海默病协调中心数据库中的 5715 例单一神经退行性疾病诊断病例(阿尔茨海默病、tau 引起的额颞叶变性、TAR DNA 结合蛋白 43 免疫反应性沉积物、α-突触核蛋白病、海马硬化和朊病毒病)进行了脑血管疾病、血管病理学和血管危险因素的研究。此外,还纳入了 210 例无认知障碍的“正常脑”病例和 280 例单纯脑血管疾病病例作为对照。除了海马硬化组外,所有组中伴有脑血管疾病的病例均比不伴有脑血管疾病的病例年龄更大。在控制了年龄和性别作为固定效应以及中心作为随机效应后,我们观察到α-突触核蛋白病、tau 引起的额颞叶变性和 TAR DNA 结合蛋白 43、朊病毒病的并发脑血管疾病的患病率低于阿尔茨海默病患者,且在年轻患者中更为显著。当同时存在脑血管疾病时,与无脑血管疾病的患者相比,阿尔茨海默病患者和α-突触核蛋白病患者在死亡时痴呆严重程度相当时,其各自病变的负担相对较低。并发脑血管疾病是老年痴呆患者常见的神经病理学发现,在阿尔茨海默病中比在其他神经退行性疾病中更为常见,尤其是在年轻患者中,这降低了阿尔茨海默病和α-突触核蛋白病引起的痴呆的阈值,这表明这些疾病应该成为脑血管疾病治疗的靶点。