Jagust William J, Zheng Ling, Harvey Danielle J, Mack Wendy J, Vinters Harry V, Weiner Michael W, Ellis William G, Zarow Chris, Mungas Dan, Reed Bruce R, Kramer Joel H, Schuff Norbert, DeCarli Charles, Chui Helena C
School of Public Health and Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720-3190, USA.
Ann Neurol. 2008 Jan;63(1):72-80. doi: 10.1002/ana.21296.
Magnetic resonance (MR) imaging is used widely for assessment of patients with cognitive impairment, but the pathological correlates are unclear, especially when multiple pathologies are present.
This report includes 93 subjects from a longitudinally followed cohort recruited for the study of Alzheimer's disease (AD) and subcortical cerebrovascular disease (CVD). MR images were analyzed to quantify cortical gray matter volume, hippocampal volume, white matter hyperintensities, and lacunes. Neuropathological examination quantified CVD parenchymal pathology, AD pathology (defined as Consortium to Establish a Registry for Alzheimer's Disease scores and Braak and Braak stage), and hippocampal sclerosis. Subjects were pathologically classified as 12 healthy control subjects, 46 AD, 14 CVD, 9 mixed AD/CVD, and 12 cognitively impaired patients without significant AD/CVD pathology. Multivariate models tested associations between magnetic resonance and pathological findings across the entire sample.
Pathological correlates of cortical gray matter volume were AD, subcortical vascular pathology, and arteriosclerosis. Hippocampal volume was related to AD pathology and hippocampal sclerosis, and the effects of hippocampal sclerosis were greater for subjects with low levels of AD pathology. White matter hyperintensities were related to age and to white matter pathology. Number of MRI lacunes was related to subcortical vascular pathology.
In this clinical setting, the presence of lacunes and white matter changes provide a good signal for vascular disease. The neuropathological basis of MR defined cerebral cortical and hippocampal atrophy in aging and dementia is complex, with several pathological processes converging on similar brain structures that mediate cognitive decline.
磁共振(MR)成像被广泛用于评估认知障碍患者,但病理相关性尚不清楚,尤其是存在多种病理情况时。
本报告纳入了93名来自纵向随访队列的受试者,该队列是为研究阿尔茨海默病(AD)和皮质下脑血管疾病(CVD)而招募的。对MR图像进行分析,以量化皮质灰质体积、海马体积、白质高信号和腔隙。神经病理学检查量化了CVD实质病变、AD病变(定义为阿尔茨海默病注册协会评分以及Braak和Braak分期)和海马硬化。受试者在病理上被分类为12名健康对照者、46名AD患者、14名CVD患者、9名AD/CVD混合型患者以及12名无明显AD/CVD病理的认知障碍患者。多变量模型测试了整个样本中磁共振与病理结果之间的关联。
皮质灰质体积的病理相关性为AD、皮质下血管病变和动脉硬化。海马体积与AD病变和海马硬化有关,对于AD病变水平较低的受试者,海马硬化的影响更大。白质高信号与年龄和白质病变有关。MRI腔隙数量与皮质下血管病变有关。
在这种临床情况下,腔隙和白质改变的存在为血管疾病提供了一个良好的信号。MR定义的衰老和痴呆中脑皮质和海马萎缩的神经病理学基础很复杂,有几种病理过程汇聚在介导认知衰退的相似脑结构上。