Teipel Stefan J, Alexander Gene E, Schapiro Marc B, Möller Hans-Jürgen, Rapoport Stanley I, Hampel Harald
Alzheimer Memorial Center and Geriatric Psychiatry Branch, Dementia and Neuroimaging Section, Department of Psychiatry, Ludwig-Maximilian University, Nussbaumstrasse 7, 80336 Munich, Germany.
Brain. 2004 Apr;127(Pt 4):811-24. doi: 10.1093/brain/awh101. Epub 2004 Feb 25.
Ageing in Down's syndrome is accompanied by amyloid and neurofibrillary pathology the distribution of which replicates pathological features of Alzheimer's disease. With advancing age, an increasing proportion of Down's syndrome subjects >40 years old develop progressive cognitive impairment, resembling the cognitive profile of Alzheimer's disease. Based on these findings, Down's syndrome has been proposed as a model to study the predementia stages of Alzheimer's disease. Using an interactive anatomical segmentation technique and volume-of-interest measurements of MRI, we showed recently that non-demented Down's syndrome adults had significantly reduced hippocampus, entorhinal cortex and corpus callosum sizes with increasing age. In this study, we applied the automated and objective technique of voxel-based morphometry, implemented in SPM99, to the analysis of structural MRI from 27 non-demented Down's syndrome adults (mean age 41.1 years, 15 female). Regional grey matter volume was decreased with advancing age in bilateral parietal cortex (mainly the precuneus and inferior parietal lobule), bilateral frontal cortex with left side predominance (mainly middle frontal gyrus), left occipital cortex (mainly lingual cortex), right precentral and left postcentral gyrus, left transverse temporal gyrus, and right parahippocampal gyrus. The reductions were unrelated to gender, intracranial volume or general cognitive function. Grey matter volume was relatively preserved in subcortical nuclei, periventricular regions, the basal surface of the brain (bilateral orbitofrontal and anterior temporal) and the anterior cingulate gyrus. Our findings suggest grey matter reductions in allocortex and association neocortex in the predementia stage of Down's syndrome. The most likely substrate of these changes is alterations or loss of allocortical and neocortical neurons due to Alzheimer's disease-type pathology.
唐氏综合征患者的衰老伴随着淀粉样蛋白和神经原纤维病变,其分布复制了阿尔茨海默病的病理特征。随着年龄增长,40岁以上的唐氏综合征患者中,越来越多的人出现进行性认知障碍,类似于阿尔茨海默病的认知特征。基于这些发现,唐氏综合征被提议作为研究阿尔茨海默病痴呆前期阶段的模型。我们最近使用交互式解剖分割技术和磁共振成像(MRI)的感兴趣区测量方法,发现未患痴呆的唐氏综合征成年患者,随着年龄增长,海马体、内嗅皮质和胼胝体大小显著减小。在本研究中,我们将在SPM99中实现的基于体素的形态测量自动化客观技术,应用于对27名未患痴呆的唐氏综合征成年患者(平均年龄41.1岁,15名女性)的结构MRI分析。随着年龄增长,双侧顶叶皮质(主要是楔前叶和顶下小叶)、左侧占优势的双侧额叶皮质(主要是额中回)、左侧枕叶皮质(主要是舌回)、右侧中央前回和左侧中央后回、左侧颞横回以及右侧海马旁回的区域灰质体积减小。这些减小与性别、颅内体积或一般认知功能无关。皮质下核团、脑室周围区域、脑基底面(双侧眶额和颞前)以及前扣带回的灰质体积相对保留。我们的研究结果表明,唐氏综合征痴呆前期阶段的异皮质和联合新皮质存在灰质减少。这些变化最可能的基础是由于阿尔茨海默病型病理导致的异皮质和新皮质神经元的改变或丧失。