Teipel Stefan J, Hampel Harald
Alzheimer Memorial Center and Geriatric Psychiatry Branch, Dementia and Neuroimaging Section, Department of Psychiatry, Ludwig-Maximilian University, Munich, Germany.
Behav Genet. 2006 May;36(3):405-15. doi: 10.1007/s10519-006-9047-x. Epub 2006 Feb 17.
Aging in Down syndrome (DS) is accompanied by neuropathological features of Alzheimer's disease (AD). Therefore, DS has been proposed as a model to study predementia stages of AD. MRI-based measurement of grey matter atrophy is an in vivo surrogate marker of regional neuronal density. A range of neuroimaging studies have described the macroscopic neuroanatomy of DS. Recent studies using sensitive quantitative measures of region-specific atrophy based on high-resolution MRI suggest that age-related atrophy in DS resembles the pattern of brain atrophy in early stages of AD. The pattern of atrophy determined in predementia DS supports the notion that AD-type pathology leads to neuronal degeneration not only in allocortical, but also in neocortical brain areas before onset of clinical dementia. This has major implications for our understanding of the onset and progression of AD-type pathology both in DS and in sporadic AD.
唐氏综合征(DS)患者的衰老伴有阿尔茨海默病(AD)的神经病理学特征。因此,DS已被提议作为研究AD痴呆前期阶段的模型。基于MRI的灰质萎缩测量是区域神经元密度的一种体内替代标志物。一系列神经影像学研究描述了DS的宏观神经解剖结构。最近基于高分辨率MRI对区域特异性萎缩进行敏感定量测量的研究表明,DS中与年龄相关的萎缩类似于AD早期阶段的脑萎缩模式。在痴呆前期DS中确定的萎缩模式支持了这样一种观点,即AD型病理不仅导致异皮质,而且在临床痴呆发作前也导致新皮质脑区的神经元变性。这对于我们理解DS和散发性AD中AD型病理的发生和进展具有重要意义。