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Neuroanatomy of Down syndrome in vivo: a model of preclinical Alzheimer's disease.

机译:唐氏综合症的体内神经解剖学:临床前阿尔茨海默氏病模型。

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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.
机译:唐氏综合症(DS)伴有阿尔茨海默氏病(AD)的神经病理特征。因此,已经提出将DS作为研究AD的痴呆阶段的模型。基于MRI的灰质萎缩症的测量是体内区域神经元密度的替代指标。大量的神经影像研究已经描述了DS的宏观神经解剖学。最近的研究使用基于高分辨率MRI的区域特异性萎缩的敏感定量测量方法,发现DS中与年龄相关的萎缩类似于AD早期脑萎缩的模式。在痴呆前DS中确定的萎缩模式支持以下观念:AD型病理不仅导致分配性痴呆,而且还导致临床痴呆发作前神经皮质变性。这对于我们对DS和散发性AD中AD型病理的发作和进展的理解具有重大意义。

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