MRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain; Centro Investigación Biomédica en Red de Salud Mental, CIBERSAM G21, 08003 Barcelona, Spain.
MRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain.
Neuroimage Clin. 2018 Jan 28;18:160-166. doi: 10.1016/j.nicl.2018.01.024. eCollection 2018.
We longitudinally assessed Down syndrome individuals at the age of risk of developing dementia to measure changes in brain anatomy and their relationship to cognitive impairment progression.
Forty-two Down syndrome individuals were initially included, of whom 27 (mean age 46.8 years) were evaluable on the basis of completing the 2-year follow-up and success in obtaining good quality MRI exams. Voxel-based morphometry was used to estimate regional brain volumes at baseline and follow-up on 3D anatomical images. Longitudinal volume changes for the group and their relationship with change in general cognitive status and specific cognitive domains were mapped.
As a group, significant volume reduction was identified in the substantia innominata region of the basal forebrain, hippocampus, lateral temporal cortex and left arcuate fasciculus. Volume reduction in the substantia innominata and hippocampus was more prominent in individuals whose clinical status changed from cognitively stable to mild cognitive impairment or dementia during the follow-up. Relevantly, longitudinal memory score change was specifically associated with volume change in the hippocampus, prospective memory with prefrontal lobe and verbal comprehension with language-related brain areas.
Results are notably concordant with the well-established anatomical changes signaling the progression to dementia in Alzheimer's disease, despite the dense baseline pathology that developmentally accumulates in Down syndrome. This commonality supports the potential value of Down syndrome as a genetic model of Alzheimer's neurodegeneration and may serve to further support the view that Down syndrome patients are best candidates to benefit from treatment research in Alzheimer's disease.
我们对处于痴呆风险期的唐氏综合征个体进行了纵向评估,以测量大脑解剖结构的变化及其与认知障碍进展的关系。
最初纳入了 42 名唐氏综合征个体,其中 27 名(平均年龄 46.8 岁)在完成 2 年随访并成功获得高质量 MRI 检查的基础上具有可评估性。基于 3D 解剖图像,使用体素形态计量学来估计基线和随访时的区域脑体积。绘制了组内的纵向体积变化及其与一般认知状态和特定认知领域变化的关系。
作为一个整体,在基底前脑的无名质区域、海马体、外侧颞叶皮质和左侧弓状束中发现了明显的体积减少。在随访期间,临床状态从认知稳定变为轻度认知障碍或痴呆的个体中,无名质和海马体的体积减少更为明显。重要的是,纵向记忆评分变化与海马体的体积变化特异性相关,前瞻性记忆与前额叶相关,言语理解与语言相关脑区相关。
尽管唐氏综合征在发育过程中积累了密集的基线病理学,但结果与阿尔茨海默病进展为痴呆的既定解剖学变化明显一致。这种共性支持唐氏综合征作为阿尔茨海默氏神经退行性变的遗传模型的潜在价值,并可能进一步支持唐氏综合征患者是从阿尔茨海默病治疗研究中获益的最佳候选者的观点。