Cambridge Intellectual and Developmental Disabilities Research Group, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Institute of Science and Technology for Brain-inspired Intelligence, Fudan University, Shanghai, China.
Hum Brain Mapp. 2019 Oct 15;40(15):4551-4563. doi: 10.1002/hbm.24720. Epub 2019 Jul 26.
Down's syndrome is a chromosomal disorder that invariably results in both intellectual disability and Alzheimer's disease neuropathology. However, only a limited number of studies to date have investigated intrinsic brain network organisation in people with Down's syndrome, none of which addressed the links between functional connectivity and Alzheimer's disease. In this cross-sectional study, we employed C-Pittsburgh Compound-B (PiB) positron emission tomography in order to group participants with Down's syndrome based on the presence of fibrillar beta-amyloid neuropathology. We also acquired resting state functional magnetic resonance imaging data to interrogate the connectivity of the default mode network; a large-scale system with demonstrated links to Alzheimer's disease. The results revealed widespread positive connectivity of the default mode network in people with Down's syndrome (n = 34, ages 30-55, median age = 43.5) and a stark lack of anti-correlation. However, in contrast to typically developing controls (n = 20, ages 30-55, median age = 43.5), the Down's syndrome group also showed significantly weaker connections in localised frontal and posterior brain regions. Notably, while a comparison of the PiB-negative Down's syndrome group (n = 19, ages 30-48, median age = 41.0) to controls suggested that alterations in default mode connectivity to frontal brain regions are related to atypical development, a comparison of the PiB-positive (n = 15, ages 39-55, median age = 48.0) and PiB-negative Down's syndrome groups indicated that aberrant connectivity in posterior cortices is associated with the presence of Alzheimer's disease neuropathology. Such distinct profiles of altered connectivity not only further our understanding of the brain physiology that underlies these two inherently linked conditions but may also potentially provide a biomarker for future studies of neurodegeneration in people with Down's syndrome.
唐氏综合征是一种染色体疾病,它总是导致智力残疾和阿尔茨海默病神经病理学。然而,迄今为止,只有少数研究调查了唐氏综合征患者的内在大脑网络组织,没有一项研究涉及功能连接与阿尔茨海默病之间的联系。在这项横断面研究中,我们使用 C-Pittsburgh 化合物-B(PiB)正电子发射断层扫描,根据纤维状β-淀粉样蛋白神经病理学将唐氏综合征患者分组。我们还获得了静息状态功能磁共振成像数据,以探讨默认模式网络的连接;这是一个具有与阿尔茨海默病相关的大型系统。结果表明,唐氏综合征患者的默认模式网络存在广泛的正连接(n = 34,年龄 30-55 岁,中位数年龄 = 43.5),并且缺乏明显的反相关。然而,与正常发育的对照组(n = 20,年龄 30-55 岁,中位数年龄 = 43.5)相比,唐氏综合征组的局部额和后脑区域的连接也明显较弱。值得注意的是,虽然将 PiB 阴性唐氏综合征组(n = 19,年龄 30-48 岁,中位数年龄 = 41.0)与对照组进行比较表明,默认模式连接到额叶大脑区域的改变与非典型发育有关,但将 PiB 阳性(n = 15,年龄 39-55 岁,中位数年龄 = 48.0)和 PiB 阴性唐氏综合征组进行比较表明,后皮质的异常连接与阿尔茨海默病神经病理学的存在有关。这种改变的连接的独特模式不仅进一步了解了这两种内在相关疾病的大脑生理学,而且可能为唐氏综合征患者的神经退行性变的未来研究提供生物标志物。