Department of Psychology, The University of Edinburgh, Edinburgh, UK; Centre for Cognitive Ageing and Cognitive Epidemiology, The University of Edinburgh, Edinburgh, UK.
Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK; Brain Research Imaging Centre, the University of Edinburgh, Edinburgh, UK; Scottish Imaging Network, A Platform for Scientific Excellence (SINAPSE) Collaboration; Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK.
Neurobiol Aging. 2018 Feb;62:146-158. doi: 10.1016/j.neurobiolaging.2017.10.005. Epub 2017 Oct 16.
Fully characterizing age differences in the brain is a key task for combating aging-related cognitive decline. Using propensity score matching on 2 independent, narrow-age cohorts, we used data on childhood cognitive ability, socioeconomic background, and intracranial volume to match participants at mean age of 92 years (n = 42) to very similar participants at mean age of 73 years (n = 126). Examining a variety of global and regional structural neuroimaging variables, there were large differences in gray and white matter volumes, cortical surface area, cortical thickness, and white matter hyperintensity volume and spatial extent. In a mediation analysis, the total volume of white matter hyperintensities and total cortical surface area jointly mediated 24.9% of the relation between age and general cognitive ability (tissue volumes and cortical thickness were not significant mediators in this analysis). These findings provide an unusual and valuable perspective on neurostructural aging, in which brains from the 8th and 10th decades of life differ widely despite the same cognitive, socioeconomic, and brain-volumetric starting points.
充分描述大脑在年龄上的差异是对抗与衰老相关的认知能力下降的关键任务。我们使用了两个独立的、年龄相近的队列的倾向评分匹配,使用了儿童认知能力、社会经济背景和颅内体积的数据来匹配平均年龄为 92 岁的参与者(n=42)和平均年龄为 73 岁的非常相似的参与者(n=126)。研究了多种全局和区域结构神经影像学变量,发现灰质和白质体积、皮质表面积、皮质厚度以及白质高信号体积和空间范围存在很大差异。在中介分析中,白质高信号总体积和总皮质表面积共同介导了年龄与一般认知能力之间 24.9%的关系(在该分析中,组织体积和皮质厚度不是显著的中介因素)。这些发现为神经结构衰老提供了一个不同寻常且有价值的视角,尽管认知、社会经济和脑容量起点相同,但 80 岁和 100 岁的大脑之间存在广泛差异。