Lövdén Martin, Li Shu-Chen, Shing Yee Lee, Lindenberger Ulman
Center for Lifespan Psychology, Max Planck Institute for Human Development, Lentzeallée 94, D-14195 Berlin, Germany.
Neuropsychologia. 2007 Sep 20;45(12):2827-38. doi: 10.1016/j.neuropsychologia.2007.05.005. Epub 2007 May 17.
Neurocomputational modeling and empirical evidence suggest that losses in neuronal signaling fidelity cause senescent changes in behavior. We applied structural equation modeling to five-occasion 13-year longitudinal data from the Berlin Aging Study (n=447; age range at t1=70-102 years) to test whether trial-to-trial reaction time variability in perceptual speed (identical pictures) antecedes and signals longitudinal decline in levels of performance on perceptual speed (digit letter and identical pictures) and ideational fluency (category fluency). Higher trial-to-trial variability preceded and predicted greater cognitive decline in perceptual speed and ideational fluency. We conclude that trial-to-trial variability signals impending decline in cognitive performance, and that theories of neurocognitive aging need to postulate developmental cascades between senescent changes in variability and central tendency.
神经计算模型和实证证据表明,神经元信号保真度的丧失会导致行为的衰老变化。我们将结构方程模型应用于来自柏林衰老研究的五次测量、为期13年的纵向数据(n = 447;t1时年龄范围为70 - 102岁),以检验在感知速度(相同图片)方面逐次试验的反应时间变异性是否先于并预示着感知速度(数字字母和相同图片)和观念流畅性(类别流畅性)表现水平的纵向下降。更高的逐次试验变异性先于并预测了感知速度和观念流畅性方面更大的认知衰退。我们得出结论,逐次试验变异性预示着认知表现即将下降,并且神经认知衰老理论需要假定变异性和集中趋势的衰老变化之间存在发展级联。