Department of Psychology, University of Oslo Oslo, Norway.
Front Aging Neurosci. 2010 Nov 2;2:143. doi: 10.3389/fnagi.2010.00143. eCollection 2010.
Knowledge of genetic influences on cognitive aging can constrain and guide interventions aimed at limiting age-related cognitive decline in older adults. Progress in understanding the neural basis of cognitive aging also requires a better understanding of the neurogenetics of cognition. This selective review article describes studies aimed at deriving specific neurogenetic information from three parallel and interrelated phenotype-based approaches: psychometric constructs, cognitive neuroscience-based processing measures, and brain imaging morphometric data. Developments in newer genetic analysis tools, including genome wide association, are also described. In particular, we focus on models for establishing genotype-phenotype associations within an explanatory framework linking molecular, brain, and cognitive levels of analysis. Such multiple-phenotype approaches indicate that individual variation in genes central to maintaining synaptic integrity, neurotransmitter function, and synaptic plasticity are important in affecting age-related changes in brain structure and cognition. Investigating phenotypes at multiple levels is recommended as a means to advance understanding of the neural impact of genetic variants relevant to cognitive aging. Further knowledge regarding the mechanisms of interaction between genetic and preventative procedures will in turn help in understanding the ameliorative effect of various experiential and lifestyle factors on age-related cognitive decline.
对认知老化的遗传影响的了解可以限制和指导旨在限制老年人认知能力下降的干预措施。理解认知老化的神经基础也需要更好地了解认知的神经遗传学。本文综述了旨在从三种平行且相互关联的基于表型的方法中得出特定神经遗传学信息的研究:心理测量结构、基于认知神经科学的处理测量和脑成像形态计量数据。还描述了包括全基因组关联在内的更新遗传分析工具的发展。特别是,我们专注于在将分子、大脑和认知分析水平联系起来的解释框架内建立基因型-表型关联的模型。这些多表型方法表明,维持突触完整性、神经递质功能和突触可塑性的基因的个体变异在影响与认知老化相关的大脑结构和认知的年龄相关变化方面很重要。建议采用多种表型方法来深入了解与认知老化相关的遗传变异对神经的影响。进一步了解遗传和预防措施之间相互作用的机制反过来将有助于理解各种经验和生活方式因素对与年龄相关的认知能力下降的改善作用。