Department of Psychology, University of Edinburgh, 7 George Square, Edinburgh EH8 9JZ, UK.
Nature. 2012 Jan 18;482(7384):212-5. doi: 10.1038/nature10781.
Understanding the determinants of healthy mental ageing is a priority for society today. So far, we know that intelligence differences show high stability from childhood to old age and there are estimates of the genetic contribution to intelligence at different ages. However, attempts to discover whether genetic causes contribute to differences in cognitive ageing have been relatively uninformative. Here we provide an estimate of the genetic and environmental contributions to stability and change in intelligence across most of the human lifetime. We used genome-wide single nucleotide polymorphism (SNP) data from 1,940 unrelated individuals whose intelligence was measured in childhood (age 11 years) and again in old age (age 65, 70 or 79 years). We use a statistical method that allows genetic (co)variance to be estimated from SNP data on unrelated individuals. We estimate that causal genetic variants in linkage disequilibrium with common SNPs account for 0.24 of the variation in cognitive ability change from childhood to old age. Using bivariate analysis, we estimate a genetic correlation between intelligence at age 11 years and in old age of 0.62. These estimates, derived from rarely available data on lifetime cognitive measures, warrant the search for genetic causes of cognitive stability and change.
理解健康心理衰老的决定因素是当今社会的当务之急。到目前为止,我们知道智力差异在儿童期到老年期表现出高度的稳定性,并且可以估计不同年龄的智力遗传贡献。然而,试图发现遗传原因是否会导致认知衰老的差异的尝试相对来说并没有提供太多信息。在这里,我们提供了一个横跨人类大部分生命周期的智力稳定性和变化的遗传和环境贡献的估计。我们使用了来自 1940 名无血缘关系个体的全基因组单核苷酸多态性 (SNP) 数据,这些个体的智力在儿童期(11 岁)和老年期(65、70 或 79 岁)进行了测量。我们使用了一种统计方法,可以从无血缘关系个体的 SNP 数据中估计遗传(共)方差。我们估计与常见 SNP 处于连锁不平衡状态的因果遗传变异解释了从儿童期到老年期认知能力变化的 0.24。使用双变量分析,我们估计 11 岁时智力与老年时智力的遗传相关性为 0.62。这些估计值来自于对终生认知测量数据的难得获取,这值得我们去寻找认知稳定性和变化的遗传原因。