Mollon Josephine, Knowles Emma E M, Mathias Samuel R, Gur Ruben, Peralta Juan Manuel, Weiner Daniel J, Robinson Elise B, Gur Raquel E, Blangero John, Almasy Laura, Glahn David C
Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
Department of Psychiatry, Perelman School of Medicine, and the Penn-CHOP Lifespan Brain Institute, University of Pennsylvania, Philadelphia, PA, USA.
Mol Psychiatry. 2021 Feb;26(2):656-665. doi: 10.1038/s41380-018-0277-0. Epub 2018 Oct 19.
Successful cognitive development between childhood and adulthood has important consequences for future mental and physical wellbeing, as well as occupational and financial success. Therefore, delineating the genetic influences underlying changes in cognitive abilities during this developmental period will provide important insights into the biological mechanisms that govern both typical and atypical maturation. Using data from the Philadelphia Neurodevelopmental Cohort (PNC), a large population-based sample of individuals aged 8 to 21 years old (n = 6634), we used an empirical relatedness matrix to establish the heritability of general and specific cognitive functions and determine if genetic factors influence cognitive maturation (i.e., Gene × Age interactions) between childhood and early adulthood. We found that neurocognitive measures across childhood and early adulthood were significantly heritable. Moreover, genetic variance on general cognitive ability, or g, increased significantly between childhood and early adulthood. Finally, we did not find evidence for decay in genetic correlation on neurocognition throughout childhood and adulthood, suggesting that the same genetic factors underlie cognition at different ages throughout this developmental period. Establishing significant Gene × Age interactions in neurocognitive functions across childhood and early adulthood is a necessary first step in identifying genes that influence cognitive development, rather than genes that influence cognition per se. Moreover, since aberrant cognitive development confers risk for several psychiatric disorders, further examination of these Gene × Age interactions may provide important insights into their etiology.
儿童期到成年期的认知发展成功对未来的身心健康以及职业和经济成就具有重要影响。因此,阐明这一发育阶段认知能力变化背后的遗传影响,将为支配典型和非典型成熟的生物学机制提供重要见解。利用来自费城神经发育队列(PNC)的数据,这是一个基于人群的8至21岁个体的大样本(n = 6634),我们使用经验相关性矩阵来确定一般和特定认知功能的遗传力,并确定遗传因素是否影响儿童期到成年早期的认知成熟(即基因×年龄相互作用)。我们发现,儿童期和成年早期的神经认知测量具有显著的遗传性。此外,一般认知能力(g)的遗传方差在儿童期到成年早期显著增加。最后,我们没有发现整个儿童期和成年期神经认知遗传相关性衰减的证据,这表明在这个发育阶段的不同年龄,相同的遗传因素是认知的基础。确定儿童期和成年早期神经认知功能中显著的基因×年龄相互作用,是识别影响认知发展的基因而非影响认知本身的基因的必要第一步。此外,由于异常的认知发展会增加多种精神疾病的风险,对这些基因×年龄相互作用的进一步研究可能会为其病因提供重要见解。