Genetic influence on cognitive development between childhood and adulthood

被引:0
作者
Josephine Mollon
Emma E. M. Knowles
Samuel R. Mathias
Ruben Gur
Juan Manuel Peralta
Daniel J. Weiner
Elise B. Robinson
Raquel E. Gur
John Blangero
Laura Almasy
David C. Glahn
机构
[1] Yale University School of Medicine,Department of Psychiatry
[2] University of Pennsylvania,Department of Psychiatry, Perelman School of Medicine, and the Penn
[3] University of Texas of the Rio Grande Valley,CHOP Lifespan Brain Institute
[4] Massachusetts General Hospital and Harvard Medical School,South Texas Diabetes and Obesity Institute, School of Medicine
[5] Broad Institute of MIT and Harvard,Analytic and Translational Genetics Unit, Department of Medicine
[6] Broad Institute of MIT and Harvard,Stanley Center for Psychiatric Research
[7] University of Pennsylvania,Program in Medical and Population Genetics
[8] Institute of Living,Department of Genetics, Perelman School of Medicine, and the Penn
来源
Molecular Psychiatry | 2021年 / 26卷
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摘要
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.
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页码:656 / 665
页数:9
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共 259 条
[31]  
Lowe JK(2004)Genetic and environmental contributions to general cognitive ability through the first 16 years of life Dev Psychol 40 581-99
[32]  
Tian Y(1993)Statistical genetic approaches to human adaptability Hum Biol 65 1356-89
[33]  
Horvath S(2012)Genotypexage interaction in human transcriptional ageing Mech Ageing Dev 133 1181-11
[34]  
Johnson MB(2015)The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative J Child Psychol Psychiatry 56 251-59
[35]  
Kawasawa YI(2007)The NCBI dbGaP database of genotypes and phenotypes Nat Genet 39 254-21
[36]  
Mason CE(2012)Age group and sex differences in performance on a computerized neurocognitive battery in children age 8–21 Neuropsychology 26 377-9
[37]  
Krsnik Ž(2010)A cognitive neuroscience-based computerized battery for efficient measurement of individual differences: standardization and initial construct validation J Neurosci Methods 187 473-201
[38]  
Coppola G(2011)Multiple imputation using chained equations: issues and guidance for practice Stat Med 30 b2393-75
[39]  
Bogdanović D(1996)Multiple imputation after 18+years J Am Stat Assoc 91 205-800
[40]  
Haworth CM(2009)Multiple imputation for missing data in epidemiological and clinical research: potential and pitfalls BMJ 338 541-7