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Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

  • Else Eising
  • , Nazanin Mirza-Schreiber
  • , Eveline L. de Zeeuw
  • , Carol A. Wang
  • , Dongnhu T. Truong
  • , Andrea G. Allegrini
  • , Chin Yang Shapland
  • , Gu Zhu
  • , Karen G. Wigg
  • , Margot L. Gerritse
  • , Barbara Molz
  • , Gökberk Alagöz
  • , Alessandro Gialluisi
  • , Filippo Abbondanza
  • , Kaili Rimfeld
  • , Marjolein van Donkelaar
  • , Zhijie Liao
  • , Philip R. Jansen
  • , Till F.M. Andlauer
  • , Timothy C. Bates
  • Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D. Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S. Dale, Peter F. de Jong, John C. DeFries, Jean François Démonet, Ditte Demontis, Yu Feng, Scott D. Gordon, Sharon L. Guger, Marianna E. Hayiou-Thomas, Juan A. Hernández-Cabrera, Jouke Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N. Kerr, Tanner Koomar, Karin Landerl, Gabriel T. Leonard, Maureen W. Lovett, Heikki Lyytinen, Nicholas G. Martin, Angela Martinelli, Urs Maurer, Jacob J. Michaelson, Kristina Moll, Anthony P. Monaco, Angela T. Morgan, Markus M. Nöthen, Zdenka Pausova, Craig E. Pennell, Bruce F. Pennington, Kaitlyn M. Price, Veera M. Rajagopal, Franck Ramus, Louis Richer, Nuala H. Simpson, Shelley D. Smith, Margaret J. Snowling, John Stein, Lisa J. Strug, Joel B. Talcott, Henning Tiemeier, Marc P. van der Schroeff, Ellen Verhoef, Kate E. Watkins, Margaret Wilkinson, Margaret J. Wright, Cathy L. Barr, Dorret I. Boomsma, Manuel Carreiras, Marie Christine J. Franken, Jeffrey R. Gruen, Michelle Luciano, Bertram Müller-Myhsok, Dianne F. Newbury, Richard K. Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte-Körne, J. Bruce Tomblin, Elsje van Bergen, Andrew J.O. Whitehouse, Erik G. Willcutt, Beate St Pourcain, Clyde Francks, Simon E. Fisher
  • Max Planck Institute for Psycholinguistics
  • Helmholtz Zentrum München/Institute of Epidemiology I
  • Vrije Universiteit Amsterdam
  • School of Medicine and Public Health
  • Hunter Medical Research Institute, Australia
  • Yale University
  • King's College London
  • University of Bristol
  • Bristol Medical School
  • QIMR Berghofer Medical Research Institute
  • University Health Network University of Toronto
  • Max Planck Institute of Psychiatry
  • Latina and IRCCS Neuromed
  • Universita degli Studi dell'Insubria
  • School of Medicine
  • Cass Business School
  • University of Toronto
  • Erasmus University Medical Center
  • VU University Medical Centre
  • Klinikum rechts der Isar der Technischen Universität München
  • Edinburgh Napier University
  • Hospital for Sick Children Research Institute
  • Universiteit Maastricht
  • Aarhus University
  • Lundbeck Foundation Initiative for Integrative Psychiatric Research
  • Center for Genomics and Personalized Medicine (CGPM)
  • CNRS Centre National de la Recherche Scientifique
  • Universität Zürich
  • Heidelberg University
  • Università degli Studi di Bologna
  • Oxford Brookes University
  • Research Centre of Natural Sciences of the Hungarian Academy of Sciences
  • Pannon Egyetem
  • University of New Mexico
  • Universiteit van Amsterdam
  • University of Colorado Boulder
  • Department of Clinical Neurosciences Lausanne University Hospital (CHUV)
  • University of York
  • Departamento de Psicología Clínica Psicobiología y Metodología
  • University of Oxford
  • Karolinska Institutet
  • Helsingin yliopisto
  • Iowa State University
  • University of Graz and BioTechMed
  • BioTechMed-Graz
  • McGill University
  • University of Jyväskylä
  • Chinese University of Hong Kong
  • Ludwig Maximilian University
  • Tufts University
  • Royal Children's Hospital, Melbourne
  • University of Bonn
  • John Hunter Hospital
  • University of Denver
  • University of Toronto Faculty of Medicine
  • Ecole Normale Supérieure
  • Université du Québec à Chicoutimi
  • Oxford University
  • University of Nebraska Medical Center
  • St. John's College, Oxford
  • Hospital for Sick Children
  • Harvard University
  • University of Queensland
  • Netherlands Twin Register
  • Amsterdam Reproduction and Development
  • Brain and Language
  • Ikerbasque, Basque Foundation for Science
  • Universidad del País Vasco
  • Royal Liverpool University Hospital
  • University of Montreal
  • Murdoch Children's Research Institute
  • Menzies Health Institute Queensland
  • Telethon Kids Institute
  • Donders Institute for Brain, Cognition and Behaviour
  • Radboud University Medical Center

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Abstract

The use of spoken and written language is a fundamental human capacity. Individual differences in reading- and language-related skills are influenced by genetic variation, with twin-based heritability estimates of 30 to 80% depending on the trait. The genetic architecture is complex, heterogeneous, and multifactorial, but investigations of contributions of single-nucleotide polymorphisms (SNPs) were thus far underpowered. We present a multicohort genome-wide association study (GWAS) of five traits assessed individually using psychometric measures (word reading, nonword reading, spelling, phoneme awareness, and nonword repetition) in samples of 13,633 to 33,959 participants aged 5 to 26 y. We identified genome-wide significant association with word reading (rs11208009, P = 1.098 × 10-8) at a locus that has not been associated with intelligence or educational attainment. All five reading-/language-related traits showed robust SNP heritability, accounting for 13 to 26% of trait variability. Genomic structural equation modeling revealed a shared genetic factor explaining most of the variation in word/nonword reading, spelling, and phoneme awareness, which only partially overlapped with genetic variation contributing to nonword repetition, intelligence, and educational attainment. A multivariate GWAS of word/nonword reading, spelling, and phoneme awareness maximized power for follow-up investigation. Genetic correlation analysis with neuroimaging traits identified an association with the surface area of the banks of the left superior temporal sulcus, a brain region linked to the processing of spoken and written language. Heritability was enriched for genomic elements regulating gene expression in the fetal brain and in chromosomal regions that are depleted of Neanderthal variants. Together, these results provide avenues for deciphering the biological underpinnings of uniquely human traits.

Original languageEnglish
Article numbere2202764119
Number of pages12
JournalProceedings of the National Academy of Sciences of the United States of America
Volume119
Issue number35
DOIs
Publication statusPublished - 23 Aug 2022

Bibliographical note

Copyright © 2022 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).

Keywords

  • genome-wide association study
  • language
  • meta-analysis
  • reading

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