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ABSTRACT: Objective
To investigate the genetic architecture of internalizing symptoms in childhood and adolescence.Method
In 22 cohorts, multiple univariate genome-wide association studies (GWASs) were performed using repeated assessments of internalizing symptoms, in a total of 64,561 children and adolescents between 3 and 18 years of age. Results were aggregated in meta-analyses that accounted for sample overlap, first using all available data, and then using subsets of measurements grouped by rater, age, and instrument.Results
The meta-analysis of overall internalizing symptoms (INToverall) detected no genome-wide significant hits and showed low single nucleotide polymorphism (SNP) heritability (1.66%, 95% CI = 0.84-2.48%, neffective = 132,260). Stratified analyses indicated rater-based heterogeneity in genetic effects, with self-reported internalizing symptoms showing the highest heritability (5.63%, 95% CI = 3.08%-8.18%). The contribution of additive genetic effects on internalizing symptoms appeared to be stable over age, with overlapping estimates of SNP heritability from early childhood to adolescence. Genetic correlations were observed with adult anxiety, depression, and the well-being spectrum (|rg| > 0.70), as well as with insomnia, loneliness, attention-deficit/hyperactivity disorder, autism, and childhood aggression (range |rg| = 0.42-0.60), whereas there were no robust associations with schizophrenia, bipolar disorder, obsessive-compulsive disorder, or anorexia nervosa.Conclusion
Genetic correlations indicate that childhood and adolescent internalizing symptoms share substantial genetic vulnerabilities with adult internalizing disorders and other childhood psychiatric traits, which could partially explain both the persistence of internalizing symptoms over time and the high comorbidity among childhood psychiatric traits. Reducing phenotypic heterogeneity in childhood samples will be key in paving the way to future GWAS success.
SUBMITTER: Jami ES
PROVIDER: S-EPMC10859168 | biostudies-literature | 2022 Jul
REPOSITORIES: biostudies-literature
Jami Eshim S ES Hammerschlag Anke R AR Ip Hill F HF Allegrini Andrea G AG Benyamin Beben B Border Richard R Diemer Elizabeth W EW Jiang Chang C Karhunen Ville V Lu Yi Y Lu Qing Q Mallard Travis T TT Mishra Pashupati P PP Nolte Ilja M IM Palviainen Teemu T Peterson Roseann E RE Sallis Hannah M HM Shabalin Andrey A AA Tate Ashley E AE Thiering Elisabeth E Vilor-Tejedor Natàlia N Wang Carol C Zhou Ang A Adkins Daniel E DE Alemany Silvia S Ask Helga H Chen Qi Q Corley Robin P RP Ehli Erik A EA Evans Luke M LM Havdahl Alexandra A Hagenbeek Fiona A FA Hakulinen Christian C Henders Anjali K AK Hottenga Jouke Jan JJ Korhonen Tellervo T Mamun Abdullah A Marrington Shelby S Neumann Alexander A Rimfeld Kaili K Rivadeneira Fernando F Silberg Judy L JL van Beijsterveldt Catharina E CE Vuoksimaa Eero E Whipp Alyce M AM Tong Xiaoran X Andreassen Ole A OA Boomsma Dorret I DI Brown Sandra A SA Burt S Alexandra SA Copeland William W Dick Danielle M DM Harden K Paige KP Harris Kathleen Mullan KM Hartman Catharina A CA Heinrich Joachim J Hewitt John K JK Hopfer Christian C Hypponen Elina E Jarvelin Marjo-Riitta MR Kaprio Jaakko J Keltikangas-Järvinen Liisa L Klump Kelly L KL Krauter Kenneth K Kuja-Halkola Ralf R Larsson Henrik H Lehtimäki Terho T Lichtenstein Paul P Lundström Sebastian S Maes Hermine H HH Magnus Per P Munafò Marcus R MR Najman Jake M JM Njølstad Pål R PR Oldehinkel Albertine J AJ Pennell Craig E CE Plomin Robert R Reichborn-Kjennerud Ted T Reynolds Chandra C Rose Richard J RJ Smolen Andrew A Snieder Harold H Stallings Michael M Standl Marie M Sunyer Jordi J Tiemeier Henning H Wadsworth Sally J SJ Wall Tamara L TL Whitehouse Andrew J O AJO Williams Gail M GM Ystrøm Eivind E Nivard Michel G MG Bartels Meike M Middeldorp Christel M CM
Journal of the American Academy of Child and Adolescent Psychiatry 20220401 7
<h4>Objective</h4>To investigate the genetic architecture of internalizing symptoms in childhood and adolescence.<h4>Method</h4>In 22 cohorts, multiple univariate genome-wide association studies (GWASs) were performed using repeated assessments of internalizing symptoms, in a total of 64,561 children and adolescents between 3 and 18 years of age. Results were aggregated in meta-analyses that accounted for sample overlap, first using all available data, and then using subsets of measurements grou ...[more]