Genetic Liability for Schizophrenia and Childhood Psychopathology in the General Population

Author:

Hannigan Laurie J12ORCID,Askeland Ragna Bugge3,Ask Helga3,Tesli Martin34,Corfield Elizabeth3,Ayorech Ziada12,Helgeland Øyvind56,Magnus Per78,Njølstad Pål Rasmus59,Øyen Anne-Siri110,Stoltenberg Camilla1011,Andreassen Ole A412,Davey Smith George2,Reichborn-Kjennerud Ted313,Havdahl Alexandra12314

Affiliation:

1. Nic Waals Institute, Lovisenberg Diaconal Hospital, Oslo, Norway

2. MRC Integrative Epidemiology Unit (IEU), Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK

3. Department of Mental Disorders, Norwegian Institute of Public Health, Oslo, Norway

4. NORMENT Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway

5. KG Jebsen Center for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway

6. Department of Genetics and Bioinformatics, Health Data and Digitalisation, Norwegian Institute of Public Health, Oslo, Norway

7. Centre for Fertility and Health, Norwegian Institute of Public Health, Oslo, Norway

8. Institute of Health and Society, University of Oslo, Norway

9. Department of Pediatrics and Adolescents, Haukeland University Hospital, Bergen, Norway

10. Norwegian Institute of Public Health, Oslo, Norway

11. Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway

12. Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway

13. Institute of Clinical Medicine, University of Oslo, Oslo, Norway

14. Promenta Research Center, Department of Psychology, University of Oslo, Oslo, Norway

Abstract

Abstract Genetic liability for schizophrenia is associated with psychopathology in early life. It is not clear if these associations are time dependent during childhood, nor if they are specific across different forms of psychopathology. Using genotype and questionnaire data on children (N = 15 105) from the Norwegian Mother, Father and Child Cohort Study, we used schizophrenia polygenic risk scores to test developmental stability in associations with measures of emotional and behavioral problems between 18 months and 5 years, and domain specificity in associations with symptoms of depression, anxiety, conduct problems, oppositionality, inattention, and hyperactivity at 8 years. We then sought to identify symptom profiles—across development and domains—associated with schizophrenia polygenic liability. We found evidence for developmental stability in associations between schizophrenia polygenic risk scores and emotional and behavioral problems, with the latter being mediated specifically via the rate of change in symptoms (β slope = 0.032; 95% CI: 0.007–0.057). At age 8, associations were better explained by a model of symptom-specific polygenic effects rather than effects mediated via a general psychopathology factor or by domain-specific factors. Overall, individuals with higher schizophrenia polygenic risk scores were more likely (OR = 1.310 [95% CIs: 1.122–1.528]) to have a profile of increasing behavioral and emotional symptoms in early childhood, followed by elevated symptoms of conduct disorder, oppositionality, hyperactivity, and inattention by age 8. Schizophrenia-associated alleles are linked to specific patterns of early-life psychopathology. The associations are small, but findings of this nature can help us better understand the developmental emergence of schizophrenia.

Funder

South-Eastern Norway Regional Health Authority

Norwegian Research Council

Research Council of Norway

European Research Council

Stiftelsen Kristian Gerhard Jebsen

Trond Mohn Foundation

Novo Nordisk Foundation

University of Bergen

Western Norway Health Authorities

Helse Vest

H2020

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

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