Exploring the genetic architecture of brain structure and ADHD using polygenic neuroimaging‐derived scores

Author:

van der Es Tim12ORCID,Soheili‐Nezhad Sourena3,Roth Mota Nina4,Franke Barbara45,Buitelaar Jan5,Sprooten Emma45

Affiliation:

1. Social, Genetic and Developmental Psychiatry Centre Institute of Psychiatry, Psychology and Neuroscience, King's College London London UK

2. Genome Institute of Singapore, A*STAR Singapore Singapore

3. Max Planck Institute for Psycholinguistics Nijmegen The Netherlands

4. Department of Human Genetics Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center Nijmegen The Netherlands

5. Department of Cognitive Neuroscience Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center Nijmegen The Netherlands

Abstract

AbstractGenome‐wide association studies (GWAS) have provided valuable insights into the genetic basis of neuropsychiatric disorders and highlighted their complexity. Careful consideration of the polygenicity and complex genetic architecture could aid in the understanding of the underlying brain mechanisms. We introduce an innovative approach to polygenic scoring, utilizing imaging‐derived phenotypes (IDPs) to predict a clinical phenotype. We leveraged IDP GWAS data from the UK Biobank, to create polygenic imaging‐derived scores (PIDSs). As a proof‐of‐concept, we assessed genetic variations in brain structure between individuals with ADHD and unaffected controls across three NeuroIMAGE waves (n = 954). Out of the 94 PIDS, 72 exhibited significant associations with their corresponding IDPs in an independent sample. Notably, several global measures, including cerebellum white matter, cerebellum cortex, and cerebral white matter, displayed substantial variance explained for their respective IDPs, ranging from 3% to 5.7%. Conversely, the associations between each IDP and the clinical ADHD phenotype were relatively weak. These findings highlight the growing power of GWAS in structural neuroimaging traits, enabling the construction of polygenic scores that accurately reflect the underlying polygenic architecture. However, to establish robust connections between PIDS and behavioral or clinical traits such as ADHD, larger samples are needed. Our novel approach to polygenic risk scoring offers a valuable tool for researchers in the field of psychiatric genetics.

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Radboud Universitair Medisch Centrum

Vrije Universiteit Amsterdam

Publisher

Wiley

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