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Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

  • the ENIGMA-CNV working group
  • Maastricht University
  • Cardiff University
  • University of Minnesota Twin Cities
  • University of Oslo
  • University of Amsterdam
  • Karolinska Institutet
  • Diakonhjemmet Hospital
  • University of Melbourne
  • Curtin University
  • Centre Borelli
  • Établissement Public de Santé Barthélémy Durand
  • Heidelberg University 
  • University of Toronto
  • Toronto General Hospital
  • University of California at Los Angeles
  • University of Texas Rio Grande Valley
  • Vrije Universiteit Amsterdam
  • Amsterdam UMC
  • University of Greifswald
  • Emory University
  • University of Newcastle
  • King's College London
  • National Female Hormone Clinic
  • San Juan de Dios Sanitary Park
  • Hospital Universitario Virgen del Rocio
  • South African Medical Research Council
  • University of Cape Town
  • Queensland University of Technology
  • University of Galway
  • Public Health Wales
  • Oslo New University College
  • Université Paris-Saclay
  • University of Vermont
  • Boston Children's Hospital
  • Harvard University
  • University of Utah
  • University of Nottingham
  • Roehampton University
  • Illinois Institute of Technology
  • University of Bergen
  • Norwegian University of Science and Technology
  • Charité – Universitätsmedizin Berlin
  • Partner Site Berlin
  • University of Hamburg
  • University of Montreal
  • University of Southern California
  • University of Groningen
  • Université de Bordeaux
  • Georgia State University
  • University of New South Wales
  • Neuroscience Research Australia
  • University of Pennsylvania
  • Children's Hospital of Philadelphia
  • University of Rome La Sapienza
  • University of Queensland
  • Queensland Institute of Medical Research
  • Royal College of Surgeons in Ireland
  • University Hospital of Schleswig-Holstein
  • Sorbonne Université
  • McGill University
  • University of Göttingen
  • Hammersmith Hospital
  • Prince of Wales Hospital
  • Fudan University
  • German Centre for Cardiovascular Research
  • Instituto de Física de Cantabria
  • Hospital Universitario Marques de Valdecilla
  • Technische Universität Dresden
  • Charles R. Drew University of Medicine and Science
  • Universidad de Cantabria

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Copy number variants (CNVs) may increase the risk for neurodevelopmental conditions. The neurobiological mechanisms that link these high-risk genetic variants to clinical phenotypes are largely unknown. An important question is whether brain abnormalities in individuals who carry CNVs are associated with their degree of penetrance. Methods: We investigated whether increased CNV penetrance for schizophrenia and other developmental disorders was associated with variations in cortical and subcortical morphology. We pooled T1-weighted brain magnetic resonance imaging and genetic data from 22 cohorts from the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis)-CNV consortium. In the main analyses, we included 9268 individuals (aged 7–90 years, 54% female), from which we identified 398 carriers of 36 neurodevelopmental CNVs at 20 distinct loci. A secondary analysis was performed including additional neuroimaging data from the ENIGMA-22q consortium, including 274 carriers of the 22q11.2 deletion and 291 noncarriers. CNV penetrance was estimated through penetrance scores that were previously generated from large cohorts of patients and controls. These scores represent the probability risk of developing either schizophrenia or other developmental disorders (including developmental delay, autism spectrum disorder, and congenital malformations). Results: For both schizophrenia and developmental disorders, increased penetrance scores were associated with lower surface area in the cerebral cortex and lower intracranial volume. For both conditions, associations between CNV-penetrance scores and cortical surface area were strongest in regions of the occipital lobes, specifically in the cuneus and lingual gyrus. Conclusions: Our findings link global and regional cortical morphometric features with CNV penetrance, providing new insights into neurobiological mechanisms of genetic risk for schizophrenia and other developmental disorders.

Original languageEnglish
Pages (from-to)1093-1106
Number of pages14
JournalBiological Psychiatry: Cognitive Neuroscience and Neuroimaging
Volume10
Issue number10
DOIs
Publication statusPublished - Oct 2025

Keywords

  • Autism
  • Neuroimaging
  • Psychiatric disorders
  • Schizophrenia
  • Structural imaging

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