The genetic relationships between brain structure and schizophrenia
Eva-Maria Stauffer (),
Richard A. I. Bethlehem,
Lena Dorfschmidt,
Hyejung Won,
Varun Warrier and
Edward T. Bullmore
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Eva-Maria Stauffer: University of Cambridge
Richard A. I. Bethlehem: University of Cambridge
Lena Dorfschmidt: University of Cambridge
Hyejung Won: University of North Carolina at Chapel Hill
Varun Warrier: University of Cambridge
Edward T. Bullmore: University of Cambridge
Nature Communications, 2023, vol. 14, issue 1, 1-15
Abstract:
Abstract Genetic risks for schizophrenia are theoretically mediated by genetic effects on brain structure but it has been unclear which genes are associated with both schizophrenia and cortical phenotypes. We accessed genome-wide association studies (GWAS) of schizophrenia (N = 69,369 cases; 236,642 controls), and of three magnetic resonance imaging (MRI) metrics (surface area, cortical thickness, neurite density index) measured at 180 cortical areas (N = 36,843, UK Biobank). Using Hi-C-coupled MAGMA, 61 genes were significantly associated with both schizophrenia and one or more MRI metrics. Whole genome analysis with partial least squares demonstrated significant genetic covariation between schizophrenia and area or thickness of most cortical regions. Genetic similarity between cortical areas was strongly coupled to their phenotypic covariance, and genetic covariation between schizophrenia and brain phenotypes was strongest in the hubs of structural covariance networks. Pleiotropically associated genes were enriched for neurodevelopmental processes and positionally concentrated in chromosomes 3p21, 17q21 and 11p11. Mendelian randomization analysis indicated that genetically determined variation in a posterior cingulate cortical area could be causal for schizophrenia. Parallel analyses of GWAS on bipolar disorder, Alzheimer’s disease and height showed that pleiotropic association with MRI metrics was stronger for schizophrenia compared to other disorders.
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43567-7
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DOI: 10.1038/s41467-023-43567-7
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