Associated Genetics and Connectomic Circuitry in Schizophrenia and Bipolar Disorder.

Biol Psychiatry

Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands; Department of Child and Adolescent Psychiatry and Psychology, Section Complex Trait Genetics, Amsterdam Neuroscience, Vrije Universiteit Medical Center, Amsterdam UMC, Amsterdam, the Netherlands. Electronic address:

Published: July 2023

AI Article Synopsis

  • Schizophrenia (SCZ) and bipolar disorder (BD) are severe mental health disorders that share similar symptoms and genetic backgrounds, and may have overlapping effects on brain connectivity.
  • The study analyzed data from nearly 20,000 healthy individuals to examine how genetic risks for SCZ and BD affect brain connectivity using advanced imaging techniques and genome-wide association studies.
  • Results indicated significant links between specific brain regions and genetic risks for both disorders, identifying multiple genomic loci associated with brain circuits relevant to SCZ and BD, supporting the idea that these genetic factors influence brain structure even in healthy individuals.

Article Abstract

Background: Schizophrenia (SCZ) and bipolar disorder (BD) are severe psychiatric conditions that can involve symptoms of psychosis and cognitive dysfunction. The 2 conditions share symptomatology and genetic etiology and are regularly hypothesized to share underlying neuropathology. Here, we examined how genetic liability to SCZ and BD shapes normative variations in brain connectivity.

Methods: We examined the effect of the combined genetic liability for SCZ and BD on brain connectivity from two perspectives. First, we examined the association between polygenic scores for SCZ and BD for 19,778 healthy subjects from the UK Biobank and individual variation in brain structural connectivity reconstructed by means of diffusion weighted imaging data. Second, we conducted genome-wide association studies using genotypic and imaging data from the UK Biobank, taking SCZ-/BD-involved brain circuits as phenotypes of interest.

Results: Our findings showed brain circuits of superior parietal and posterior cingulate regions to be associated with polygenic liability for SCZ and BD, circuitry that overlaps with brain networks involved in disease conditions (r = 0.239, p < .001). Genome-wide association study analysis showed 9 significant genomic loci associated with SCZ-involved circuits and 14 loci associated with BD-involved circuits. Genes related to SCZ-/BD-involved circuits were significantly enriched in gene sets previously reported in genome-wide association studies for SCZ and BD.

Conclusions: Our findings suggest that polygenic liability of SCZ and BD is associated with normative individual variation in brain circuitry.

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Source
http://dx.doi.org/10.1016/j.biopsych.2022.11.006DOI Listing

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