Your browser doesn't support javascript.
loading
Schizophrenia Polygenic Risk During Typical Development Reflects Multiscale Cortical Organization.
Kirschner, Matthias; Paquola, Casey; Khundrakpam, Budhachandra S; Vainik, Uku; Bhutani, Neha; Hodzic-Santor, Benazir; Georgiadis, Foivos; Al-Sharif, Noor B; Misic, Bratislav; Bernhardt, Boris C; Evans, Alan C; Dagher, Alain.
Affiliation
  • Kirschner M; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Paquola C; Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zürich, Zürich, Switzerland.
  • Khundrakpam BS; Division of Adult Psychiatry, Department of Psychiatry, University Hospitals of Geneva, Geneva, Switzerland.
  • Vainik U; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Bhutani N; Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany.
  • Hodzic-Santor B; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Georgiadis F; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Al-Sharif NB; Institute of Psychology, Faculty of Social Sciences, Tartu, Estonia.
  • Misic B; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Bernhardt BC; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Evans AC; Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital, University of Zürich, Zürich, Switzerland.
  • Dagher A; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
Biol Psychiatry Glob Open Sci ; 3(4): 1083-1093, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37881579
ABSTRACT

Background:

Schizophrenia is widely recognized as a neurodevelopmental disorder. Abnormal cortical development in otherwise typically developing children and adolescents may be revealed using polygenic risk scores for schizophrenia (PRS-SCZ).

Methods:

We assessed PRS-SCZ and cortical morphometry in typically developing children and adolescents (3-21 years, 46.8% female) using whole-genome genotyping and T1-weighted magnetic resonance imaging (n = 390) from the PING (Pediatric Imaging, Neurocognition, and Genetics) cohort. We contextualized the findings using 1) age-matched transcriptomics, 2) histologically defined cytoarchitectural types and functionally defined networks, and 3) case-control differences of schizophrenia and other major psychiatric disorders derived from meta-analytic data of 6 ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) working groups, including a total of 12,876 patients and 15,670 control participants.

Results:

Higher PRS-SCZ was associated with greater cortical thickness, which was most prominent in areas with heightened gene expression of dendrites and synapses. PRS-SCZ-related increases in vertexwise cortical thickness were mainly distributed in association cortical areas, particularly the ventral attention network, while relatively sparing koniocortical type cortex (i.e., primary sensory areas). The large-scale pattern of cortical thickness increases related to PRS-SCZ mirrored the pattern of cortical thinning in schizophrenia and mood-related psychiatric disorders derived from the ENIGMA consortium. Age group models illustrate a possible trajectory from PRS-SCZ-associated cortical thickness increases in early childhood toward thinning in late adolescence, with the latter resembling the adult brain phenotype of schizophrenia.

Conclusions:

Collectively, combining imaging genetics with multiscale mapping, our work provides novel insight into how genetic risk for schizophrenia affects the cortex early in life.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biol Psychiatry Glob Open Sci Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biol Psychiatry Glob Open Sci Year: 2023 Document type: Article Affiliation country:
...