Abstract

The association of copy number variation (CNV) with schizophrenia has been reported with evidence of increased frequency of both rare and large CNVs. Yet, little is known about the impact of CNVs in brain structure. In this pilot study, we explored collective effects of all CNVs in each cytogenetic band on the risk of schizophrenia and gray matter variation measured in structural magnetic resonance imaging. With 324 participants’ CNV profiles (151 schizophrenia patients and 173 healthy controls), we first extracted specific CNV features that differ between patients and controls using a two sample t-test, and then tested their associations with gray matter concentration using a linear regression model in a subset of 301 participants. Our data first provided evidence of population structure in CNV features where elevated rare CNV burden in schizophrenia patients was confounded by the levels associated with African American subjects. We considered this ethnic group difference in the following cytoband analyses. Deletions in one cytoband 22q13.31 were observed significantly (p<0.05) more in patients than controls from all samples after controlling ethnicity, and the deletion load was also significantly (p = 1.44×10−4) associated with reduced gray matter concentration of a brain network mainly comprised of the cingulate gyrus and insula. Since 80% deletion carriers were patients, patients with deletions also showed reduced gray matter concentration compared with patients without deletions (p = 3.36×10−4). Our findings indicate that regional CNVs at 22q13.31, no matter the size, may influence the risk of schizophrenia with a remarkably increased mutation rate and with reduced gray matter concentration in the peri-limbic cortex. This proof-of-concept study suggests that the CNVs occurring at some ‘hotspots’ may in fact cause biological downstream effects and larger studies are important for confirming our initial results.

Highlights

  • Schizophrenia (SZ) is a severe mental disorder marked by hallucinations, delusions and cognitive deficits with a heritability estimated at 73–90% [1]

  • We first presented the copy number variation (CNV) profiles, including large CNVs, CNVs in three hot spots associated with SZ, and total CNV burden

  • More rare CNVs and rare deletions were found in patients than controls with p values less than 0.05, this higher rate was confounded by ethnicity

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Summary

Introduction

Schizophrenia (SZ) is a severe mental disorder marked by hallucinations, delusions and cognitive deficits with a heritability estimated at 73–90% [1]. Large CNVs (.100 k bp) at specific regions involving genes in important neuro-developmental pathways, such as NXRN1, ERBB4 and CNTAP2 [15,17,18,19], have hinted to the involvement of developmental alterations in this illness. In addition to these individual large CNVs, the total CNV burden across the whole genome has been associated to many phenotypic variations [20,21,22,23], including schizophrenia with elevated frequencies of large CNVs, rare CNVs, and rare deletions in patients [19,23]

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