Rare chromosomal deletions and duplications increase risk of schizophrenia

J.L. Stone, M.C. O'Donovan, H. Gurling, G.K. Kirov, D.H.R. Blackwood, A. Corvin, N.J. Craddock, M. Gill, B.S. Pickard, The International Schizophrenia Consortium

Research output: Contribution to journalArticle

1138 Citations (Scopus)

Abstract

Schizophrenia is a severe mental disorder marked by hallucinations, delusions, cognitive deficits and apathy, with a heritability estimated at 73 - 90% ( ref. 1). Inheritance patterns are complex, and the number and type of genetic variants involved are not understood. Copy number variants ( CNVs) have been identified in individual patients with schizophrenia(2-7) and also in neurodevelopmental disorders(8-11), but large- scale genome- wide surveys have not been performed. Here we report a genome- wide survey of rare CNVs in 3,391 patients with schizophrenia and 3,181 ancestrally matched controls, using high- density microarrays. For CNVs that were observed in less than 1% of the sample and were more than 100 kilobases in length, the total burden is increased 1.15- fold in patients with schizophrenia in comparison with controls. This effect was more pronounced for rarer, single- occurrence CNVs and for those that involved genes as opposed to those that did not. As expected, deletions were found within the region critical for velo- cardio- facial syndrome, which includes psychotic symptoms in 30% of patients(12). Associations with schizophrenia were also found for large deletions on chromosome 15q13.3 and 1q21.1. These associations have not previously been reported, and they remained significant after genome- wide correction. Our results provide strong support for a model of schizophrenia pathogenesis that includes the effects of multiple rare structural variants, both genome- wide and at specific loci.
Original languageEnglish
Pages (from-to)237-241
Number of pages5
JournalNature
Volume455
Issue number7210
DOIs
Publication statusPublished - 11 Sep 2008

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Chromosome Duplication
Schizophrenia
Genome
Genomic Structural Variation
DiGeorge Syndrome
Apathy
Inheritance Patterns
Chromosome Deletion
Delusions
Hallucinations
Mental Disorders
Genes

Keywords

  • comparative genomic hybridization
  • low copy repeats
  • disorders
  • rearrangements
  • association
  • linkage
  • number
  • locus
  • microdeletion
  • architecture

Cite this

Stone, J. L., O'Donovan, M. C., Gurling, H., Kirov, G. K., Blackwood, D. H. R., Corvin, A., ... The International Schizophrenia Consortium (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature, 455(7210), 237-241. https://doi.org/10.1038/nature07239
Stone, J.L. ; O'Donovan, M.C. ; Gurling, H. ; Kirov, G.K. ; Blackwood, D.H.R. ; Corvin, A. ; Craddock, N.J. ; Gill, M. ; Pickard, B.S. ; The International Schizophrenia Consortium. / Rare chromosomal deletions and duplications increase risk of schizophrenia. In: Nature. 2008 ; Vol. 455, No. 7210. pp. 237-241.
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Stone, JL, O'Donovan, MC, Gurling, H, Kirov, GK, Blackwood, DHR, Corvin, A, Craddock, NJ, Gill, M, Pickard, BS & The International Schizophrenia Consortium 2008, 'Rare chromosomal deletions and duplications increase risk of schizophrenia', Nature, vol. 455, no. 7210, pp. 237-241. https://doi.org/10.1038/nature07239

Rare chromosomal deletions and duplications increase risk of schizophrenia. / Stone, J.L.; O'Donovan, M.C.; Gurling, H.; Kirov, G.K.; Blackwood, D.H.R.; Corvin, A.; Craddock, N.J.; Gill, M.; Pickard, B.S.; The International Schizophrenia Consortium.

In: Nature, Vol. 455, No. 7210, 11.09.2008, p. 237-241.

Research output: Contribution to journalArticle

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AB - Schizophrenia is a severe mental disorder marked by hallucinations, delusions, cognitive deficits and apathy, with a heritability estimated at 73 - 90% ( ref. 1). Inheritance patterns are complex, and the number and type of genetic variants involved are not understood. Copy number variants ( CNVs) have been identified in individual patients with schizophrenia(2-7) and also in neurodevelopmental disorders(8-11), but large- scale genome- wide surveys have not been performed. Here we report a genome- wide survey of rare CNVs in 3,391 patients with schizophrenia and 3,181 ancestrally matched controls, using high- density microarrays. For CNVs that were observed in less than 1% of the sample and were more than 100 kilobases in length, the total burden is increased 1.15- fold in patients with schizophrenia in comparison with controls. This effect was more pronounced for rarer, single- occurrence CNVs and for those that involved genes as opposed to those that did not. As expected, deletions were found within the region critical for velo- cardio- facial syndrome, which includes psychotic symptoms in 30% of patients(12). Associations with schizophrenia were also found for large deletions on chromosome 15q13.3 and 1q21.1. These associations have not previously been reported, and they remained significant after genome- wide correction. Our results provide strong support for a model of schizophrenia pathogenesis that includes the effects of multiple rare structural variants, both genome- wide and at specific loci.

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Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A et al. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008 Sep 11;455(7210):237-241. https://doi.org/10.1038/nature07239