Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

Detalhes bibliográficos
Autor(a) principal: Thygesen, J. H.
Data de Publicação: 2021
Outros Autores: Presman, A., Harju-Seppänen, J., Irizar, H., Jones, R., Kuchenbaecker, K., Lin, K., Alizadeh, B. Z., Austin-Zimmerman, I., Bartels-Velthuis, A., Bhat, A., Bruggeman, R., Cahn, W., Calafato, S., Crespo-Facorro, B., De Haan, L., De Zwarte, S. M. C., Di Forti, M., Díez-Revuelta, Á., Hall, J., Hall, M.-H., Iyegbe, C., Jablensky, A., Kahn, R., Kalaydjieva, L., Kravariti, E., Lawrie, S., Luykx, J. J., Mata, I., McDonald, C., McIntosh, A. M., McQuillin, A., Muir, R., Ophoff, R., Picchioni, M., Prata, D. P., Ranlund, S., Rujescu, D., Rutten, B. P. F., Schulze, K., Shaikh, M., Schirmbeck, F., Simons, C. J. P., Toulopoulou, T., Van Amelsvoort, T., Van Haren, N., Van Os, J., Van Winkel, R., Vassos, E., Walshe, M., Weisbrod, M., Zartaloudi, E., Bell, V., Powell, J., Lewis, C. M., Murray, R. M., Bramon, E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10071/21570
Resumo: The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs increase the risk of developing schizophrenia. Several cognitive measures are purported schizophrenia endophenotypes and may represent an intermediate point between genetics and the illness. This paper investigates the influence of CNVs on cognition. We conducted a systematic review and meta-analysis of the literature exploring the effect of CNV burden on general intelligence. We included ten primary studies with a total of 18,847 participants and found no evidence of association. In a new psychosis family study, we investigated the effects of CNVs on specific cognitive abilities. We examined the burden of large and rare CNVs (>200 kb, <1% MAF) as well as known schizophrenia-associated CNVs in patients with psychotic disorders, their unaffected relatives and controls (N = 3428) from the Psychosis Endophenotypes International Consortium (PEIC). The carriers of specific schizophrenia-associated CNVs showed poorer performance than non-carriers in immediate (P = 0.0036) and delayed (P = 0.0115) verbal recall. We found suggestive evidence that carriers of schizophrenia-associated CNVs had poorer block design performance (P = 0.0307). We do not find any association between CNV burden and cognition. Our findings show that the known high-risk CNVs are not only associated with schizophrenia and other neurodevelopmental disorders, but are also a contributing factor to impairment in cognitive domains such as memory and perceptual reasoning, and act as intermediate biomarkers of disease risk.
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spelling Genetic copy number variants, cognition and psychosis: a meta-analysis and a family studyThe burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs increase the risk of developing schizophrenia. Several cognitive measures are purported schizophrenia endophenotypes and may represent an intermediate point between genetics and the illness. This paper investigates the influence of CNVs on cognition. We conducted a systematic review and meta-analysis of the literature exploring the effect of CNV burden on general intelligence. We included ten primary studies with a total of 18,847 participants and found no evidence of association. In a new psychosis family study, we investigated the effects of CNVs on specific cognitive abilities. We examined the burden of large and rare CNVs (>200 kb, <1% MAF) as well as known schizophrenia-associated CNVs in patients with psychotic disorders, their unaffected relatives and controls (N = 3428) from the Psychosis Endophenotypes International Consortium (PEIC). The carriers of specific schizophrenia-associated CNVs showed poorer performance than non-carriers in immediate (P = 0.0036) and delayed (P = 0.0115) verbal recall. We found suggestive evidence that carriers of schizophrenia-associated CNVs had poorer block design performance (P = 0.0307). We do not find any association between CNV burden and cognition. Our findings show that the known high-risk CNVs are not only associated with schizophrenia and other neurodevelopmental disorders, but are also a contributing factor to impairment in cognitive domains such as memory and perceptual reasoning, and act as intermediate biomarkers of disease risk.Springer Nature2021-01-26T17:43:19Z2021-01-01T00:00:00Z20212022-04-07T13:24:28Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10071/21570eng1359-418410.1038/s41380-020-0820-7Thygesen, J. H.Presman, A.Harju-Seppänen, J.Irizar, H.Jones, R.Kuchenbaecker, K.Lin, K.Alizadeh, B. Z.Austin-Zimmerman, I.Bartels-Velthuis, A.Bhat, A.Bruggeman, R.Cahn, W.Calafato, S.Crespo-Facorro, B.De Haan, L.De Zwarte, S. M. C.Di Forti, M.Díez-Revuelta, Á.Hall, J.Hall, M.-H.Iyegbe, C.Jablensky, A.Kahn, R.Kalaydjieva, L.Kravariti, E.Lawrie, S.Luykx, J. J.Mata, I.McDonald, C.McIntosh, A. M.McQuillin, A.Muir, R.Ophoff, R.Picchioni, M.Prata, D. P.Ranlund, S.Rujescu, D.Rutten, B. P. F.Schulze, K.Shaikh, M.Schirmbeck, F.Simons, C. J. P.Toulopoulou, T.Van Amelsvoort, T.Van Haren, N.Van Os, J.Van Winkel, R.Vassos, E.Walshe, M.Weisbrod, M.Zartaloudi, E.Bell, V.Powell, J.Lewis, C. M.Murray, R. M.Bramon, E.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-07-07T02:51:51Zoai:repositorio.iscte-iul.pt:10071/21570Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-07-07T02:51:51Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
title Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
spellingShingle Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
Thygesen, J. H.
title_short Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
title_full Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
title_fullStr Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
title_full_unstemmed Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
title_sort Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study
author Thygesen, J. H.
author_facet Thygesen, J. H.
Presman, A.
Harju-Seppänen, J.
Irizar, H.
Jones, R.
Kuchenbaecker, K.
Lin, K.
Alizadeh, B. Z.
Austin-Zimmerman, I.
Bartels-Velthuis, A.
Bhat, A.
Bruggeman, R.
Cahn, W.
Calafato, S.
Crespo-Facorro, B.
De Haan, L.
De Zwarte, S. M. C.
Di Forti, M.
Díez-Revuelta, Á.
Hall, J.
Hall, M.-H.
Iyegbe, C.
Jablensky, A.
Kahn, R.
Kalaydjieva, L.
Kravariti, E.
Lawrie, S.
Luykx, J. J.
Mata, I.
McDonald, C.
McIntosh, A. M.
McQuillin, A.
Muir, R.
Ophoff, R.
Picchioni, M.
Prata, D. P.
Ranlund, S.
Rujescu, D.
Rutten, B. P. F.
Schulze, K.
Shaikh, M.
Schirmbeck, F.
Simons, C. J. P.
Toulopoulou, T.
Van Amelsvoort, T.
Van Haren, N.
Van Os, J.
Van Winkel, R.
Vassos, E.
Walshe, M.
Weisbrod, M.
Zartaloudi, E.
Bell, V.
Powell, J.
Lewis, C. M.
Murray, R. M.
Bramon, E.
author_role author
author2 Presman, A.
Harju-Seppänen, J.
Irizar, H.
Jones, R.
Kuchenbaecker, K.
Lin, K.
Alizadeh, B. Z.
Austin-Zimmerman, I.
Bartels-Velthuis, A.
Bhat, A.
Bruggeman, R.
Cahn, W.
Calafato, S.
Crespo-Facorro, B.
De Haan, L.
De Zwarte, S. M. C.
Di Forti, M.
Díez-Revuelta, Á.
Hall, J.
Hall, M.-H.
Iyegbe, C.
Jablensky, A.
Kahn, R.
Kalaydjieva, L.
Kravariti, E.
Lawrie, S.
Luykx, J. J.
Mata, I.
McDonald, C.
McIntosh, A. M.
McQuillin, A.
Muir, R.
Ophoff, R.
Picchioni, M.
Prata, D. P.
Ranlund, S.
Rujescu, D.
Rutten, B. P. F.
Schulze, K.
Shaikh, M.
Schirmbeck, F.
Simons, C. J. P.
Toulopoulou, T.
Van Amelsvoort, T.
Van Haren, N.
Van Os, J.
Van Winkel, R.
Vassos, E.
Walshe, M.
Weisbrod, M.
Zartaloudi, E.
Bell, V.
Powell, J.
Lewis, C. M.
Murray, R. M.
Bramon, E.
author2_role author
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dc.contributor.author.fl_str_mv Thygesen, J. H.
Presman, A.
Harju-Seppänen, J.
Irizar, H.
Jones, R.
Kuchenbaecker, K.
Lin, K.
Alizadeh, B. Z.
Austin-Zimmerman, I.
Bartels-Velthuis, A.
Bhat, A.
Bruggeman, R.
Cahn, W.
Calafato, S.
Crespo-Facorro, B.
De Haan, L.
De Zwarte, S. M. C.
Di Forti, M.
Díez-Revuelta, Á.
Hall, J.
Hall, M.-H.
Iyegbe, C.
Jablensky, A.
Kahn, R.
Kalaydjieva, L.
Kravariti, E.
Lawrie, S.
Luykx, J. J.
Mata, I.
McDonald, C.
McIntosh, A. M.
McQuillin, A.
Muir, R.
Ophoff, R.
Picchioni, M.
Prata, D. P.
Ranlund, S.
Rujescu, D.
Rutten, B. P. F.
Schulze, K.
Shaikh, M.
Schirmbeck, F.
Simons, C. J. P.
Toulopoulou, T.
Van Amelsvoort, T.
Van Haren, N.
Van Os, J.
Van Winkel, R.
Vassos, E.
Walshe, M.
Weisbrod, M.
Zartaloudi, E.
Bell, V.
Powell, J.
Lewis, C. M.
Murray, R. M.
Bramon, E.
description The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs increase the risk of developing schizophrenia. Several cognitive measures are purported schizophrenia endophenotypes and may represent an intermediate point between genetics and the illness. This paper investigates the influence of CNVs on cognition. We conducted a systematic review and meta-analysis of the literature exploring the effect of CNV burden on general intelligence. We included ten primary studies with a total of 18,847 participants and found no evidence of association. In a new psychosis family study, we investigated the effects of CNVs on specific cognitive abilities. We examined the burden of large and rare CNVs (>200 kb, <1% MAF) as well as known schizophrenia-associated CNVs in patients with psychotic disorders, their unaffected relatives and controls (N = 3428) from the Psychosis Endophenotypes International Consortium (PEIC). The carriers of specific schizophrenia-associated CNVs showed poorer performance than non-carriers in immediate (P = 0.0036) and delayed (P = 0.0115) verbal recall. We found suggestive evidence that carriers of schizophrenia-associated CNVs had poorer block design performance (P = 0.0307). We do not find any association between CNV burden and cognition. Our findings show that the known high-risk CNVs are not only associated with schizophrenia and other neurodevelopmental disorders, but are also a contributing factor to impairment in cognitive domains such as memory and perceptual reasoning, and act as intermediate biomarkers of disease risk.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-26T17:43:19Z
2021-01-01T00:00:00Z
2021
2022-04-07T13:24:28Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10071/21570
url http://hdl.handle.net/10071/21570
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1359-4184
10.1038/s41380-020-0820-7
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Springer Nature
publisher.none.fl_str_mv Springer Nature
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv mluisa.alvim@gmail.com
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