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Polygenic dissection of the bipolar phenotype

Background Recent data provide strong support for a substantial common polygenic contribution (i.e. many alleles each of small effect) to genetic susceptibility for schizophrenia and overlapping susceptibility for bipolar disorder. Aims To test hypotheses about the relationship between schizophrenia...

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Autores principales: Hamshere, M. L., O’Donovan, M. C., Jones, I. R., Jones, L., Kirov, G., Green, E. K., Moskvina, V., Grozeva, D., Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Sklar, P., Purcell, S., Holmans, P. A., Owen, M. J., Craddock, N.
Formato: Texto
Lenguaje:English
Publicado: Royal College Of Psychiatrists 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065773/
https://www.ncbi.nlm.nih.gov/pubmed/21972277
http://dx.doi.org/10.1192/bjp.bp.110.087866
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author Hamshere, M. L.
O’Donovan, M. C.
Jones, I. R.
Jones, L.
Kirov, G.
Green, E. K.
Moskvina, V.
Grozeva, D.
Bass, N.
McQuillin, A.
Gurling, H.
St Clair, D.
Young, A. H.
Ferrier, I. N.
Farmer, A.
McGuffin, P.
Sklar, P.
Purcell, S.
Holmans, P. A.
Owen, M. J.
Craddock, N.
author_facet Hamshere, M. L.
O’Donovan, M. C.
Jones, I. R.
Jones, L.
Kirov, G.
Green, E. K.
Moskvina, V.
Grozeva, D.
Bass, N.
McQuillin, A.
Gurling, H.
St Clair, D.
Young, A. H.
Ferrier, I. N.
Farmer, A.
McGuffin, P.
Sklar, P.
Purcell, S.
Holmans, P. A.
Owen, M. J.
Craddock, N.
author_sort Hamshere, M. L.
collection PubMed
description Background Recent data provide strong support for a substantial common polygenic contribution (i.e. many alleles each of small effect) to genetic susceptibility for schizophrenia and overlapping susceptibility for bipolar disorder. Aims To test hypotheses about the relationship between schizophrenia and psychotic types of bipolar disorder. Method Using a polygenic score analysis to test whether schizophrenia polygenic risk alleles, en masse, significantly discriminate between individuals with bipolar disorder with and without psychotic features. The primary sample included 1829 participants with bipolar disorder and the replication sample comprised 506 people with bipolar disorder. Results The subset of participants with Research Diagnostic Criteria schizoaffective bipolar disorder (n = 277) were significantly discriminated from the remaining participants with bipolar disorder (n = 1552) in both the primary (P = 0.00059) and the replication data-sets (P = 0.0070). In contrast, those with psychotic bipolar disorder as a whole were not significantly different from those with non-psychotic bipolar disorder in either data-set. Conclusions Genetic susceptibility influences at least two major domains of psychopathological variation in the schizophrenia–bipolar disorder clinical spectrum: one that relates to expression of a ‘bipolar disorder-like’ phenotype and one that is associated with expression of ‘schizophrenia-like’ psychotic symptoms.
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spelling pubmed-30657732011-04-07 Polygenic dissection of the bipolar phenotype Hamshere, M. L. O’Donovan, M. C. Jones, I. R. Jones, L. Kirov, G. Green, E. K. Moskvina, V. Grozeva, D. Bass, N. McQuillin, A. Gurling, H. St Clair, D. Young, A. H. Ferrier, I. N. Farmer, A. McGuffin, P. Sklar, P. Purcell, S. Holmans, P. A. Owen, M. J. Craddock, N. Br J Psychiatry Papers Background Recent data provide strong support for a substantial common polygenic contribution (i.e. many alleles each of small effect) to genetic susceptibility for schizophrenia and overlapping susceptibility for bipolar disorder. Aims To test hypotheses about the relationship between schizophrenia and psychotic types of bipolar disorder. Method Using a polygenic score analysis to test whether schizophrenia polygenic risk alleles, en masse, significantly discriminate between individuals with bipolar disorder with and without psychotic features. The primary sample included 1829 participants with bipolar disorder and the replication sample comprised 506 people with bipolar disorder. Results The subset of participants with Research Diagnostic Criteria schizoaffective bipolar disorder (n = 277) were significantly discriminated from the remaining participants with bipolar disorder (n = 1552) in both the primary (P = 0.00059) and the replication data-sets (P = 0.0070). In contrast, those with psychotic bipolar disorder as a whole were not significantly different from those with non-psychotic bipolar disorder in either data-set. Conclusions Genetic susceptibility influences at least two major domains of psychopathological variation in the schizophrenia–bipolar disorder clinical spectrum: one that relates to expression of a ‘bipolar disorder-like’ phenotype and one that is associated with expression of ‘schizophrenia-like’ psychotic symptoms. Royal College Of Psychiatrists 2011-04 /pmc/articles/PMC3065773/ /pubmed/21972277 http://dx.doi.org/10.1192/bjp.bp.110.087866 Text en Royal College of Psychiatrists This paper accords with the Wellcome Trust Open Access policy and is governed by the licence available at http://www.rcpsych.ac.uk/pdf/Wellcome%20Trust%20licence.pdf
spellingShingle Papers
Hamshere, M. L.
O’Donovan, M. C.
Jones, I. R.
Jones, L.
Kirov, G.
Green, E. K.
Moskvina, V.
Grozeva, D.
Bass, N.
McQuillin, A.
Gurling, H.
St Clair, D.
Young, A. H.
Ferrier, I. N.
Farmer, A.
McGuffin, P.
Sklar, P.
Purcell, S.
Holmans, P. A.
Owen, M. J.
Craddock, N.
Polygenic dissection of the bipolar phenotype
title Polygenic dissection of the bipolar phenotype
title_full Polygenic dissection of the bipolar phenotype
title_fullStr Polygenic dissection of the bipolar phenotype
title_full_unstemmed Polygenic dissection of the bipolar phenotype
title_short Polygenic dissection of the bipolar phenotype
title_sort polygenic dissection of the bipolar phenotype
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065773/
https://www.ncbi.nlm.nih.gov/pubmed/21972277
http://dx.doi.org/10.1192/bjp.bp.110.087866
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