Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects
Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood. We tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in...
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Published in | Psychological medicine Vol. 52; no. 6; pp. 1069 - 1079 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge, UK
Cambridge University Press
01.04.2022
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Subjects | |
Online Access | Get full text |
ISSN | 0033-2917 1469-8978 1469-8978 |
DOI | 10.1017/S0033291720002822 |
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Abstract | Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood.
We tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in a sample of 623 psychiatrically healthy, non-clinical subjects from the FOR2107 multi-centre study and a second sample of 1133 blood donors.
We did not find correlations of schizophrenia PRS with either overall SPQ or specific dimension scores, nor with adjusted schizotypy scores derived from the SPQ (addressing inter-scale variance). Also, PRS for affective disorders (bipolar disorder and major depression) were not significantly associated with schizotypy.
This important negative finding demonstrates that despite the hypothesised continuum of schizotypy and schizophrenia, schizotypy might share less genetic risk with schizophrenia than previously assumed (and possibly less compared to psychotic-like experiences). |
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AbstractList | Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood.BACKGROUNDSchizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood.We tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in a sample of 623 psychiatrically healthy, non-clinical subjects from the FOR2107 multi-centre study and a second sample of 1133 blood donors.METHODSWe tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in a sample of 623 psychiatrically healthy, non-clinical subjects from the FOR2107 multi-centre study and a second sample of 1133 blood donors.We did not find correlations of schizophrenia PRS with either overall SPQ or specific dimension scores, nor with adjusted schizotypy scores derived from the SPQ (addressing inter-scale variance). Also, PRS for affective disorders (bipolar disorder and major depression) were not significantly associated with schizotypy.RESULTSWe did not find correlations of schizophrenia PRS with either overall SPQ or specific dimension scores, nor with adjusted schizotypy scores derived from the SPQ (addressing inter-scale variance). Also, PRS for affective disorders (bipolar disorder and major depression) were not significantly associated with schizotypy.This important negative finding demonstrates that despite the hypothesised continuum of schizotypy and schizophrenia, schizotypy might share less genetic risk with schizophrenia than previously assumed (and possibly less compared to psychotic-like experiences).CONCLUSIONSThis important negative finding demonstrates that despite the hypothesised continuum of schizotypy and schizophrenia, schizotypy might share less genetic risk with schizophrenia than previously assumed (and possibly less compared to psychotic-like experiences). Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood. We tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in a sample of 623 psychiatrically healthy, non-clinical subjects from the FOR2107 multi-centre study and a second sample of 1133 blood donors. We did not find correlations of schizophrenia PRS with either overall SPQ or specific dimension scores, nor with adjusted schizotypy scores derived from the SPQ (addressing inter-scale variance). Also, PRS for affective disorders (bipolar disorder and major depression) were not significantly associated with schizotypy. This important negative finding demonstrates that despite the hypothesised continuum of schizotypy and schizophrenia, schizotypy might share less genetic risk with schizophrenia than previously assumed (and possibly less compared to psychotic-like experiences). BackgroundSchizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood.MethodsWe tested the hypothesis that dimensions of schizotypy (assessed with the SPQ-B) are associated with a polygenic risk score (PRS) for schizophrenia in a sample of 623 psychiatrically healthy, non-clinical subjects from the FOR2107 multi-centre study and a second sample of 1133 blood donors.ResultsWe did not find correlations of schizophrenia PRS with either overall SPQ or specific dimension scores, nor with adjusted schizotypy scores derived from the SPQ (addressing inter-scale variance). Also, PRS for affective disorders (bipolar disorder and major depression) were not significantly associated with schizotypy.ConclusionsThis important negative finding demonstrates that despite the hypothesised continuum of schizotypy and schizophrenia, schizotypy might share less genetic risk with schizophrenia than previously assumed (and possibly less compared to psychotic-like experiences). |
Author | Forstner, Andreas J. Meller, Tina Heilmann-Heimbach, Stefanie Ettinger, Ulrich Hall, Alisha S. M. Krug, Axel Stein, Frederike Grant, Phillip Witt, Stephanie H. Hahn, Tim Streit, Fabian Andlauer, Till F. M. Meinert, Susanne Ripke, Stephan Brosch, Katharina Rietschel, Marcella Mosebach, Johannes Müller-Myhsok, Bertram Nenadić, Igor Jansen, Andreas Fingas, Stella Awasthi, Swapnil Opel, Nils Lemke, Hannah Dannlowski, Udo Schmitt, Simon Kircher, Tilo Nöthen, Markus M. Förster, Katharina |
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M. surname: Andlauer fullname: Andlauer, Till F. M. organization: 7Max-Planck-Institute of Psychiatry, Kraepelinstr. 2-10, 80804 Munich, Germany – sequence: 17 givenname: Andreas J. surname: Forstner fullname: Forstner, Andreas J. organization: 9Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Venusberg-Campus 1, 53127 Bonn, Germany – sequence: 18 givenname: Stefanie surname: Heilmann-Heimbach fullname: Heilmann-Heimbach, Stefanie organization: 9Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Venusberg-Campus 1, 53127 Bonn, Germany – sequence: 19 givenname: Alisha S. M. surname: Hall fullname: Hall, Alisha S. M. organization: 11Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, J5, 68159 Mannheim, Germany – sequence: 20 givenname: Swapnil surname: Awasthi fullname: Awasthi, Swapnil organization: 12Department of Psychiatry and Psychotherapy, Charité – Universitätsmedizin, Berlin, Germany – sequence: 21 givenname: Stephan surname: Ripke fullname: Ripke, Stephan organization: 12Department of Psychiatry and Psychotherapy, Charité – Universitätsmedizin, Berlin, Germany – sequence: 22 givenname: Stephanie H. surname: Witt fullname: Witt, Stephanie H. organization: 11Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, J5, 68159 Mannheim, Germany – sequence: 23 givenname: Marcella surname: Rietschel fullname: Rietschel, Marcella organization: 11Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, J5, 68159 Mannheim, Germany – sequence: 24 givenname: Bertram surname: Müller-Myhsok fullname: Müller-Myhsok, Bertram organization: 7Max-Planck-Institute of Psychiatry, Kraepelinstr. 2-10, 80804 Munich, Germany – sequence: 25 givenname: Markus M. surname: Nöthen fullname: Nöthen, Markus M. organization: 9Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Venusberg-Campus 1, 53127 Bonn, Germany – sequence: 26 givenname: Udo surname: Dannlowski fullname: Dannlowski, Udo organization: 6Department of Psychiatry and Psychotherapy, Westfälische Wilhelms-Universität Münster, Albert-Schweitzer-Campus 1, Building A9, 48149 Münster, Germany – sequence: 27 givenname: Axel surname: Krug fullname: Krug, Axel organization: 1Department of Psychiatry and Psychotherapy, Philipps-University and University Hospital Marburg, UKGM, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany – sequence: 28 givenname: Fabian surname: Streit fullname: Streit, Fabian organization: 11Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, J5, 68159 Mannheim, Germany – sequence: 29 givenname: Tilo surname: Kircher fullname: Kircher, Tilo organization: 1Department of Psychiatry and Psychotherapy, Philipps-University and University Hospital Marburg, UKGM, Rudolf-Bultmann-Str. 8, 35039 Marburg, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32758327$$D View this record in MEDLINE/PubMed |
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Keywords | major depressive disorder Bipolar disorder depression schizophrenia schizotypy psychosis proneness psychosis |
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Snippet | Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly understood.
We tested... BackgroundSchizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly... Schizotypy is a putative risk phenotype for psychosis liability, but the overlap of its genetic architecture with schizophrenia is poorly... |
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SubjectTerms | Affective disorders Bipolar Disorder Blood & organ donations Blood donors Donors Emotional disorders Genetic susceptibility Genomes Genotype & phenotype Hallucinations Humans Mental disorders Multicenter studies Original Article Personality disorders Phenotype Phenotypes Polygenic inheritance Population Psychosis Psychotic Disorders - psychology Quantitative psychology Questionnaires Schizophrenia Schizophrenia - genetics Schizotypal personality Schizotypal personality disorder Schizotypal Personality Disorder - psychology |
Title | Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects |
URI | https://www.cambridge.org/core/product/identifier/S0033291720002822/type/journal_article https://www.ncbi.nlm.nih.gov/pubmed/32758327 https://www.proquest.com/docview/2673461690 https://www.proquest.com/docview/2431812574 |
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