Research Letter: PTSD has shared polygenic contributions with bipolar disorder and schizophrenia in women

Twin studies have demonstrated overlap between genetic contributions to post-traumatic stress disorder (PTSD) and other psychiatric disorders (Kremen et al. 2012). These findings have prompted interest in examining shared genetic risk between PTSD and other psychopathology at the molecular level. Wi...

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Published in:Psychological medicine Vol. 46; no. 3; pp. 669 - 671
Main Authors: Sumner, J. A., Duncan, L., Ratanatharathorn, A., Roberts, A. L., Koenen, K. C.
Format: Journal Article
Language:English
Published: Cambridge Cambridge University Press 01.02.2016
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ISSN:0033-2917, 1469-8978
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Abstract Twin studies have demonstrated overlap between genetic contributions to post-traumatic stress disorder (PTSD) and other psychiatric disorders (Kremen et al. 2012). These findings have prompted interest in examining shared genetic risk between PTSD and other psychopathology at the molecular level. With genome-wide association studies (GWAS) and collaborative consortia-based efforts, replicable risk variants have been identified for schizophrenia and bipolar disorder (Cross-Disorder Group of the Psychiatric Genomics Consortium, 2013; Schizophrenia Working Group of the Psychiatric Genomics Consortium, 2014). Analyses of genetic loci in aggregate (polygenic effects; Purcell et al. 2009) have demonstrated shared genetic risk between schizophrenia, bipolar disorder, and major depressive disorder (MDD), with greatest overlap for schizophrenia and bipolar disorder (Cross-Disorder Group of the Psychiatric Genomics Consortium, 2013). Using 3742 candidate single nucleotide polymorphisms (SNPs), an initial polygenic analysis of PTSD by our group (Solovieff et al. 2014) suggested overlap in genetic risk for bipolar disorder and PTSD in European American (EA) women that was replicated in a male EA sample with genome-wide data (Nievergelt et al. 2015).
AbstractList Twin studies have demonstrated overlap between genetic contributions to post-traumatic stress disorder (PTSD) and other psychiatric disorders (Kremen et al. 2012). These findings have prompted interest in examining shared genetic risk between PTSD and other psychopathology at the molecular level. With genome-wide association studies (GWAS) and collaborative consortia-based efforts, replicable risk variants have been identified for schizophrenia and bipolar disorder (Cross-Disorder Group of the Psychiatric Genomics Consortium, 2013; Schizophrenia Working Group of the Psychiatric Genomics Consortium, 2014). Analyses of genetic loci in aggregate (polygenic effects; Purcell et al. 2009) have demonstrated shared genetic risk between schizophrenia, bipolar disorder, and major depressive disorder (MDD), with greatest overlap for schizophrenia and bipolar disorder (Cross-Disorder Group of the Psychiatric Genomics Consortium, 2013). Using 3742 candidate single nucleotide polymorphisms (SNPs), an initial polygenic analysis of PTSD by our group (Solovieff et al. 2014) suggested overlap in genetic risk for bipolar disorder and PTSD in European American (EA) women that was replicated in a male EA sample with genome-wide data (Nievergelt et al. 2015).
Author Sumner, J. A.
Koenen, K. C.
Duncan, L.
Roberts, A. L.
Ratanatharathorn, A.
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Cites_doi 10.1038/nature13595
10.1016/j.psyneuen.2014.10.017
10.1016/S0140-6736(12)62129-1
10.1038/npp.2014.34
10.1038/nature08185
10.1016/j.neuropharm.2011.03.012
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Snippet Twin studies have demonstrated overlap between genetic contributions to post-traumatic stress disorder (PTSD) and other psychiatric disorders (Kremen et al....
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SubjectTerms Behavior disorders
Bipolar disorder
Consortia
Depression
Epidemiology
Gene loci
Genetic analysis
Genetics
Genomes
Genomics
Hospitals
Mental disorders
Post traumatic stress disorder
Psychopathology
Public health
Schizophrenia
Single-nucleotide polymorphism
Studies
Women
Working groups
Title Research Letter: PTSD has shared polygenic contributions with bipolar disorder and schizophrenia in women
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