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      The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response

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          Abstract

          Response to treatment with selective serotonin reuptake inhibitors (SSRIs) varies considerably between patients. The International SSRI Pharmacogenomics Consortium (ISPC) was formed with the primary goal of identifying genetic variation that may contribute to response to SSRI treatment of major depressive disorder. A genome-wide association study of 4-week treatment outcomes, measured using the 17-item Hamilton Rating Scale for Depression (HRSD-17), was performed using data from 865 subjects from seven sites. The primary outcomes were percent change in HRSD-17 score and response, defined as at least 50% reduction in HRSD-17. Data from two prior studies, the Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomics Study (PGRN-AMPS) and the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study, were used for replication, and a meta-analysis of the three studies was performed ( N=2394). Although many top association signals in the ISPC analysis map to interesting candidate genes, none were significant at the genome-wide level and the associations were not replicated using PGRN-AMPS and STAR*D data. Top association results in the meta-analysis of response included single-nucleotide polymorphisms (SNPs) in the HPRTP4 (hypoxanthine phosphoribosyltransferase pseudogene 4)/ VSTM5 (V-set and transmembrane domain containing 5) region, which approached genome-wide significance ( P=5.03E−08) and SNPs 5' upstream of the neuregulin-1 gene, NRG1 ( P=1.20E−06). NRG1 is involved in many aspects of brain development, including neuronal maturation and variations in this gene have been shown to be associated with increased risk for mental disorders, particularly schizophrenia. Replication and functional studies of these findings are warranted.

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          Most cited references40

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          Neuregulin 1 and susceptibility to schizophrenia.

          The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic studies, studies of gene expression in man, and studies of mouse mutants suggest involvement of glutamate and dopamine neurotransmitter systems. However, so far, strong association has not been found between schizophrenia and variants of the genes encoding components of these systems. Here, we report the results of a genomewide scan of schizophrenia families in Iceland; these results support previous work, done in five populations, showing that schizophrenia maps to chromosome 8p. Extensive fine-mapping of the 8p locus and haplotype-association analysis, supplemented by a transmission/disequilibrium test, identifies neuregulin 1 (NRG1) as a candidate gene for schizophrenia. NRG1 is expressed at central nervous system synapses and has a clear role in the expression and activation of neurotransmitter receptors, including glutamate receptors. Mutant mice heterozygous for either NRG1 or its receptor, ErbB4, show a behavioral phenotype that overlaps with mouse models for schizophrenia. Furthermore, NRG1 hypomorphs have fewer functional NMDA receptors than wild-type mice. We also demonstrate that the behavioral phenotypes of the NRG1 hypomorphs are partially reversible with clozapine, an atypical antipsychotic drug used to treat schizophrenia.
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            Prevalence of mental disorders in Europe: results from the European Study of the Epidemiology of Mental Disorders (ESEMeD) project.

            To describe the 12-month and lifetime prevalence rates of mood, anxiety and alcohol disorders in six European countries. A representative random sample of non-institutionalized inhabitants from Belgium, France, Germany, Italy, the Netherlands and Spain aged 18 or older (n = 21425) were interviewed between January 2001 and August 2003. DSM-IV disorders were assessed by lay interviewers using a revised version of the Composite International Diagnostic Interview (WMH-CIDI). Fourteen per cent reported a lifetime history of any mood disorder, 13.6% any anxiety disorder and 5.2% a lifetime history of any alcohol disorder. More than 6% reported any anxiety disorder, 4.2% any mood disorder, and 1.0% any alcohol disorder in the last year. Major depression and specific phobia were the most common single mental disorders. Women were twice as likely to suffer 12-month mood and anxiety disorders as men, while men were more likely to suffer alcohol abuse disorders. ESEMeD is the first study to highlight the magnitude of mental disorders in the six European countries studied. Mental disorders were frequent, more common in female, unemployed, disabled persons, or persons who were never married or previously married. Younger persons were also more likely to have mental disorders, indicating an early age of onset for mood, anxiety and alcohol disorders.
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              MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway.

              Primary microcephaly 1 is a neurodevelopmental disorder caused by mutations in the MCPH1 gene, whose product MCPH1 (also known as microcephalin and BRIT1) regulates DNA-damage response. Here we show that Mcph1 disruption in mice results in primary microcephaly, mimicking human MCPH1 symptoms, owing to a premature switching of neuroprogenitors from symmetric to asymmetric division. MCPH1-deficiency abrogates the localization of Chk1 to centrosomes, causing premature Cdk1 activation and early mitotic entry, which uncouples mitosis and the centrosome cycle. This misorients the mitotic spindle alignment and shifts the division plane of neuroprogenitors, to bias neurogenic cell fate. Silencing Cdc25b, a centrosome substrate of Chk1, corrects MCPH1-deficiency-induced spindle misalignment and rescues the premature neurogenic production in Mcph1-knockout neocortex. Thus, MCPH1, through its function in the Chk1-Cdc25-Cdk1 pathway to couple the centrosome cycle with mitosis, is required for precise mitotic spindle orientation and thereby regulates the progenitor division mode to maintain brain size.
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                Author and article information

                Journal
                Transl Psychiatry
                Transl Psychiatry
                Translational Psychiatry
                Nature Publishing Group
                2158-3188
                April 2015
                21 April 2015
                1 April 2015
                : 5
                : 4
                : e553
                Affiliations
                [1 ]Department of Psychiatry and Psychology, Mayo Clinic , Rochester, MN, USA
                [2 ]Department of Health Sciences Research, Mayo Clinic , Rochester, MN, USA
                [3 ]Department of Genetics, Stanford University , Stanford, CA, USA
                [4 ]Department of Bioengineering, Stanford University , Stanford, CA, USA
                [5 ]Department of Psychiatry and Psychotherapy, University of Muenster , Muenster, Germany
                [6 ]Department of Clinical Pharmacology, University Göttingen , Göttingen, Germany
                [7 ]Department of Psychiatry, Taipei Medical University-Shuangho Hospital , New Taipei City, Taiwan
                [8 ]Department of Psychiatry, Psychosomatics and Psychotherapy, University of Wuerzburg , Wuerzburg, Germany
                [9 ]Department of Psychiatry, Taipei Veterans General Hospital , Taipei, Taiwan
                [10 ]Division of Psychiatry, School of Medicine, National Yang-Ming University , Taipei, Taiwan
                [11 ]Department of Psychiatry, School of Medicine, University of Tampere , Tampere, Finland
                [12 ]Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic , Rochester, MN, USA
                [13 ]Department of Psychiatry, Seinäjoki Hospital District , Seinäjoki, Finland
                [14 ]Department of Neuropsychiatry, Kansai Medical University , Osaka, Japan
                [15 ]Department of Psychiatry, Tampere University Hospital , Tampere, Finland
                [16 ]RIKEN Center for Integrative Medical Sciences , Kanagawa, Japan
                [17 ]Department of Pharmacy, Hyogo University of Health Sciences , Hyogo, Japan
                [18 ]Department of Psychiatry, University of Adelaide , Adelaide, SA, Australia
                [19 ]Center for Neuropsychiatric Research, National Health Research Institutes , Miaoli, Taiwan
                [20 ]Center for Medical Genetics Research, Rajanukul Institute, Department of Mental Health, Ministry of Public Health Bangkok , Bangkok, Thailand
                [21 ]Research Division Federal Institute for Drugs and Medical Devices , Bonn, Germany
                Author notes
                [* ]Department of Psychiatry and Psychology, Mayo Clinic , 200 First Street SW, Rochester, MN 55905, USA. E-mail: biernacka.joanna@ 123456mayo.edu
                Article
                tp201547
                10.1038/tp.2015.47
                4462610
                25897834
                33b6bf16-2cb1-49a4-adff-415d14cc990f
                Copyright © 2015 Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 13 February 2015
                : 01 March 2015
                Categories
                Original Article

                Clinical Psychology & Psychiatry
                Clinical Psychology & Psychiatry

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