Genomic Approaches to Posttraumatic Stress Disorder: The Psychiatric Genomic Consortium Initiative

被引:33
|
作者
Nievergelt, Caroline M. [1 ,2 ,3 ]
Ashley-Koch, Allison E. [4 ]
Dalvie, Shareefa [11 ]
Hauser, Michael A. [4 ]
Morey, Rajendra A. [5 ,6 ]
Smith, Alicia K. [7 ,8 ]
Uddin, Monica [9 ,10 ]
机构
[1] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Family Med & Publ Hlth, San Diego, CA 92103 USA
[3] Vet Affairs San Diego Healthcare Syst, Ctr Excellence Stress & Mental Hlth, San Diego, CA USA
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[5] Duke Univ, Sch Med, Dept Psychiat & Behav Sci, Durham, NC USA
[6] Durham Vet Affairs Med Ctr, Durham, NC USA
[7] Emory Univ, Dept Gynecol & Obstet, Atlanta, GA 30322 USA
[8] Emory Univ, Dept Psychiat & Behav Sci, Atlanta, GA 30322 USA
[9] Univ Illinois, Carl R Woese Inst Genom Biol, Champaign, IL USA
[10] Univ Illinois, Dept Psychol, Champaign, IL USA
[11] Univ Cape Town, Dept Psychiat & Mental Hlth, Cape Town, South Africa
关键词
Epigenetics; Gene expression; Genetics; Imaging; Psychiatric Genomics Consortium (PGC); Systems biology; DNA METHYLATION AGE; WIDE ASSOCIATION; GENE-EXPRESSION; HIPPOCAMPAL VOLUME; RISK; PTSD; METAANALYSIS; TRAUMA; PROFILES; LOCI;
D O I
10.1016/j.biopsych.2018.01.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Posttraumatic stress disorder (PTSD) after exposure to a traumatic event is a highly prevalent psychiatric disorder. Heritability estimates from twin studies as well as from recent molecular data (single nucleotide polymorphism-based heritability) indicate moderate to high heritability, yet robust genetic variants for PTSD have not yet been identified and the genetic architecture of this polygenic disorder remains largely unknown. To date, fewer than 10 large-scale genome-wide association studies of PTSD have been published, with findings that highlight the unique challenges for PTSD genomics, including a complex diagnostic entity with contingency of PTSD diagnosis on trauma exposure and the large genetic diversity of the study populations. The Psychiatric Genomics Consortium PTSD group has brought together more than 200 scientists with the goal to increase sample size for genome-wide association studies and other genomic analyses to sufficient numbers where robust discoveries of molecular signatures can be achieved. The sample currently includes more than 32,000 PTSD cases and 100,000 trauma-exposed control subjects, and collection is ongoing. The first results found a significant shared genetic risk of PTSD with other psychiatric disorders and sex-biased heritability estimates with higher heritability in female individuals compared with male individuals. This review describes the scope and current focus of the Psychiatric Genomics Consortium PTSD group and its expansion from the initial genome-wide association study group to nine working groups, including epigenetics, gene expression, imaging, and integrative systems biology. We further briefly outline recent findings and future directions of "omics"-based studies of PTSD, with the ultimate goal of elucidating the molecular architecture of this complex disorder to improve prevention and intervention strategies.
引用
收藏
页码:831 / 839
页数:9
相关论文
共 50 条
  • [1] The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration
    Logue, Mark W.
    Amstadter, Ananda B.
    Baker, Dewleen G.
    Duncan, Laramie
    Koenen, Karestan C.
    Liberzon, Israel
    Miller, Mark W.
    Morey, Rajendra A.
    Nievergelt, Caroline M.
    Ressler, Kerry J.
    Smith, Alicia K.
    Smoller, Jordan W.
    Stein, Murray B.
    Sumner, Jennifer A.
    Uddin, Monica
    NEUROPSYCHOPHARMACOLOGY, 2015, 40 (10) : 2287 - 2297
  • [2] The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration
    Mark W Logue
    Ananda B Amstadter
    Dewleen G Baker
    Laramie Duncan
    Karestan C Koenen
    Israel Liberzon
    Mark W Miller
    Rajendra A Morey
    Caroline M Nievergelt
    Kerry J Ressler
    Alicia K Smith
    Jordan W Smoller
    Murray B Stein
    Jennifer A Sumner
    Monica Uddin
    Neuropsychopharmacology, 2015, 40 : 2287 - 2297
  • [3] Genomic approaches to neurological and psychiatric disorders
    Burmeister, M.
    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2010, 13 : 17 - 17
  • [4] Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder
    Mehta, Divya
    Klengel, Torsten
    Conneely, Karen N.
    Smith, Alicia K.
    Altmann, Andre
    Pace, Thaddeus W.
    Rex-Haffner, Monika
    Loeschner, Anne
    Gonik, Mariya
    Mercer, Kristina B.
    Bradley, Bekh
    Mueller-Myhsok, Bertram
    Ressler, Kerry J.
    Binder, Elisabeth B.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (20) : 8302 - 8307
  • [5] Genomic and neuroimaging approaches to bipolar disorder
    Kohshour, Mojtaba Oraki
    Papiol, Sergi
    Ching, Christopher R. K.
    Schulze, Thomas G.
    BJPSYCH OPEN, 2022, 8 (02):
  • [6] SYSTEMS GENOMIC AND FUNCTIONAL APPROACHES TO PSYCHIATRIC DISORDERS
    Brennand, Kristen
    Huckins, Laura
    Koenen, Karestan
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2021, 51 : E28 - E28
  • [7] The First Steps on the Path Toward Genomic Predictors of Behavioral Therapy for Posttraumatic Stress Disorder
    Enoch, Mary-Anne
    BIOLOGICAL PSYCHIATRY, 2013, 73 (11) : 1039 - 1040
  • [8] Posttraumatic Stress Disorder Brain Transcriptomics: Convergent Genomic Signatures Across Biological Sex
    Wang, Jiawei
    Zhao, Hongyu
    Girgenti, Matthew J.
    BIOLOGICAL PSYCHIATRY, 2022, 91 (01) : 6 - 13
  • [9] Genomic approaches to plant stress tolerance
    Cushman, JC
    Bohnert, HJ
    CURRENT OPINION IN PLANT BIOLOGY, 2000, 3 (02) : 117 - 124
  • [10] POSTTRAUMATIC-STRESS-DISORDER - A PSYCHIATRIC DEFENSE
    JORDAN, HW
    HOWE, GL
    GELSOMINO, J
    LOCKERT, EW
    JOURNAL OF THE NATIONAL MEDICAL ASSOCIATION, 1986, 78 (02) : 119 - 126