4.7 Article

Attachment Style Moderates Polygenic Risk for Posttraumatic Stress in United States Military Veterans: Results From the National Health and Resilience in Veterans Study

Journal

BIOLOGICAL PSYCHIATRY
Volume 89, Issue 9, Pages 878-887

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2020.09.018

Keywords

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Funding

  1. U.S. Department of Veterans Affairs National Center for Posttraumatic Stress Disorder

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The study found that attachment style may moderate the expression of PTSD symptoms related to polygenic risk, with a positive correlation between re-experiencing PRS and PTSD symptoms observed only among veterans with an insecure attachment style. The research also revealed a significant interaction between attachment style and a novel locus implicated in regulating excitatory synaptic transmission and plasticity.
BACKGROUND: A polygenic risk score (PRS) derived from genome-wide association studies of posttraumatic stress disorder (PTSD) may inform risk for this disorder. To date, however, no known study has examined whether social environmental factors such as attachment style may moderate the relation between PRS and PTSD. METHODS: We evaluated main and interactive effects of PRS and attachment style on PTSD symptoms in a nationally representative sample of trauma-exposed European-American U.S. military veterans (N = 2030). PRS was derived from a genome-wide association study of PTSD re-experiencing symptoms (N = 146,660) in the Million Veteran Program cohort. Using one-sample Mendelian randomization with data from the UK Biobank (N = 115,099), we evaluated the effects of re-experiencing PRS and attachment style on PTSD symptoms. RESULTS: Higher re-experiencing PRS and secure attachment style were independently associated with PTSD symptoms. A significant PRS-by-attachment style interaction was also observed (b = -.11, p = .006), with a positive association between re-experiencing PRS and PTSD symptoms observed only among veterans with an insecure attachment style. One-sample Mendelian randomization analyses suggested that the association between PTSD symptoms and attachment style is bidirectional. PRS enrichment analyses revealed a significant interaction between attachment style and a variant mapping to the IGSF11 gene (rs151177743, p = 2.1 3 10-7), which is implicated in regulating excitatory synaptic transmission and plasticity. CONCLUSIONS: Attachment style may moderate polygenic risk for PTSD symptoms, and a novel locus implicated in synaptic transmission and plasticity may serve as a possible biological mediator of this association. These findings may help inform interpersonally oriented treatments for PTSD for individuals with high polygenic risk for this disorder.

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