Abstract

BackgroundLongitudinal studies of posttraumatic stress (PTS) have documented environmental factors as predictors of trajectories of higher, versus lower, symptoms, among them experiences of childhood physical abuse. Although it is now well-accepted that genes and environments jointly shape the risk of PTS, no published studies have investigated genes, or gene-by-environment interactions (GxEs), as predictors of PTS trajectories. The purpose of this study was to fill this gap.Methods and MaterialsWe examined associations between variants of the retinoid-related orphan receptor alpha (RORA) gene and trajectory membership among a sample of predominantly non-Hispanic Black urban adults (N = 473). The RORA gene was selected based on its association with posttraumatic stress disorder (PTSD) in the first PTSD genome wide association study. Additionally, we explored GxEs between RORA variants and childhood physical abuse history.ResultsWe found that the minor allele of the RORA SNP rs893290 was a significant predictor of membership in a trajectory of consistently high PTS, relatively to a trajectory of consistently low PTS. Additionally, the GxE of rs893290 with childhood physical abuse was significant. Decomposition of the interaction showed that minor allele frequency was more strongly associated with membership in consistently high or decreasing PTS trajectories, relative to a consistently low PTS trajectory, among participants with higher levels of childhood physical abuse.ConclusionThe results of the study provide preliminary evidence that variation in the RORA gene is associated with membership in trajectories of higher PTS and that these associations are stronger among persons exposed to childhood physical abuse. Replication and analysis of functional data are needed to further our understanding of how RORA relates to PTS trajectories.

Highlights

  • Posttraumatic stress disorder (PTSD) is a debilitating mental disorder characterized by traumatic intrusions, experiential and behavioral avoidance, emotional numbing, and hyperarousal (American Psychological Association 2013)

  • We focus on receptor alpha (RORA) because variants of this gene reached genome wide significance in a prior study, and selected two SNPs that were previously shown to predict posttraumatic stress disorder (PTSD) in our sample, rs16942669 and rs893290 (Logue et al 2010)

  • The results of the study provide preliminary evidence that variation in the RORA gene is associated with membership in trajectories of higher posttraumatic stress (PTS) and that these associations are stronger among persons exposed to childhood physical abuse

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Summary

Introduction

Posttraumatic stress disorder (PTSD) is a debilitating mental disorder characterized by traumatic intrusions, experiential and behavioral avoidance, emotional numbing, and hyperarousal (American Psychological Association 2013). Among persons who do not initially develop PTSD, some continue to experience few or no symptoms, whereas others exhibit a delayed response, meeting criteria for the disorder months or years after the traumatic event (Norris et al 2009). Given these observations, recent studies have explored longitudinal trajectories of PTS, documenting the relative frequency and a 2015 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. Longitudinal studies of posttraumatic stress (PTS) have documented environmental factors as predictors of trajectories of higher, versus lower, symptoms, among them experiences of childhood physical abuse. Replication and analysis of functional data are needed to further our understanding of how RORA relates to PTS trajectories

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