Gene expression in the dorsolateral and ventromedial prefrontal cortices implicates immune-related gene networks in PTSD
Year: 2021
Type: article
Study design: Observational Study
Abstract: Studies evaluating neuroimaging, genetically predicted gene expression, and pre-clinical genetic models of PTSD, have identified PTSD-related abnormalities in the prefrontal cortex (PFC) of the brain, particularly in dorsolateral and ventromedial PFC (dlPFC and vmPFC). In this study, RNA sequencing was used to examine gene expression in the dlPFC and vmPFC using tissue from the VA National PTSD Brain Bank in donors with histories of PTSD with or without depression (dlPFC n = 38, vmPFC n = 35), depression cases without PTSD (n = 32), and psychopathology-free controls (dlPFC n = 24, vmPFC n = 20). Analyses compared PTSD cases to controls. Follow-up analyses contrasted depression cases to controls. Twenty-one genes were differentially expressed in PTSD after strict multiple testing correction. PTSD-associated genes with roles in learning and memory (FOS, NR4A1), immune regulation (CFH, KPNA1) and myelination (MBP, MOBP, ERMN) were identified. PTSD-associated genes partially overlapped depression-associated genes. Co-expression network analyses identified PTSD-associated networks enriched for immune-related genes across the two brain regions. However, the immune-related genes and association patterns were distinct. The immune gene IL1B was significantly associated with PTSD in candidate-gene analysis and was an upstream regulator of PTSD-associated genes in both regions. There was evidence of replication of dlPFC associations in an independent cohort from a recent study, and a strong correlation between the dlPFC PTSD effect sizes for significant genes in the two studies (r = 0.66, p < 2.2 × 10−16). In conclusion, this study identified several novel PTSD-associated genes and brain region specific PTSD-associated immune-related networks.
Source: Neurobiology of Stress
Institutions: Boston University, VA Boston Healthcare System, Broad Institute, Harvard University, McLean Hospital, Stanley Center for Psychiatric Research, Yale University, VA Connecticut Healthcare System, Texas A&M University, Central Texas Veterans Health Care System, Duke University, Durham VA Health Care System, Duke Medical Center, Brigham and Women's Hospital
Language: English
Subfield: Clinical Psychology
Field: Psychology
Domain: Social Sciences
Open Access status: gold
Estimated APC paid: $3,290
Funders: U.S. Department of Veterans Affairs, McLean Hospital, Harvard Catalyst, National Alliance for Research on Schizophrenia and Depression, National Center for PTSD, U.S. Department of Veterans Affairs, National Institute on Aging, National Institute of Mental Health, National Center for Advancing Translational Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1044962639, G1715169443, G1717162763, G1959896258, G2032961523, G2082041250, G2275923806, PTSD-Related Accelerated Aging in DNA Methylation and Risk for Metabolic Syndrome, G4787961582, G498997782, G5294092380, G6050483719, Neuroimaging Genetics of PTSD, G7627697644, G7644966557, G7984902594, G8455737738, Postdoctoral Training Program in Stress and Trauma
OpenAlex ID: W3201208303
