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Glial suppression and post-traumatic stress disorder: A cross-sectional study of 1,520 world trade center responders.
- Source :
-
Brain, behavior, & immunity - health [Brain Behav Immun Health] 2023 May 13; Vol. 30, pp. 100631. Date of Electronic Publication: 2023 May 13 (Print Publication: 2023). - Publication Year :
- 2023
-
Abstract
- Background: Chronically re-experiencing the memory of a traumatic event might cause a glial response. This study examined whether glial activation would be associated with PTSD in a study of responders present after the 9/11 World Trade Center attacks without comorbid cerebrovascular disease.<br />Methods: Plasma was retrieved from 1,520 WTC responders and stored for a cross-sectional sample of responders of varying levels of exposure and PTSD. Plasma levels (pg/ml) of glial fibrillary acidic protein (GFAP) were assayed. Because stroke and other cerebrovascular diseases cause distributional shifts in GFAP levels, multivariable-adjusted finite mixture models analyzed GFAP distributions in responders with and without possible cerebrovascular disease.<br />Results: Responders were aged 56.3 years and primarily male; 11.07% (n = 154) had chronic PTSD. Older age was associated with increased GFAP, whereas higher body mass was associated with decreased GFAP. Multivariable-adjusted finite mixture models revealed that severe re-experiencing trauma from 9/11 was associated with lower GFAP (B = -0.558, p = 0.003).<br />Conclusion: This study presents evidence of reduced plasma GFAP levels among WTC responders with PTSD. Results suggest re-experiencing traumatic events might cause glial suppression.<br />Competing Interests: This is an epidemiological study examining biomarkers associated with posttraumatic stress disorder. The authors have no conflicts of interest to disclose.<br /> (© 2023 The Authors.)
Details
- Language :
- English
- ISSN :
- 2666-3546
- Volume :
- 30
- Database :
- MEDLINE
- Journal :
- Brain, behavior, & immunity - health
- Publication Type :
- Academic Journal
- Accession number :
- 37251545
- Full Text :
- https://doi.org/10.1016/j.bbih.2023.100631