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Methylation of the AIM2 gene: An epigenetic mediator of PTSD-related inflammation and neuropathology plasma biomarkers.

Authors :
Hawn SE
Neale Z
Wolf EJ
Zhao X
Pierce M
Fein-Schaffer D
Milberg W
McGlinchey R
Logue M
Miller MW
Source :
Depression and anxiety [Depress Anxiety] 2022 Apr; Vol. 39 (4), pp. 323-333. Date of Electronic Publication: 2022 Mar 21.
Publication Year :
2022

Abstract

Background: Posttraumatic stress disorder (PTSD) is associated with inflammation and various forms of chronic disease. The Absent in Melanoma 2 (AIM2) gene has been implicated in mechanisms of inflammation and anxiety, and methylation at a particular locus in this gene (cg10636246) has previously been shown to influence the association between PTSD and elevated C-reactive protein levels in blood.<br />Method: We tested if this association might extend to other indicators of inflammation and to plasma-based measures of neuropathology in a cohort of post-9/11 US military veterans. Using a Bayesian approach, mediation models were tested cross-sectionally (n = 478) and longitudinally (n = 298). Peripheral markers of inflammation and neuropathology were measured with ultra-sensitive Single Molecule Array (Simoa®) technology.<br />Results: Analyses revealed indirect effects of PTSD symptom severity on peripheral indices of both inflammation (interleukin [IL]6, IL-10, tumor necrosis factor-α; indirect standardized [std.] ß range = 0.018-0.023, all p-values adjusted for multiple testing [p <subscript>adj</subscript> ] < 0.05) and neuropathology (neurofilament light [NFL]; indirect std. ß = -0.018, p <subscript>adj</subscript>  = 0.02) via AIM2 methylation. This indirect effect was also evident when predicting IL-10 at a follow-up assessment (indirect std. ß = -0.018, p <subscript>adj</subscript>  = 0.04) controlling for baseline IL-10.<br />Conclusions: Given that AIM2 methylation mediated the association between PTSD symptoms and multiple inflammatory and neuropathology markers, our results suggest that AIM2 methylation may offer clinical utility for indexing risk for adverse health outcomes associated with these peripheral indices of inflammation and neuropathology. Results also suggest a possible shared etiology underlying the frequent co-occurrence of inflammation and neuropathology.<br /> (Published 2022. This article is a U.S. Government work and is in the public domain in the USA.)

Details

Language :
English
ISSN :
1520-6394
Volume :
39
Issue :
4
Database :
MEDLINE
Journal :
Depression and anxiety
Publication Type :
Academic Journal
Accession number :
35312143
Full Text :
https://doi.org/10.1002/da.23247