Accelerated DNA methylation age: Associations with PTSD and neural integrity. (January 2016)

• Record Type: Journal Article
• Authors: Wolf, Erika J.; Logue, Mark W.; Hayes, Jasmeet P.; Sadeh, Naomi; Schichman, Steven A.; Stone, Annjanette; Salat, David H.; Milberg, William; McGlinchey, Regina; Miller, Mark W.
• Is Part Of: Psychoneuroendocrinology. Volume 63(2016:Jan.)
• Page Start: 155
• Page End: 162
• Publication Date: 2016-01
• Subjects: Accelerated aging -- DNA methylation -- PTSD -- Diffusion tensor imaging -- Genu -- Working memory; Psychoneuroendocrinology -- Periodicals; Endocrinology -- Periodicals; Neurology -- Periodicals; Psychiatry -- Periodicals; Neuropsychoendocrinologie -- Périodiques; 616.8
• DOI: 10.1016/j.psyneuen.2015.09.020
• Languages: English
• ISSNs: 0306-4530

Abstract

Highlights: Cellular age can be indexed by DNA methylation and may be advanced relative to chronological age due to environmental factors. Among 281 Iraq/Afghanistan veterans, we found PTSD severity to be associated with accelerated DNA methylation age. Accelerated DNA methylation age was also associated with reduced neural integrity in the genu of the corpus callosum. Accelerated DNA methylation age was indirectly linked to poorer working memory via reduced integrity of the genu. This highlights the clinical significance of PTSD-related accelerated aging with respect to neural integrity and cognition. Abstract: Background: Accumulating evidence suggests that posttraumatic stress disorder (PTSD) may accelerate cellular aging and lead to premature morbidity and neurocognitive decline. Methods: This study evaluated associations between PTSD and DNA methylation (DNAm) age using recently developed algorithms of cellular age by Horvath (2013) and Hannum et al. (2013). These estimates reflect accelerated aging when they exceed chronological age. We also examined if accelerated cellular age manifested in degraded neural integrity, indexed via diffusion tensor imaging. Results: Among 281 male and female veterans of the conflicts in Iraq and Afghanistan, DNAm age was strongly related to chronological age ( r s ∼.88). Lifetime PTSD severity was associated with Hannum DNAm age estimates residualized for chronological age ( β = .13, p = .032). Advanced DNAm age was associated with reduced integrity in the genu of the corpus callosum ( β = −.17, p = .009) and indirectly linked to poorer working memory performance via this region (indirect β = −.05, p = .029). Horvath DNAm age estimates were not associated with PTSD or neural integrity. Conclusions: Results provide novel support for PTSD-related accelerated aging in DNAm and extend the evidence base of known DNAm age correlates to the domains of neural integrity and cognition.