Posttraumatic Stress Disorder, Obesity, and Epigenetic Aging: A Replication Study in 1828 Veterans.

Biopsychosocial science and medicine Pub Date : 2025-07-01 Epub Date: 2025-05-07 DOI:10.1097/PSY.0000000000001397
Kyle J Bourassa, Melanie E Garrett, Allison E Ashley-Koch, Jean C Beckham, Nathan A Kimbrel
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Abstract

Objective: Posttraumatic stress disorder (PTSD) is associated with poor health, and prior research suggests that accelerated epigenetic aging could help explain this association. A recent study found that veterans with both PTSD and obesity had greater risk for accelerated epigenetic aging compared with those with either PTSD or obesity individually, or neither condition. The objective of this study was to conduct a replication and extension of this prior work.

Methods: This study included models approximating the recent study's analytic approach in a sample of 1828 post-9/11 veterans. Our extension also included additional aging measures (PC-GrimAge and DunedinPACE), a more diverse sample, additional covariates (chronological age, smoking), and use of continuous measures of PTSD, obesity, and accelerated aging.

Results: In contrast with the original report, we did not find evidence that obesity moderated the association of PTSD and aging, indicating that veterans with both conditions had greater risk for accelerated aging. Although several significant interactions were observed, they were in the opposite direction of the original study findings (ie, PTSD was more strongly associated with aging scores among veterans with less body mass). Our results instead demonstrated that PTSD was associated with accelerated aging across all continuously measured aging scores (0.08 ≤all βs ≤0.10), and that obesity was associated with faster DunedinPACE aging scores [β=0.36, 95% CI (0.28, 0.44)].

Conclusions: Our findings provide additional evidence that PTSD and obesity may be useful targets for interventions aiming to slow aging and improve health.

创伤后应激障碍、肥胖和表观遗传衰老:1828名退伍军人的重复研究。
目的:创伤后应激障碍(PTSD)与健康状况不佳有关,先前的研究表明,加速的表观遗传衰老可能有助于解释这种关联。最近的一项研究发现,患有创伤后应激障碍和肥胖的退伍军人比那些单独患有创伤后应激障碍或肥胖的退伍军人有更大的加速表观遗传衰老的风险。本研究的目的是对先前的工作进行复制和扩展。方法:本研究在1828名9/11后退伍军人样本中采用了与最近研究的分析方法近似的模型。我们的扩展还包括额外的衰老测量(PC-GrimAge和DunedinPACE),更多样化的样本,额外的协变量(实足年龄,吸烟),以及使用PTSD,肥胖和加速衰老的连续测量。结果:与最初的报告相反,我们没有发现肥胖减缓创伤后应激障碍和衰老的关联的证据,这表明患有这两种疾病的退伍军人加速衰老的风险更大。虽然观察到一些显著的相互作用,但它们与最初的研究结果相反(即,在体重较轻的退伍军人中,PTSD与衰老分数的关系更强)。相反,我们的研究结果表明,在所有连续测量的衰老评分中,PTSD与加速衰老相关(0.08≤所有βs≤0.10),肥胖与更快的DunedinPACE衰老评分相关(β=0.36, 95% CI[0.28, 0.44])。结论:我们的研究结果提供了额外的证据,表明创伤后应激障碍和肥胖可能是旨在延缓衰老和改善健康的干预措施的有用目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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