Evidence map›Paper›PMID 42856559›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Epigenetic age acceleration is associated with brain connectivity changes and the risk of major depression after trauma.

Alba Navarro-Flores, Hazel Milla, Sarah D Linnstaedt, Xinming An, Jennifer S Stevens, Laura Huff, Nathaniel G Harnett, Alyssa R Roeckner, Katelyn I Oliver, David R Rubinow and 6 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Alba Navarro-FloresMax-Planck-Institute of Psychiatry, Munich, 80804, Germany.
Hazel MillaDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0009-0001-8830-6869
Sarah D LinnstaedtInstitute for Trauma Recovery, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Xinming AnInstitute for Trauma Recovery, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Jennifer S StevensDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Laura HuffDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Nathaniel G HarnettDepartment of Psychiatry, McLean Hospital, Harvard Medical School, Boston, MA, USA.
Alyssa R RoecknerDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Katelyn I OliverDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
David R RubinowDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Karestan C KoenenDepartment of Epidemiology, Harvard School of Public Health, Harvard University, Boston, MA, USA.
Urs HeilbronnerInstitute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Thomas G SchulzeInstitute of Psychiatric Phenomics and Genomics (IPPG), LMU University Hospital, LMU Medizin, Ludwig-Maximilians-Universität München, Munich, Germany.
Kerry J ResslerDepartment of Psychiatry, McLean Hospital, Harvard Medical School, Boston, MA, USA.
Samuel A McLeanDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Anthony S ZannasDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Funding

NIMH Center Repository Supporting Stem Cell ResearchU24MH068457 · NIMH · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI BRZUSTOWICZ, LINDA M, KNOWLES, JAMES A · 2003 to 2024
$213.8M
Longitudinal Assessment of Post-traumatic SyndromesU01MH110925 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KESSLER, RONALD C, KOENEN, KARESTAN C · 2016 to 2020
$25.8M
Interplay between biological aging and neuropsychiatric phenotypes after traumaR01AG088241 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Anthony S. Zannas · 2025 to 2026
$1.3M
NIA NIH HHS R01 AG088241NIMH NIH HHS U01 MH110925NIMH NIH HHS U24 MH068457
6 · The paper itself

Abstract

Background: Major depressive disorder (MDD) is associated with brain dysfunction and age-related diseases. Epigenetic clocks based on DNA methylation patterns estimate biological aging and aim to predict morbidity and mortality. Although MDD has been linked to epigenetic age acceleration (EAA) cross-sectionally, it is unknown whether EAA is associated with MDD after trauma. Methods: We included 706 participants (66% non-white, 64% female) from the multi-ancestry AURORA study, enrolled at emergency departments (ED) within 72 hours after trauma, from whom three age-adjusted epigenetic clocks were measured at enrollment: PhenoAge, GrimAge, and DunedinPACE. Functional MRI and assessment for probable MDD were conducted two weeks and six months later, respectively. Logistic and linear regression models tested the association of EAA with MDD and functional neuroimaging endpoints. Results: A total of 660 participants had available assessments of probable MDD six months after trauma, and from those 160 screened positively (24.2%) after trauma. EAA calculated by GrimAge (OR = 1.44, 95% CI = 1.12 - 1.85, p-adj= 0.012) and DunedinPACE (OR = 1.46, 95% CI = 1.15 - 1.85, p-adj = 0.005), but not PhenoAge (p-adj= 0.239), was significantly associated with MDD 6-months after trauma. Associations remained significant after adjusting for additional confounders, including prior trauma and disability (p= 0.008 for GrimAge, p= 0.010 for DunedinPACE). Subgroup analysis based on a median age split revealed these effects were only observed in participants 35 years of age or older. DunedinPACE was significantly associated with altered connectivity of fourteen brain network pairs after FDR correction (n = 217). Conclusions: EAA is associated with a higher risk of MDD after trauma and with concomitant brain connectivity changes. Calculation of GrimAge and DunedinPACE at the time of ED presentation may help recognize patients at risk for MDD, potentially improving personalized care after trauma.

Indexed as

AgingDepressive DisorderEpigeneticsneuroimagingPsychiatryrs-fMRI

Identifiers

PMID42856559
PMCPMC13648693

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