A robust coordinated molecular response following trauma promotes recovery and protects against chronic pain and neuropsychiatric symptoms

The biological mechanisms governing recovery versus chronicity of adverse posttraumatic neuropsychiatric sequelae (APNS) remain poorly understood. Here, we characterized longitudinal molecular changes among trauma survivors across ten APNS domains, including pain, anxiety, and depression. Recovery across these diverse clinical outcomes was associated with a shared, temporally coordinated transcriptional signature, characterized by early innate immune activation, subsequent homeostatic and wound-healing processes, and later adaptive immune responses. In contrast, chronic APNS trajectories exhibited limited transcriptional remodeling. We derived and externally validated an RNA-based Recovery Score (RRS) capturing the shared molecular response underlying recovery. Higher RRS was associated with greater clinical recovery, elevated peritraumatic cortisol, and lower cumulative stress exposure. Drug-response profiling identified candidate compounds predicted to mimic recovery-associated transcriptional changes. Together, these findings support posttraumatic recovery as an active biological process and identify shared molecular pathways that may be harnessed to prevent multiple adverse posttraumatic outcomes.

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Publication Details

Journal
medRxiv
Published
2026-11-09
DOI
https://doi.org/10.64898/2026.11.07.26367466
Primary Topic
Posttraumatic Stress Disorder Research
Type
preprint
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preprint

A robust coordinated molecular response following trauma promotes recovery and protects against chronic pain and neuropsychiatric symptoms

Christopher Lewandowski, Jennifer Strafford Stevens, Laura Thi Germine, John Patrick Haran et al.
medRxiv
Posttraumatic Stress Disorder Research
preprint

A robust coordinated molecular response following trauma promotes recovery and protects against chronic pain and neuropsychiatric symptoms

Christopher Lewandowski, Jennifer Strafford Stevens, Laura Thi Germine, John Patrick Haran, Stacey L. House, Phyllis L. Hendry, Thomas C. Neylan, Samuel A. McLean, Alan B. Storrow, Ronald C. Kessler, Erica M. Branham, Sarah D. Linnstaedt, Kerry James Ressler, Paul I. Musey, Sophia Sheikh, Natalie Stanley, Francesca L. Beaudoin, Brittanie Winfield, Gari D. Clifford
preprint en

Abstract

The biological mechanisms governing recovery versus chronicity of adverse posttraumatic neuropsychiatric sequelae (APNS) remain poorly understood. Here, we characterized longitudinal molecular changes among trauma survivors across ten APNS domains, including pain, anxiety, and depression. Recovery across these diverse clinical outcomes was associated with a shared, temporally coordinated transcriptional signature, characterized by early innate immune activation, subsequent homeostatic and wound-healing processes, and later adaptive immune responses. In contrast, chronic APNS trajectories exhibited limited transcriptional remodeling. We derived and externally validated an RNA-based Recovery Score (RRS) capturing the shared molecular response underlying recovery. Higher RRS was associated with greater clinical recovery, elevated peritraumatic cortisol, and lower cumulative stress exposure. Drug-response profiling identified candidate compounds predicted to mimic recovery-associated transcriptional changes. Together, these findings support posttraumatic recovery as an active biological process and identify shared molecular pathways that may be harnessed to prevent multiple adverse posttraumatic outcomes.

medRxiv
University of North Carolina at Chapel Hill (US), Albert Einstein College of Medicine (US), Harvard University (US), Johns Hopkins University (US), Emory University (US), Henry Ford Health System (US), University of Massachusetts Chan Medical School (US), University of California, San Francisco (US), Washington University in St. Louis (US), Brown University (US), University of Florida (US), Indiana University School of Medicine (US), University of Florida Health Science Center (US), Vanderbilt University Medical Center (US)
Posttraumatic Stress Disorder Research
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