Evidence map›Paper›PMID 37980332›Full record

ArticleTranslational psychiatry2023

Association between microbiome and the development of adverse posttraumatic neuropsychiatric sequelae after traumatic stress exposure.

Abigail L Zeamer, Marie-Claire Salive, Xinming An, Francesca L Beaudoin, Stacey L House, Jennifer S Stevens, Donglin Zeng, Thomas C Neylan, Gari D Clifford, Sarah D Linnstaedt and 27 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
–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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  12. ACS pharmacology & translational science · 2025
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  18. Social anxiety disorder-associated gut microbiota increases social fear.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

37 authors.

Abigail L ZeamerDepartment of Microbiology and Physiologic Systems, University of Massachusetts Chan Medical School, Worcester, MA, USA.ORCID 0000-0002-3600-4519
Marie-Claire SaliveDepartment of Emergency Medicine, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Xinming AnInstitute for Trauma Recovery, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Francesca L BeaudoinDepartment of Epidemiology, Brown University, Providence, RI, USA.
Stacey L HouseDepartment of Emergency Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Jennifer S StevensDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.ORCID 0000-0003-4674-0314
Donglin ZengDepartment of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC, USA.
Thomas C NeylanDepartments of Psychiatry and Neurology, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-1572-2626
Gari D CliffordDepartment of Biomedical Informatics, Emory University School of Medicine, Atlanta, GA, USA.
Sarah D LinnstaedtInstitute for Trauma Recovery, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0001-5295-7072
Scott L RauchDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Alan B StorrowDepartment of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-2893-808X
Christopher LewandowskiDepartment of Emergency Medicine, Henry Ford Health System, Detroit, MI, USA.ORCID 0000-0001-8297-0024
Paul I MuseyDepartment of Emergency Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Phyllis L HendryDepartment of Emergency Medicine, University of Florida College of Medicine-Jacksonville, Jacksonville, FL, USA.
Sophia SheikhDepartment of Emergency Medicine, University of Florida College of Medicine-Jacksonville, Jacksonville, FL, USA.ORCID 0000-0003-1939-3126
Christopher W JonesDepartment of Emergency Medicine, Cooper Medical School of Rowan University, Camden, NJ, USA.
Brittany E PunchesDepartment of Emergency Medicine, Ohio State University College of Medicine, Columbus, OH, USA.ORCID 0000-0002-7546-1966
Robert A SworDepartment of Emergency Medicine, Oakland University William Beaumont School of Medicine, Rochester, MI, USA.
Lauren A HudakDepartment of Emergency Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Jose L PascualDepartment of Surgery, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-1613-7912
Mark J SeamonDepartment of Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Erica HarrisDepartment of Emergency Medicine, Einstein Medical Center, Philadelphia, PA, USA.
Claire PearsonDepartment of Emergency Medicine, Wayne State University, Ascension St. John Hospital, Detroit, MI, USA.
David A PeakDepartment of Emergency Medicine, Massachusetts General Hospital, Boston, MA, USA.
Roland C MerchantDepartment of Emergency Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Robert M DomeierDepartment of Emergency Medicine, Trinity Health-Ann Arbor, Ypsilanti, MI, USA.
Niels K RathlevDepartment of Emergency Medicine, University of Massachusetts Medical School-Baystate, Springfield, MA, USA.
Brian J O'NeilDepartment of Emergency Medicine, Wayne State University, Detroit Receiving Hospital, Detroit, MI, USA.
Paulina SergotDepartment of Emergency Medicine, McGovern Medical School at UTHealth, Houston, TX, USA.
Leon D SanchezDepartment of Emergency Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0002-8807-0913
Steven E BruceDepartment of Psychological Sciences, University of Missouri - St. Louis, St. Louis, MO, USA.ORCID 0000-0002-5807-4382
Ronald C KesslerDepartment of Health Care Policy, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-4831-2305
Karestan C KoenenDepartment of Epidemiology, Harvard University, Boston, MA, USA.ORCID 0000-0003-2978-7655
Samuel A McLeanDepartment of Emergency Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0001-9482-3582
Vanni BucciDepartment of Microbiology and Physiologic Systems, University of Massachusetts Chan Medical School, Worcester, MA, USA. vanni.bucci@umassmed.edu.ORCID 0000-0002-3257-2922
John P HaranDepartment of Microbiology and Physiologic Systems, University of Massachusetts Chan Medical School, Worcester, MA, USA. john.haran@umassmed.edu.ORCID 0000-0001-7311-1121

Funding

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
Understanding the Microbiome-gut-brain axisn Alzheimer disease and its Role in Cognitive DeclineRF1AG067483 · NIA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HARAN, JOHN PATRICK · 2020 to 2020
$3.3M
Understanding the Microbiome-gut-brain axisn Alzheimer disease and its Role in Cognitive DeclineR01AG067483 · NIA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI John Patrick Haran · 2024 to 2026
$1.8M
NIA NIH HHS R01 AG067483NIMH NIH HHS U01 MH110925
6 · The paper itself

Abstract

Patients exposed to trauma often experience high rates of adverse post-traumatic neuropsychiatric sequelae (APNS). The biological mechanisms promoting APNS are currently unknown, but the microbiota-gut-brain axis offers an avenue to understanding mechanisms as well as possibilities for intervention. Microbiome composition after trauma exposure has been poorly examined regarding neuropsychiatric outcomes. We aimed to determine whether the gut microbiomes of trauma-exposed emergency department patients who develop APNS have dysfunctional gut microbiome profiles and discover potential associated mechanisms. We performed metagenomic analysis on stool samples (n = 51) from a subset of adults enrolled in the Advancing Understanding of RecOvery afteR traumA (AURORA) study. Two-, eight- and twelve-week post-trauma outcomes for post-traumatic stress disorder (PTSD) (PTSD checklist for DSM-5), normalized depression scores (PROMIS Depression Short Form 8b) and somatic symptom counts were collected. Generalized linear models were created for each outcome using microbial abundances and relevant demographics. Mixed-effect random forest machine learning models were used to identify associations between APNS outcomes and microbial features and encoded metabolic pathways from stool metagenomics. Microbial species, including Flavonifractor plautii, Ruminococcus gnavus and, Bifidobacterium species, which are prevalent commensal gut microbes, were found to be important in predicting worse APNS outcomes from microbial abundance data. Notably, through APNS outcome modeling using microbial metabolic pathways, worse APNS outcomes were highly predicted by decreased L-arginine related pathway genes and increased citrulline and ornithine pathways. Common commensal microbial species are enriched in individuals who develop APNS. More notably, we identified a biological mechanism through which the gut microbiome reduces global arginine bioavailability, a metabolic change that has also been demonstrated in the plasma of patients with PTSD.

Indexed as

Gastrointestinal MicrobiomeMicrobiotaStress Disorders, Post-TraumaticAdultBiological AvailabilityFecesHumans

Identifiers

PMID37980332
PMCPMC10657470

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.