Evidence map›Paper›PMID 34715991›Full record

ArticleBiological psychiatry2022

Developmental Timing of Trauma in Women Predicts Unique Extracellular Vesicle Proteome Signatures.

Kathleen E Morrison, Anaïs F Stenson, Ruth Marx-Rattner, Sierra Carter, Vasiliki Michopoulos, Charles F Gillespie, Abigail Powers, Weiliang Huang, Maureen A Kane, Tanja Jovanovic and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2022. 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
2.1field-weighted citation impact, top 12% of its field
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, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
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  6. Merkel cell stimulation in fear and sensory signaling.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  7. Review
  8. Review
  9. Review
  10. The Emerging Role of Brain Mitochondria in Fear and Anxiety.Current topics in behavioral neurosciences · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Kathleen E MorrisonDepartment of Pharmacology and Center for Epigenetic Research in Child Health and Brain Development, University of Maryland School of Medicine, Baltimore, Maryland.
Anaïs F StensonDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University, Detroit, Michigan.
Ruth Marx-RattnerDepartment of Pharmacology and Center for Epigenetic Research in Child Health and Brain Development, University of Maryland School of Medicine, Baltimore, Maryland.
Sierra CarterDepartment of Psychology, Georgia State University, Atlanta, Georgia.
Vasiliki MichopoulosDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia.
Charles F GillespieDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia.
Abigail PowersDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia.
Weiliang HuangDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland.
Maureen A KaneDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland.
Tanja JovanovicDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University, Detroit, Michigan.
Tracy L BaleDepartment of Pharmacology and Center for Epigenetic Research in Child Health and Brain Development, University of Maryland School of Medicine, Baltimore, Maryland. Electronic address: tbale@som.umaryland.edu.
University of Maryland, Baltimore · USEmory University · USWayne State University · USGeorgia State University · US

Funding

Paternal stress epigenetic programming of offspring neurodevelopmentR37MH108286 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2015 to 2024
$6.2M
Impact of Trauma Exposure on Critical Periods in Brain Development and Fear Processing in ChildrenR01MH111682 · NIMH · WAYNE STATE UNIVERSITY · PI JOVANOVIC, TANJA · 2016 to 2020
$3.0M
Placental epigenetic mechanisms contributing to sex-specific impacts of maternal stress on fetal developmentR01HD097093 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI BALE, TRACY L · 2019 to 2023
$2.4M
Female preconception stress programming of offspring neurodevelopmentR01ES028202 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI BALE, TRACY L · 2017 to 2021
$2.2M
Biological Mechanisms of Stress Disorders Co-Morbid with HIV in African American WomenR01MH110364 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOVANOVIC, TANJA, NEIGH, GRETCHEN N · 2016 to 2020
$2.0M
Maternal stress and the vaginal microbiome: impacts on brain developmentR33MH104184 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2016 to 2018
$1.9M
Role of hormonal state in programming effects of peripubertal stress in femalesR00HD091376 · NICHD · WEST VIRGINIA UNIVERSITY · PI MORRISON, KATHLEEN ELIZABETH · 2020 to 2022
$578k
Maternal stress and the vaginal microbiome: impacts on brain developmentR21MH104184 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2014 to 2015
$555k
Neuroimaging correlates of impaired fear inhibition in PTSDR21MH098212 · NIMH · EMORY UNIVERSITY · PI JOVANOVIC, TANJA · 2012 to 2013
$417k
Role of hormonal state in programming effects of peripubertal stress in femalesK99HD091376 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI MORRISON, KATHLEEN ELIZABETH · 2017 to 2018
$251k
NICHD NIH HHS K99 HD091376NICHD NIH HHS R00 HD091376NICHD NIH HHS R01 HD097093NIEHS NIH HHS R01 ES028202NIMH NIH HHS R01 MH110364NIMH NIH HHS R01 MH111682NIMH NIH HHS R21 MH098212NIMH NIH HHS R21 MH104184NIMH NIH HHS R33 MH104184NIMH NIH HHS R37 MH108286
6 · The paper itself

Abstract

backgroundExposure to traumatic events is a risk factor for negative physical and mental health outcomes. However, the underlying biological mechanisms that perpetuate these lasting effects are not known.

methodsWe investigated the impact and timing of sexual trauma, a specific type of interpersonal violence, experienced during key developmental windows of childhood, adolescence, or adulthood on adult health outcomes and associated biomarkers, including circulating cell-free mitochondrial DNA levels and extracellular vesicles (EVs), in a predominantly Black cohort of women (N = 101).

resultsSignificant changes in both biomarkers examined, circulating cell-free mitochondrial DNA levels and EV proteome, were specific to developmental timing of sexual trauma. Specifically, we identified a large number of keratin-related proteins from EVs unique to the adolescent sexual trauma group. Remarkably, the majority of these keratin proteins belong to a 17q21 gene cluster, which suggests a potential local epigenetic regulatory mechanism altered by adolescent trauma to impact keratinocyte EV secretion or its protein cargo. These results, along with changes in fear-potentiated startle and skin conductance detected in these women, suggest that sexual violence experienced during the specific developmental window of adolescence may involve unique programming of the skin, the body's largest stress organ.

conclusionsTogether, these descriptive studies provide novel insight into distinct biological processes altered by trauma experienced during specific developmental windows. Future studies will be required to mechanistically link these biological processes to health outcomes.

Indexed as

Extracellular VesiclesProteomeAdolescentAdultCohort StudiesFemaleHumansViolenceProteomeBiomarkerDevelopmentExtracellular vesicleKeratinProteomicsTrauma

Identifiers

PMID34715991
PMCPMC9219961
OpenAlexW3193983798

What OpenQuestion 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 OpenQuestion graph.